A new tool for genetically engineering the oldest branch of life – Phys.Org

March 8, 2017 G. William Arends Professor of Microbiology and theme leader of the IGB's Mining Microbial Genomes theme Bill Metcalf, left, with IGB Fellow Dipti Nayak. Credit: University of Illinois at Urbana-Champaign

A new study by G. William Arends Professor of Microbiology at the University of Illinois Bill Metcalf with postdoctoral Fellow Dipti Nayak has documented the use of CRISPR-Cas9 mediated genome editing in the third domain of life, Archaea, for the first time. Their groundbreaking work, reported in Proceedings of the National Academy of Sciences, has the potential to vastly accelerate future studies of these organisms, with implications for research including global climate change. Metcalf and Nayak are members of the Carl R. Woese Institute for Genomic Biology at Illinois.

"Under most circumstances our model archaeon, Methanosarcina acetivorans, has a doubling time of eight to ten hours, as compared to E. coli, which can double in about 30 minutes. What that means is that doing genetics, getting a mutant, can take monthsthe same thing would take three days in E. coli," explains Nayak. "What CRISPR-Cas9 enables us to do, at a very basic level, is speed up the whole process. It removes a major bottleneck... in doing genetics research with this archaeon.

"Even more," continues Nayak, "with our previous techniques, mutations had to be introduced one step at a time. Using this new technology, we can introduce multiple mutations at the same time. We can scale up the process of mutant generation exponentially with CRISPR."

CRISPR, short for Clustered Regularly Interspaced Short Palindromic Repeats, began as an immune defense system in archaea and bacteria. By identifying and storing short fragments of foreign DNA, Cas (CRISPR-associated system) proteins are able to quickly identify that DNA in the future, so that it can then quickly be destroyed, protecting the organism from viral invasion.

Since its discovery, a version of this immune systemCRISPR-Cas9has been modified to edit genomes in the lab. By pairing Cas9 with a specifically engineered RNA guide rather than a fragment of invasive DNA, the CRISPR system can be directed to cut a cell's genome in an arbitrary location such that existing genes can be removed or new ones added. This system has been prolifically useful in editing eukaryotic systems from yeast, to plant, to fish and even human cells, earning it the American Association for the Advancement of Science's 2015 Breakthrough of the Year award. However, its implementation in prokaryotic species has been met with hurdles, due in part to their different cellular processes.

To use CRISPR in a cellular system, researchers have to develop a protocol that takes into account a cell's preferred mechanism of DNA repair: after CRISPR's "molecular scissors" cut the chromosome, the cell's repair system steps in to mend the damage through a mechanism that can be harnessed to remove or add additional genetic material. In eukaryotic cells, this takes the form of Non-Homologous End Joining (NHEJ). Though this pathway has been used for CRISPR-mediated editing, it has the tendency to introduce genetic errors during its repair process: nucleotides, the rungs of the DNA ladder, are often added or deleted at the cut site.

NHEJ is very uncommon in prokaryotes, including Archaea; instead, their DNA is more often repaired through a process known as homology-directed repair. By comparing the damage to a DNA template, homology-directed repair creates what Nayak calls a "deterministic template"the end result can be predicted in advance and tailored to the exact needs of the researcher.

In many ways, homology-directed repair is actually preferable for genome editing: "As much as we want CRISPR-Cas9 to make directed edits in eukaryotic systems, we often end up with things that we don't want, because of NHEJ," explains Nayak. "In this regard, it was a good thing that most archaeal strains don't have a non-homologous end joining repair system, so the only way DNA can be repaired is through this deterministic homologous repair route."

Though it may seem counter-intuitive, one of Nayak and Metcalf's first uses of CRISPR-Cas9 was to introduce an NHEJ mechanism in Methanosarcina acetivorans. Though generally not preferable for genome editing, says Nayak, NHEJ has one use for which it's superior to homologous repair: "If you just want to delete a gene, if you don't care how ... non-homologous end joining is actually more efficient."

By using the introduced NHEJ repair system to perform what are known as "knock-out" studies, wherein a single gene is removed or silenced to see what changes are produced and what processes that gene might affect, Nayak says that future research will be able to assemble a genetic atlas of M. acetivorans and other archaeal species. Such an atlas would be incredibly useful for a variety of fields of research involving Archaea, including an area of particular interest to the Metcalf lab, climate change.

"Methanosarcina acetivorans is the one of the most genetically tractable archaeal strains," says Nayak. "[Methanogens are] a class of archaea that produce gigatons of this potent greenhouse gas every year, play a keystone role in the global carbon cycle, and therefore contribute significantly to global climate change." By studying the genetics of this and similar organisms, Nayak and Metcalf hope to gain not only a deeper understanding of archaeal genetics, but of their role in broader environmental processes.

In all, this research represents an exciting new direction in studying and manipulating archaea. "We began this research to determine if the use of CRISPR-Cas9 genome editing in archaea was even possible," concludes Nayak. "What we've discovered is that it's not only possible, but it works remarkably well, even as compared to eukaryotic systems."

Explore further: Modifying fat content in soybean oil with the molecular scissors Cpf1

More information: Dipti D. Nayak et al, Cas9-mediated genome editing in the methanogenic archaeon, Proceedings of the National Academy of Sciences (2017). DOI: 10.1073/pnas.1618596114

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A new tool for genetically engineering the oldest branch of life - Phys.Org

A Controversial Study Is Tearing the CRISPR World Apart – Gizmodo

When people talk about the gene-editing technology CRISPR, its usually accompanied by adjectives like revolutionary or world-changing. For this reason, its no surprise that a study out last month questioning just how game-changing the technology really is caused quite a stir.

Its well-known that using CRISPR can sometimes also result in some unintended genomic changes, and scientists have long been working on ways to fine-tune it. But the researchers found that when they had used CRISPR to cure blindness in mice, it had resulted in not just a few but more than a thousand, unintendedoff-target effects.

This finding warns that CRISPR technology must be further tailored, particularly before it is used for human gene therapy, the researchers wrote. The technique has already been used in two human trials in China, and next year one is slated to kick off in the US.

Their finding kicked off a battle for CRISPRs honor, with some researchers speaking out to question the studys methods while others piped up to agree that CRISPR is not yet ready for people.

The first criticism came the day after the study was published, via a comment from a researcher on PubMed who argued careless mistakes and flaws in the methodology cast serious doubts about the results or interpretation, concluding that it was hard to imagine CRISPR-cas9 causes so many [unintended] homozygous deletions in two independent mice.

On social media, scientists raised red flags about basic mistakes, such as misidentifying genes, mislabeling genetic defects, and the small number of animals the researchers had included in their research.

I think the Nature Methods paper was a false alarm on CRISPR induced mutations, the geneticist Eric Topol told Gizmodo. Ironically, the methods used were flawed. While we remain aware of such concerns unintended genomic effects that might occur with editingthat report was off-base.

Scientists from the CRISPR-focused companies Intellia Therapeutics and Editas Medicine sent separate letters to the journal, Nature Methods, chiming in with their own critique.

Based on the information available on the mouse study, the more plausible conclusion is that the genetic differences reflect a normal level of variation between individuals in a colony.

We believe that the conclusions drawn from this study are unsubstantiated by the disclosed experiments as they were designed and carried out, the scientists from Editas wrote. Further, it is impossible to ascribe the observed differences in the subject mice to the effects of CRISPR per se. The genetic differences seen in this comparative analysis were likely present prior to editing with CRISPR.

The study sent the stocks of those two companiesand a third, CRISPR Therapeuticstumbling. Nearly two weeks later, those market prices had still not fully recovered. Some went so far as to call for a retraction.

All of our methods are described in our peer reviewed Correspondence and sopplemental materials in Nature Methods and the raw data have all been publicly deposited, so that others may further learn from our data, one of the authors, Alexander Bassuk, told Gizmodo via email.

Springer Nature, which owns Nature Methods, said that they have received a number of communications regarding the paper and said that it had undergone peer review as all papers in the journal do.

We are carefully considering all concerns that have been raised with us and are discussing them with the authors, a spokesperson said.

On his blog, UC Davis professor Paul Knoepfler asked several scientists about the study and got mixed results. One cited the same flaws in methodology others have brought us. Another posited that it was a good reminder to hunt thoroughly for off-target effects.

Overall, this study adds a bit to the knowledge base, but it has been over-interpreted in the media, Knoepfler concluded. It was unlikely, he wrote, that so many unintended edits were occurring in most research, but it still suggested more studies to investigate the problem are necessary.

This brings us to the one thing that is definitely true: Despite all our recent progress, there is still a lot we dont know about CRISPR. It does indeed allow us to make precise gene edits more easily than ever before, but this ability has limitations that could wind up being disastrous if used in humans, and disappointing when genetically engineering everything else. CRISPR is still a nascent technology, and whether one day it might really be used to cure diseases or create a unicorn, there are still a whole lot of things that need to happen first.

Update: This story has been updated to include comments from one of the study authors, Nature Methods and Eric Topol.

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A Controversial Study Is Tearing the CRISPR World Apart - Gizmodo

Human Genome Project – Wikipedia

The Human Genome Project (HGP) was an international scientific research project with the goal of determining the sequence of nucleotide base pairs that make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and a functional standpoint.[1] It remains the world's largest collaborative biological project.[2] After the idea was picked up in 1984 by the US government when the planning started, the project formally launched in 1990 and was declared complete in 2003. Funding came from the US government through the National Institutes of Health (NIH) as well as numerous other groups from around the world. A parallel project was conducted outside of government by the Celera Corporation, or Celera Genomics, which was formally launched in 1998. Most of the government-sponsored sequencing was performed in twenty universities and research centers in the United States, the United Kingdom, Japan, France, Germany, Canada, and China.[3]

The Human Genome Project originally aimed to map the nucleotides contained in a human haploid reference genome (more than three billion). The "genome" of any given individual is unique; mapping the "human genome" involved sequencing a small number of individuals and then assembling these together to get a complete sequence for each chromosome. The finished human genome is thus a mosaic, not representing any one individual.

The Human Genome Project was a 13-year-long, publicly funded project initiated in 1990 with the objective of determining the DNA sequence of the entire euchromatic human genome within 15 years.[4] In May 1985, Robert Sinsheimer organized a workshop to discuss sequencing the human genome,[5] but for a number of reasons the NIH was uninterested in pursuing the proposal. The following March, the Santa Fe Workshop was organized by Charles DeLisi and David Smith of the Department of Energy's Office of Health and Environmental Research (OHER).[6] At the same time Renato Dulbecco proposed whole genome sequencing in an essay in Science.[7] James Watson followed two months later with a workshop held at the Cold Spring Harbor Laboratory.

The fact that the Santa Fe workshop was motivated and supported by a Federal Agency opened a path, albeit a difficult and tortuous one,[8] for converting the idea into public policy. In a memo to the Assistant Secretary for Energy Research (Alvin Trivelpiece), Charles DeLisi, who was then Director of OHER, outlined a broad plan for the project.[9] This started a long and complex chain of events which led to approved reprogramming of funds that enabled OHER to launch the Project in 1986, and to recommend the first line item for the HGP, which was in President Regan's 1988 budget submission,[8] and ultimately approved by the Congress. Of particular importance in Congressional approval was the advocacy of Senator Peter Domenici, whom DeLisi had befriended.[10] Domenici chaired the Senate Committee on Energy and Natural Resources, as well as the Budget Committee, both of which were key in the DOE budget process. Congress added a comparable amount to the NIH budget, thereby beginning official funding by both agencies.

Alvin Trivelpiece sought and obtained the approval of DeLisi's proposal by Deputy Secretary William Flynn Martin. This chart[11] was used in the spring of 1986 by Trivelpiece, then Director of the Office of Energy Research in the Department of Energy, to brief Martin and Under Secretary Joseph Salgado regarding his intention to reprogram $4 million to initiate the project with the approval of Secretary Herrington. This reprogramming was followed by a line item budget of $16 million in the Reagan Administrations 1987 budget submission to Congress.[12] It subsequently passed both Houses. The Project was planned for 15 years.[13]

Candidate technologies were already being considered for the proposed undertaking at least as early as 1985.[14]

In 1990, the two major funding agencies, DOE and NIH, developed a memorandum of understanding in order to coordinate plans and set the clock for the initiation of the Project to 1990.[15] At that time, David Galas was Director of the renamed Office of Biological and Environmental Research in the U.S. Department of Energys Office of Science and James Watson headed the NIH Genome Program. In 1993, Aristides Patrinos succeeded Galas and Francis Collins succeeded James Watson, assuming the role of overall Project Head as Director of the U.S. National Institutes of Health (NIH) National Center for Human Genome Research (which would later become the National Human Genome Research Institute). A working draft of the genome was announced in 2000 and the papers describing it were published in February 2001. A more complete draft was published in 2003, and genome "finishing" work continued for more than a decade.

The $3-billion project was formally founded in 1990 by the US Department of Energy and the National Institutes of Health, and was expected to take 15 years.[16] In addition to the United States, the international consortium comprised geneticists in the United Kingdom, France, Australia, China and myriad other spontaneous relationships.[17]

Due to widespread international cooperation and advances in the field of genomics (especially in sequence analysis), as well as major advances in computing technology, a 'rough draft' of the genome was finished in 2000 (announced jointly by U.S. President Bill Clinton and the British Prime Minister Tony Blair on June 26, 2000).[18] This first available rough draft assembly of the genome was completed by the Genome Bioinformatics Group at the University of California, Santa Cruz, primarily led by then graduate student Jim Kent. Ongoing sequencing led to the announcement of the essentially complete genome on April 14, 2003, two years earlier than planned.[19][20] In May 2006, another milestone was passed on the way to completion of the project, when the sequence of the last chromosome was published in Nature.[21]

The project was not able to sequence all the DNA found in human cells. It sequenced only "euchromatic" regions of the genome, which make up more than 95% of the genome. The other regions, called "heterochromatic" are found in centromeres and telomeres, and were not sequenced under the project.[22]

The Human Genome Project was declared complete in April 2003. An initial rough draft of the human genome was available in June 2000 and by February 2001 a working draft had been completed and published followed by the final sequencing mapping of the human genome on April 14, 2003. Although this was reported to cover 99% of the euchromatic human genome with 99.99% accuracy, a major quality assessment of the human genome sequence was published on May 27, 2004 indicating over 92% of sampling exceeded 99.99% accuracy which was within the intended goal.[23] Further analyses and papers on the HGP continue to occur.[24]

The sequencing of the human genome holds benefits for many fields, from molecular medicine to human evolution. The Human Genome Project, through its sequencing of the DNA, can help us understand diseases including: genotyping of specific viruses to direct appropriate treatment; identification of mutations linked to different forms of cancer; the design of medication and more accurate prediction of their effects; advancement in forensic applied sciences; biofuels and other energy applications; agriculture, animal husbandry, bioprocessing; risk assessment; bioarcheology, anthropology and evolution. Another proposed benefit is the commercial development of genomics research related to DNA based products, a multibillion-dollar industry.

The sequence of the DNA is stored in databases available to anyone on the Internet. The U.S. National Center for Biotechnology Information (and sister organizations in Europe and Japan) house the gene sequence in a database known as GenBank, along with sequences of known and hypothetical genes and proteins. Other organizations, such as the UCSC Genome Browser at the University of Cali
fornia, Santa Cruz,[25] and Ensembl[26] present additional data and annotation and powerful tools for visualizing and searching it. Computer programs have been developed to analyze the data, because the data itself is difficult to interpret without such programs. Generally speaking, advances in genome sequencing technology have followed Moores Law, a concept from computer science which states that integrated circuits can increase in complexity at an exponential rate.[27] This means that the speeds at which whole genomes can be sequenced can increase at a similar rate, as was seen during the development of the above-mentioned Human Genome Project.

The process of identifying the boundaries between genes and other features in a raw DNA sequence is called genome annotation and is in the domain of bioinformatics. While expert biologists make the best annotators, their work proceeds slowly, and computer programs are increasingly used to meet the high-throughput demands of genome sequencing projects. Beginning in 2008, a new technology known as RNA-seq was introduced that allowed scientists to directly sequence the messenger RNA in cells. This replaced previous methods of annotation, which relied on inherent properties of the DNA sequence, with direct measurement, which was much more accurate. Today, annotation of the human genome and other genomes relies primarily on deep sequencing of the transcripts in every human tissue using RNA-seq. These experiments have revealed that over 90% of genes contain at least one and usually several alternative splice variants, in which the exons are combined in different ways to produce 2 or more gene products from the same locus.[citation needed]

The genome published by the HGP does not represent the sequence of every individual's genome. It is the combined mosaic of a small number of anonymous donors, all of European origin. The HGP genome is a scaffold for future work in identifying differences among individuals. Subsequent projects sequenced the genomes of multiple distinct ethnic groups, though as of today there is still only one "reference genome."[citation needed]

Key findings of the draft (2001) and complete (2004) genome sequences include:

The Human Genome Project was started in 1990 with the goal of sequencing and identifying all three billion chemical units in the human genetic instruction set, finding the genetic roots of disease and then developing treatments. It is considered a Mega Project because the human genome has approximately 3.3 billion base-pairs. With the sequence in hand, the next step was to identify the genetic variants that increase the risk for common diseases like cancer and diabetes.[15][33]

It was far too expensive at that time to think of sequencing patients whole genomes. So the National Institutes of Health embraced the idea for a "shortcut", which was to look just at sites on the genome where many people have a variant DNA unit. The theory behind the shortcut was that, since the major diseases are common, so too would be the genetic variants that caused them. Natural selection keeps the human genome free of variants that damage health before children are grown, the theory held, but fails against variants that strike later in life, allowing them to become quite common. (In 2002 the National Institutes of Health started a $138 million dollar project called the HapMap to catalog the common variants in European, East Asian and African genomes.)[34]

The genome was broken into smaller pieces; approximately 150,000 base pairs in length.[33] These pieces were then ligated into a type of vector known as "bacterial artificial chromosomes", or BACs, which are derived from bacterial chromosomes which have been genetically engineered. The vectors containing the genes can be inserted into bacteria where they are copied by the bacterial DNA replication machinery. Each of these pieces was then sequenced separately as a small "shotgun" project and then assembled. The larger, 150,000 base pairs go together to create chromosomes. This is known as the "hierarchical shotgun" approach, because the genome is first broken into relatively large chunks, which are then mapped to chromosomes before being selected for sequencing.[35][36]

Funding came from the US government through the National Institutes of Health in the United States, and a UK charity organization, the Wellcome Trust, as well as numerous other groups from around the world. The funding supported a number of large sequencing centers including those at Whitehead Institute, the Sanger Centre, Washington University in St. Louis, and Baylor College of Medicine.[16][37]

The United Nations Educational, Scientific and Cultural Organization (UNESCO) served as an important channel for the involvement of developing countries in the Human Genome Project.[38]

In 1998, a similar, privately funded quest was launched by the American researcher Craig Venter, and his firm Celera Genomics. Venter was a scientist at the NIH during the early 1990s when the project was initiated. The $300,000,000 Celera effort was intended to proceed at a faster pace and at a fraction of the cost of the roughly $3 billion publicly funded project. The Celera approach was able to proceed at a much more rapid rate, and at a lower cost than the public project because it relied upon data made available by the publicly funded project.[39]

Celera used a technique called whole genome shotgun sequencing, employing pairwise end sequencing,[40] which had been used to sequence bacterial genomes of up to six million base pairs in length, but not for anything nearly as large as the three billion base pair human genome.

Celera initially announced that it would seek patent protection on "only 200300" genes, but later amended this to seeking "intellectual property protection" on "fully-characterized important structures" amounting to 100300 targets. The firm eventually filed preliminary ("place-holder") patent applications on 6,500 whole or partial genes. Celera also promised to publish their findings in accordance with the terms of the 1996 "Bermuda Statement", by releasing new data annually (the HGP released its new data daily), although, unlike the publicly funded project, they would not permit free redistribution or scientific use of the data. The publicly funded competitors were compelled to release the first draft of the human genome before Celera for this reason. On July 7, 2000, the UCSC Genome Bioinformatics Group released a first working draft on the web. The scientific community downloaded about 500 GB of information from the UCSC genome server in the first 24 hours of free and unrestricted access.[41]

In March 2000, President Clinton announced that the genome sequence could not be patented, and should be made freely available to all researchers. The statement sent Celera's stock plummeting and dragged down the biotechnology-heavy Nasdaq. The biotechnology sector lost about $50 billion in market capitalization in two days.

Although the working draft was announced in June 2000, it was not until February 2001 that Celera and the HGP scientists published details of their drafts. Special issues of Nature (which published the publicly funded project's scientific paper)[42] and Science (which published Celera's paper[43]) described the methods used to produce the draft sequence and offered analysis of the sequence. These drafts covered about 83% of the genome (90% of the euchromatic regions with 150,000 gaps and the order and orientation of many segments not yet established). In February 2001, at the time of the joint publications, press releases announced that the project had been completed by both groups. Improved drafts were announced in 2003 and 2005, filling in to approximately 92% of the sequence currently.

In the IHGSC international public-sector Human Genome Project (HGP), researchers collected blood (female) or sperm (male) samples from a large number of donors. Only a few of many collected samples were processed as DNA resources. Thus the donor identities were prot
ected so neither donors nor scientists could know whose DNA was sequenced. DNA clones from many different libraries were used in the overall project, with most of those libraries being created by Pieter J. de Jong's lab. Much of the sequence (>70%) of the reference genome produced by the public HGP came from a single anonymous male donor from Buffalo, New York (code name RP11).[44][45]

HGP scientists used white blood cells from the blood of two male and two female donors (randomly selected from 20 of each) each donor yielding a separate DNA library. One of these libraries (RP11) was used considerably more than others, due to quality considerations. One minor technical issue is that male samples contain just over half as much DNA from the sex chromosomes (one X chromosome and one Y chromosome) compared to female samples (which contain two X chromosomes). The other 22 chromosomes (the autosomes) are the same for both sexes.

Although the main sequencing phase of the HGP has been completed, studies of DNA variation continue in the International HapMap Project, whose goal is to identify patterns of single-nucleotide polymorphism (SNP) groups (called haplotypes, or haps). The DNA samples for the HapMap came from a total of 270 individuals: Yoruba people in Ibadan, Nigeria; Japanese people in Tokyo; Han Chinese in Beijing; and the French Centre dEtude du Polymorphisme Humain (CEPH) resource, which consisted of residents of the United States having ancestry from Western and Northern Europe.

In the Celera Genomics private-sector project, DNA from five different individuals were used for sequencing. The lead scientist of Celera Genomics at that time, Craig Venter, later acknowledged (in a public letter to the journal Science) that his DNA was one of 21 samples in the pool, five of which were selected for use.[46][47]

In 2007, a team led by Jonathan Rothberg published James Watson's entire genome, unveiling the six-billion-nucleotide genome of a single individual for the first time.[48]

The work on interpretation and analysis of genome data is still in its initial stages. It is anticipated that detailed knowledge of the human genome will provide new avenues for advances in medicine and biotechnology. Clear practical results of the project emerged even before the work was finished. For example, a number of companies, such as Myriad Genetics, started offering easy ways to administer genetic tests that can show predisposition to a variety of illnesses, including breast cancer, hemostasis disorders, cystic fibrosis, liver diseases and many others. Also, the etiologies for cancers, Alzheimer's disease and other areas of clinical interest are considered likely to benefit from genome information and possibly may lead in the long term to significant advances in their management.[34][49]

There are also many tangible benefits for biologists. For example, a researcher investigating a certain form of cancer may have narrowed down his/her search to a particular gene. By visiting the human genome database on the World Wide Web, this researcher can examine what other scientists have written about this gene, including (potentially) the three-dimensional structure of its product, its function(s), its evolutionary relationships to other human genes, or to genes in mice or yeast or fruit flies, possible detrimental mutations, interactions with other genes, body tissues in which this gene is activated, and diseases associated with this gene or other datatypes. Further, deeper understanding of the disease processes at the level of molecular biology may determine new therapeutic procedures. Given the established importance of DNA in molecular biology and its central role in determining the fundamental operation of cellular processes, it is likely that expanded knowledge in this area will facilitate medical advances in numerous areas of clinical interest that may not have been possible without them.[50]

The analysis of similarities between DNA sequences from different organisms is also opening new avenues in the study of evolution. In many cases, evolutionary questions can now be framed in terms of molecular biology; indeed, many major evolutionary milestones (the emergence of the ribosome and organelles, the development of embryos with body plans, the vertebrate immune system) can be related to the molecular level. Many questions about the similarities and differences between humans and our closest relatives (the primates, and indeed the other mammals) are expected to be illuminated by the data in this project.[34][51]

The project inspired and paved the way for genomic work in other fields, such as agriculture. For example, by studying the genetic composition of Tritium aestivum, the worlds most commonly used bread wheat, great insight has been gained into the ways that domestication has impacted the evolution of the plant.[52] Which loci are most susceptible to manipulation, and how does this play out in evolutionary terms? Genetic sequencing has allowed these questions to be addressed for the first time, as specific loci can be compared in wild and domesticated strains of the plant. This will allow for advances in genetic modification in the future which could yield healthier, more disease-resistant wheat crops.

At the onset of the Human Genome Project several ethical, legal, and social concerns were raised in regards to how increased knowledge of the human genome could be used to discriminate against people. One of the main concerns of most individuals was the fear that both employers and health insurance companies would refuse to hire individuals or refuse to provide insurance to people because of a health concern indicated by someone's genes.[53] In 1996 the United States passed the Health Insurance Portability and Accountability Act (HIPAA) which protects against the unauthorized and non-consensual release of individually identifiable health information to any entity not actively engaged in the provision of healthcare services to a patient.[54]

Along with identifying all of the approximately 20,00025,000 genes in the human genome, the Human Genome Project also sought to address the ethical, legal, and social issues that were created by the onset of the project. For that the Ethical, Legal, and Social Implications (ELSI) program was founded in 1990. Five percent of the annual budget was allocated to address the ELSI arising from the project.[16][55] This budget started at approximately $1.57 million in the year 1990, but increased to approximately $18 million in the year 2014.[56]

Whilst the project may offer significant benefits to medicine and scientific research, some authors have emphasised the need to address the potential social consequences of mapping the human genome. "Molecularising disease and their possible cure will have a profound impact on what patients expect from medical help and the new generation of doctors' perception of illness."[57]

See more here:
Human Genome Project - Wikipedia

Human – Wikipedia

Human[1] Temporal range: 0.1950Ma Middle Pleistocene Recent An adult human male (left) and female (right) in Northern Thailand. Scientific classification Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Primates Suborder: Haplorhini Family: Hominidae Tribe: Hominini Genus: Homo Species: H.sapiens Binomial name Homo sapiens Linnaeus, 1758 Subspecies

Homo sapiens idaltu White et al., 2003 Homo sapiens sapiens

Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens) are the only extant members of Hominina clade (or human clade), a branch of the taxonomical tribe Hominini belonging to the family of great apes. They are characterized by erect posture and bipedal locomotion; manual dexterity and increased tool use, compared to other animals; and a general trend toward larger, more complex brains and societies.[3][4]

Early homininsparticularly the australopithecines, whose brains and anatomy are in many ways more similar to ancestral non-human apesare less often referred to as "human" than hominins of the genus Homo.[5] Several of these hominins used fire, occupied much of Eurasia, and gave rise to anatomically modern Homo sapiens in Africa about 200,000 years ago.[6][7] They began to exhibit evidence of behavioral modernity around 50,000 years ago. In several waves of migration, anatomically modern humans ventured out of Africa and populated most of the world.[8]

The spread of humans and their large and increasing population has had a profound impact on large areas of the environment and millions of native species worldwide. Advantages that explain this evolutionary success include a relatively larger brain with a particularly well-developed neocortex, prefrontal cortex and temporal lobes, which enable high levels of abstract reasoning, language, problem solving, sociality, and culture through social learning. Humans use tools to a much higher degree than any other animal, are the only extant species known to build fires and cook their food, and are the only extant species to clothe themselves and create and use numerous other technologies and arts.

Humans are uniquely adept at utilizing systems of symbolic communication (such as language and art) for self-expression and the exchange of ideas, and for organizing themselves into purposeful groups. Humans create complex social structures composed of many cooperating and competing groups, from families and kinship networks to political states. Social interactions between humans have established an extremely wide variety of values,[9]social norms, and rituals, which together form the basis of human society. Curiosity and the human desire to understand and influence the environment and to explain and manipulate phenomena (or events) has provided the foundation for developing science, philosophy, mythology, religion, anthropology, and numerous other fields of knowledge.

Though most of human existence has been sustained by hunting and gathering in band societies,[10] increasing numbers of human societies began to practice sedentary agriculture approximately some 10,000 years ago,[11] domesticating plants and animals, thus allowing for the growth of civilization. These human societies subsequently expanded in size, establishing various forms of government, religion, and culture around the world, unifying people within regions to form states and empires. The rapid advancement of scientific and medical understanding in the 19th and 20th centuries led to the development of fuel-driven technologies and increased lifespans, causing the human population to rise exponentially. By February 2016, the global human population had exceeded 7.3 billion.[12]

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In common usage, the word "human" generally refers to the only extant species of the genus Homo anatomically and behaviorally modern Homo sapiens.

In scientific terms, the meanings of "hominid" and "hominin" have changed during the recent decades with advances in the discovery and study of the fossil ancestors of modern humans. The previously clear boundary between humans and apes has blurred, resulting in now acknowledging the hominids as encompassing multiple species, and Homo and close relatives since the split from chimpanzees as the only hominins. There is also a distinction between anatomically modern humans and Archaic Homo sapiens, the earliest fossil members of the species.

The English adjective human is a Middle English loanword from Old French humain, ultimately from Latin hmnus, the adjective form of hom "man." The word's use as a noun (with a plural: humans) dates to the 16th century.[13] The native English term man can refer to the species generally (a synonym for humanity), and could formerly refer to specific individuals of either sex, though this latter use is now obsolete.[14]

The species binomial Homo sapiens was coined by Carl Linnaeus in his 18th century work Systema Naturae.[15] The generic name Homo is a learned 18th century derivation from Latin hom "man," ultimately "earthly being" (Old Latin hem a cognate to Old English guma "man," from PIE demon-, meaning "earth" or "ground").[16] The species-name sapiens means "wise" or "sapient." Note that the Latin word homo refers to humans of either gender, and that sapiens is the singular form (while there is no such word as sapien).[17]

The genus Homo evolved and diverged from other hominins in Africa, after the human clade split from the chimpanzee lineage of the hominids (great apes) branch of the primates. Modern humans, defined as the species Homo sapiens or specifically to the single extant subspecies Homo sapiens sapiens, proceeded to colonize all the continents and larger islands, arriving in Eurasia 125,00060,000 years ago,[18][19]Australia around 40,000 years ago, the Americas around 15,000 years ago, and remote islands such as Hawaii, Easter Island, Madagascar, and New Zealand between the years 300 and 1280.[20][21]

The closest living relatives of humans are chimpanzees (genus Pan) and gorillas (genus Gorilla).[22] With the sequencing of both the human and chimpanzee genome, current estimates of similarity between human and chimpanzee DNA sequences range between 95% and 99%.[22][23][24] By using the technique called a molecular clock which estimates the time required for the number of divergent mutations to accumulate between two lineages, the approximate date for the split between lineages can be calculated. The gibbons (Hylobatidae) and orangutans (genus Pongo) were the first groups to split from the line leading to the humans, then gorillas (genus Gorilla) followed by the chimpanzees (genus Pan). The splitting date between human and chimpanzee lineages is placed around 48 million years ago during the late Miocene epoch.[25][26] During this split, chromosome 2 was formed from two other chromosomes, leaving humans with only 23 pairs of chromosomes, compared to 24 for the other apes.[27][28]

There is little fossil evidence for the divergence of the gorilla, chimpanzee and hominin lineages.[29][30] The earliest fossils that have been proposed as members of the hominin lineage are Sahelanthropus tchadensis dating from 7 million years ago, Orrorin tugenensis dating from 5.7 million years ago, and Ardipithecus kadabba dating to 5.6 million years ago. Each of these species has been argued to be a bipedal ancestor of later hominins, but all such claims are contested. It is also possible that any one of the three is an ancestor of another branch of African apes, or is an ancestor shared between hominins and other African Hominoidea (apes). The question of the relation between these early fossil species and the hominin lineage is
still to be resolved. From these early species the australopithecines arose around 4 million years ago diverged into robust (also called Paranthropus) and gracile branches,[31] possibly one of which (such as A. garhi, dating to 2.5 million years ago) is a direct ancestor of the genus Homo.[32]

The earliest members of the genus Homo are Homo habilis which evolved around 2.8 million years ago.[33]Homo habilis has been considered the first species for which there is clear evidence of the use of stone tools. More recently, however, in 2015, stone tools, perhaps predating Homo habilis, have been discovered in northwestern Kenya that have been dated to 3.3 million years old.[34] Nonetheless, the brains of Homo habilis were about the same size as that of a chimpanzee, and their main adaptation was bipedalism as an adaptation to terrestrial living. During the next million years a process of encephalization began, and with the arrival of Homo erectus in the fossil record, cranial capacity had doubled. Homo erectus were the first of the hominina to leave Africa, and these species spread through Africa, Asia, and Europe between 1.3to1.8 million years ago. One population of H. erectus, also sometimes classified as a separate species Homo ergaster, stayed in Africa and evolved into Homo sapiens. It is believed that these species were the first to use fire and complex tools. The earliest transitional fossils between H. ergaster/erectus and archaic humans are from Africa such as Homo rhodesiensis, but seemingly transitional forms are also found at Dmanisi, Georgia. These descendants of African H. erectus spread through Eurasia from ca. 500,000 years ago evolving into H. antecessor, H. heidelbergensis and H. neanderthalensis. The earliest fossils of anatomically modern humans are from the Middle Paleolithic, about 200,000 years ago such as the Omo remains of Ethiopia and the fossils of Herto sometimes classified as Homo sapiens idaltu.[35] Later fossils of archaic Homo sapiens from Skhul in Israel and Southern Europe begin around 90,000 years ago.[36]

Human evolution is characterized by a number of morphological, developmental, physiological, and behavioral changes that have taken place since the split between the last common ancestor of humans and chimpanzees. The most significant of these adaptations are 1. bipedalism, 2. increased brain size, 3. lengthened ontogeny (gestation and infancy), 4. decreased sexual dimorphism (neoteny). The relationship between all these changes is the subject of ongoing debate.[37] Other significant morphological changes included the evolution of a power and precision grip, a change first occurring in H. erectus.[38]

Bipedalism is the basic adaption of the hominin line, and it is considered the main cause behind a suite of skeletal changes shared by all bipedal hominins. The earliest bipedal hominin is considered to be either Sahelanthropus[39] or Orrorin, with Ardipithecus, a full bipedal,[40] coming somewhat later.[citation needed] The knuckle walkers, the gorilla and chimpanzee, diverged around the same time, and either Sahelanthropus or Orrorin may be humans' last shared ancestor with those animals.[citation needed] The early bipedals eventually evolved into the australopithecines and later the genus Homo.[citation needed] There are several theories of the adaptational value of bipedalism. It is possible that bipedalism was favored because it freed up the hands for reaching and carrying food, because it saved energy during locomotion, because it enabled long distance running and hunting, or as a strategy for avoiding hyperthermia by reducing the surface exposed to direct sun.[citation needed]

The human species developed a much larger brain than that of other primates typically 1,330 cm3 in modern humans, over twice the size of that of a chimpanzee or gorilla.[41] The pattern of encephalization started with Homo habilis which at approximately 600cm3 had a brain slightly larger than chimpanzees, and continued with Homo erectus (8001100cm3), and reached a maximum in Neanderthals with an average size of 12001900cm3, larger even than Homo sapiens (but less encephalized).[42] The pattern of human postnatal brain growth differs from that of other apes (heterochrony), and allows for extended periods of social learning and language acquisition in juvenile humans. However, the differences between the structure of human brains and those of other apes may be even more significant than differences in size.[43][44][45][46] The increase in volume over time has affected different areas within the brain unequally the temporal lobes, which contain centers for language processing have increased disproportionately, as has the prefrontal cortex which has been related to complex decision making and moderating social behavior.[41] Encephalization has been tied to an increasing emphasis on meat in the diet,[47][48] or with the development of cooking,[49] and it has been proposed [50] that intelligence increased as a response to an increased necessity for solving social problems as human society became more complex.

The reduced degree of sexual dimorphism is primarily visible in the reduction of the male canine tooth relative to other ape species (except gibbons). Another important physiological change related to sexuality in humans was the evolution of hidden estrus. Humans are the only ape in which the female is fertile year round, and in which no special signals of fertility are produced by the body (such as genital swelling during estrus). Nonetheless humans retain a degree of sexual dimorphism in the distribution of body hair and subcutaneous fat, and in the overall size, males being around 25% larger than females. These changes taken together have been interpreted as a result of an increased emphasis on pair bonding as a possible solution to the requirement for increased parental investment due to the prolonged infancy of offspring.[citation needed]

By the beginning of the Upper Paleolithic period (50,000 BP), full behavioral modernity, including language, music and other cultural universals had developed.[51][52] As modern humans spread out from Africa they encountered other hominids such as Homo neanderthalensis and the so-called Denisovans. The nature of interaction between early humans and these sister species has been a long-standing source of controversy, the question being whether humans replaced these earlier species or whether they were in fact similar enough to interbreed, in which case these earlier populations may have contributed genetic material to modern humans.[53] Recent studies of the human and Neanderthal genomes suggest gene flow between archaic Homo sapiens and Neanderthals and Denisovans.[54][55][56] In March 2016, studies were published that suggest that modern humans bred with hominins, including Denisovans and Neanderthals, on multiple occasions.[57]

This dispersal out of Africa is estimated to have begun about 70,000 years BP from Northeast Africa. Current evidence suggests that there was only one such dispersal and that it only involved a few hundred individuals. The vast majority of humans stayed in Africa and adapted to a diverse array of environments.[58] Modern humans subsequently spread globally, replacing earlier hominins (either through competition or hybridization). They inhabited Eurasia and Oceania by 40,000 years BP, and the Americas at least 14,500 years BP.[59][60]

Until about 10,000 years ago, humans lived as hunter-gatherers. They gradually gained domination over much of the natural environment. They generally lived in small nomadic groups known as band societies, often in caves. The advent of agriculture prompted the Neolithic Revolution, when access to food surplus led to the formation of permanent human settlements, the domestication of animals and the use of metal tools for the first time in history. Agriculture encouraged trade and cooperation, and led to complex society.[citation needed]

The early civilizations of Mesopotamia, Egypt, India, China, Maya, Greece and Rome were some of the cradles of civilization.[61][6
2][63] The Late Middle Ages and the Early Modern Period saw the rise of revolutionary ideas and technologies. Over the next 500 years, exploration and European colonialism brought great parts of the world under European control, leading to later struggles for independence. The concept of the modern world as distinct from an ancient world is based on a rapid change progress in a brief period of time in many areas.[citation needed] Advances in all areas of human activity prompted new theories such as evolution and psychoanalysis, which changed humanity's views of itself.[citation needed] The Scientific Revolution, Technological Revolution and the Industrial Revolution up until the 19th century resulted in independent discoveries such as imaging technology, major innovations in transport, such as the airplane and automobile; energy development, such as coal and electricity.[64] This correlates with population growth (especially in America)[65] and higher life expectancy, the World population rapidly increased numerous times in the 19th and 20th centuries as nearly 10% of the 100 billion people lived in the past century.[66]

With the advent of the Information Age at the end of the 20th century, modern humans live in a world that has become increasingly globalized and interconnected. As of 2010, almost 2billion humans are able to communicate with each other via the Internet,[67] and 3.3 billion by mobile phone subscriptions.[68] Although interconnection between humans has encouraged the growth of science, art, discussion, and technology, it has also led to culture clashes and the development and use of weapons of mass destruction.[citation needed] Human civilization has led to environmental destruction and pollution significantly contributing to the ongoing mass extinction of other forms of life called the Holocene extinction event,[69] which may be further accelerated by global warming in the future.[70]

Early human settlements were dependent on proximity to water and, depending on the lifestyle, other natural resources used for subsistence, such as populations of animal prey for hunting and arable land for growing crops and grazing livestock. But humans have a great capacity for altering their habitats by means of technology, through irrigation, urban planning, construction, transport, manufacturing goods, deforestation and desertification. Deliberate habitat alteration is often done with the goals of increasing material wealth, increasing thermal comfort, improving the amount of food available, improving aesthetics, or improving ease of access to resources or other human settlements. With the advent of large-scale trade and transport infrastructure, proximity to these resources has become unnecessary, and in many places, these factors are no longer a driving force behind the growth and decline of a population. Nonetheless, the manner in which a habitat is altered is often a major determinant in population change.[citation needed]

Technology has allowed humans to colonize all of the continents and adapt to virtually all climates. Within the last century, humans have explored Antarctica, the ocean depths, and outer space, although large-scale colonization of these environments is not yet feasible. With a population of over seven billion, humans are among the most numerous of the large mammals. Most humans (61%) live in Asia. The remainder live in the Americas (14%), Africa (14%), Europe (11%), and Oceania (0.5%).[71]

Human habitation within closed ecological systems in hostile environments, such as Antarctica and outer space, is expensive, typically limited in duration, and restricted to scientific, military, or industrial expeditions. Life in space has been very sporadic, with no more than thirteen humans in space at any given time.[72] Between 1969 and 1972, two humans at a time spent brief intervals on the Moon. As of December 2016, no other celestial body has been visited by humans, although there has been a continuous human presence in space since the launch of the initial crew to inhabit the International Space Station on October 31, 2000.[73] However, other celestial bodies have been visited by human-made objects.[74][75][76]

Since 1800, the human population has increased from one billion[77] to over seven billion,[78] In 2004, some 2.5 billion out of 6.3 billion people (39.7%) lived in urban areas. In February 2008, the U.N. estimated that half the world's population would live in urban areas by the end of the year.[79] Problems for humans living in cities include various forms of pollution and crime,[80] especially in inner city and suburban slums. Both overall population numbers and the proportion residing in cities are expected to increase significantly in the coming decades.[81]

Humans have had a dramatic effect on the environment. Humans are apex predators, being rarely preyed upon by other species.[82] Currently, through land development, combustion of fossil fuels, and pollution, humans are thought to be the main contributor to global climate change.[83] If this continues at its current rate it is predicted that climate change will wipe out half of all plant and animal species over the next century.[84][85]

Most aspects of human physiology are closely homologous to corresponding aspects of animal physiology. The human body consists of the legs, the torso, the arms, the neck, and the head. An adult human body consists of about 100 trillion (1014) cells. The most commonly defined body systems in humans are the nervous, the cardiovascular, the circulatory, the digestive, the endocrine, the immune, the integumentary, the lymphatic, the muscoskeletal, the reproductive, the respiratory, and the urinary system.[86][87]

Humans, like most of the other apes, lack external tails, have several blood type systems, have opposable thumbs, and are sexually dimorphic. The comparatively minor anatomical differences between humans and chimpanzees are a result of human bipedalism. One difference is that humans have a far faster and more accurate throw than other animals. Humans are also among the best long-distance runners in the animal kingdom, but slower over short distances.[88][89] Humans' thinner body hair and more productive sweat glands help avoid heat exhaustion while running for long distances.[90]

As a consequence of bipedalism, human females have narrower birth canals. The construction of the human pelvis differs from other primates, as do the toes. A trade-off for these advantages of the modern human pelvis is that childbirth is more difficult and dangerous than in most mammals, especially given the larger head size of human babies compared to other primates. This means that human babies must turn around as they pass through the birth canal, which other primates do not do, and it makes humans the only species where females usually require help from their conspecifics (other members of their own species) to reduce the risks of birthing. As a partial evolutionary solution, human fetuses are born less developed and more vulnerable. Chimpanzee babies are cognitively more developed than human babies until the age of six months, when the rapid development of human brains surpasses chimpanzees. Another difference between women and chimpanzee females is that women go through the menopause and become unfertile decades before the end of their lives. All species of non-human apes are capable of giving birth until death. Menopause probably developed as it has provided an evolutionary advantage (more caring time) to young relatives.[89]

Apart from bipedalism, humans differ from chimpanzees mostly in smelling, hearing, digesting proteins, brain size, and the ability of language. Humans' brains are about three times bigger than in chimpanzees. More importantly, the brain to body ratio is much higher in humans than in chimpanzees, and humans have a significantly more developed cerebral cortex, with a larger number of neurons. The mental abilities of humans are remarkable compared to other apes. Humans' ability of speech is unique among primates. Humans are able to creat
e new and complex ideas, and to develop technology, which is unprecedented among other organisms on Earth.[89]

It is estimated that the worldwide average height for an adult human male is about 172cm (5ft 712in),[citation needed] while the worldwide average height for adult human females is about 158cm (5ft 2in).[citation needed] Shrinkage of stature may begin in middle age in some individuals, but tends to be typical in the extremely aged.[91] Through history human populations have universally become taller, probably as a consequence of better nutrition, healthcare, and living conditions.[92] The average mass of an adult human is 5464kg (120140lb) for females and 7683kg (168183lb) for males.[93] Like many other conditions, body weight and body type is influenced by both genetic susceptibility and environment and varies greatly among individuals. (see obesity)[94][95]

Although humans appear hairless compared to other primates, with notable hair growth occurring chiefly on the top of the head, underarms and pubic area, the average human has more hair follicles on his or her body than the average chimpanzee. The main distinction is that human hairs are shorter, finer, and less heavily pigmented than the average chimpanzee's, thus making them harder to see.[96] Humans have about 2 million sweat glands spread over their entire bodies, many more than chimpanzees, whose sweat glands are scarce and are mainly located on the palm of the hand and on the soles of the feet.[97]

The dental formula of humans is: 2.1.2.32.1.2.3. Humans have proportionately shorter palates and much smaller teeth than other primates. They are the only primates to have short, relatively flush canine teeth. Humans have characteristically crowded teeth, with gaps from lost teeth usually closing up quickly in young individuals. Humans are gradually losing their wisdom teeth, with some individuals having them congenitally absent.[98]

Like all mammals, humans are a diploid eukaryotic species. Each somatic cell has two sets of 23 chromosomes, each set received from one parent; gametes have only one set of chromosomes, which is a mixture of the two parental sets. Among the 23 pairs of chromosomes there are 22 pairs of autosomes and one pair of sex chromosomes. Like other mammals, humans have an XY sex-determination system, so that females have the sex chromosomes XX and males have XY.[99]

One human genome was sequenced in full in 2003, and currently efforts are being made to achieve a sample of the genetic diversity of the species (see International HapMap Project). By present estimates, humans have approximately 22,000 genes.[100] The variation in human DNA is very small compared to other species, possibly suggesting a population bottleneck during the Late Pleistocene (around 100,000 years ago), in which the human population was reduced to a small number of breeding pairs.[101][102]Nucleotide diversity is based on single mutations called single nucleotide polymorphisms (SNPs). The nucleotide diversity between humans is about 0.1%, i.e. 1 difference per 1,000 base pairs.[103][104] A difference of 1 in 1,000 nucleotides between two humans chosen at random amounts to about 3 million nucleotide differences, since the human genome has about 3 billion nucleotides. Most of these single nucleotide polymorphisms (SNPs) are neutral but some (about 3 to 5%) are functional and influence phenotypic differences between humans through alleles.[citation needed]

By comparing the parts of the genome that are not under natural selection and which therefore accumulate mutations at a fairly steady rate, it is possible to reconstruct a genetic tree incorporating the entire human species since the last shared ancestor. Each time a certain mutation (SNP) appears in an individual and is passed on to his or her descendants, a haplogroup is formed including all of the descendants of the individual who will also carry that mutation. By comparing mitochondrial DNA, which is inherited only from the mother, geneticists have concluded that the last female common ancestor whose genetic marker is found in all modern humans, the so-called mitochondrial Eve, must have lived around 90,000 to 200,000 years ago.[105][106][107]

Human accelerated regions, first described in August 2006,[108][109] are a set of 49 segments of the human genome that are conserved throughout vertebrate evolution but are strikingly different in humans. They are named according to their degree of difference between humans and their nearest animal relative (chimpanzees) (HAR1 showing the largest degree of human-chimpanzee differences). Found by scanning through genomic databases of multiple species, some of these highly mutated areas may contribute to human-specific traits.[citation needed]

The forces of natural selection have continued to operate on human populations, with evidence that certain regions of the genome display directional selection in the past 15,000 years.[110]

As with other mammals, human reproduction takes place as internal fertilization by sexual intercourse. During this process, the male inserts his erect penis into the female's vagina and ejaculates semen, which contains sperm. The sperm travels through the vagina and cervix into the uterus or Fallopian tubes for fertilization of the ovum. Upon fertilization and implantation, gestation then occurs within the female's uterus.

The zygote divides inside the female's uterus to become an embryo, which over a period of 38 weeks (9 months) of gestation becomes a fetus. After this span of time, the fully grown fetus is birthed from the woman's body and breathes independently as an infant for the first time. At this point, most modern cultures recognize the baby as a person entitled to the full protection of the law, though some jurisdictions extend various levels of personhood earlier to human fetuses while they remain in the uterus.

Compared with other species, human childbirth is dangerous. Painful labors lasting 24 hours or more are not uncommon and sometimes lead to the death of the mother, the child or both.[111] This is because of both the relatively large fetal head circumference and the mother's relatively narrow pelvis.[112][113] The chances of a successful labor increased significantly during the 20th century in wealthier countries with the advent of new medical technologies. In contrast, pregnancy and natural childbirth remain hazardous ordeals in developing regions of the world, with maternal death rates approximately 100 times greater than in developed countries.[114]

In developed countries, infants are typically 34kg (69pounds) in weight and 5060cm (2024inches) in height at birth.[115][not in citation given] However, low birth weight is common in developing countries, and contributes to the high levels of infant mortality in these regions.[116] Helpless at birth, humans continue to grow for some years, typically reaching sexual maturity at 12 to 15years of age. Females continue to develop physically until around the age of 18, whereas male development continues until around age 21. The human life span can be split into a number of stages: infancy, childhood, adolescence, young adulthood, adulthood and old age. The lengths of these stages, however, have varied across cultures and time periods. Compared to other primates, humans experience an unusually rapid growth spurt during adolescence, where the body grows 25% in size. Chimpanzees, for example, grow only 14%, with no pronounced spurt.[117] The presence of the growth spurt is probably necessary to keep children physically small until they are psychologically mature. Humans are one of the few species in which females undergo menopause. It has been proposed that menopause increases a woman's overall reproductive success by allowing her to invest more time and resources in her existing offspring, and in turn their children (the grandmother hypothesis), rather than by continuing to bear children into old age.[118][119]

For various reasons, including biological/genetic causes,[120] women live on average about four
years longer than menas of 2013 the global average life expectancy at birth of a girl is estimated at 70.2 years compared to 66.1 for a boy.[121] There are significant geographical variations in human life expectancy, mostly correlated with economic developmentfor example life expectancy at birth in Hong Kong is 84.8years for girls and 78.9 for boys, while in Swaziland, primarily because of AIDS, it is 31.3years for both sexes.[122] The developed world is generally aging, with the median age around 40years. In the developing world the median age is between 15 and 20years. While one in five Europeans is 60years of age or older, only one in twenty Africans is 60years of age or older.[123] The number of centenarians (humans of age 100years or older) in the world was estimated by the United Nations at 210,000 in 2002.[124] At least one person, Jeanne Calment, is known to have reached the age of 122years;[125] higher ages have been claimed but they are not well substantiated.

Humans are omnivorous, capable of consuming a wide variety of plant and animal material.[126][127] Varying with available food sources in regions of habitation, and also varying with cultural and religious norms, human groups have adopted a range of diets, from purely vegetarian to primarily carnivorous. In some cases, dietary restrictions in humans can lead to deficiency diseases; however, stable human groups have adapted to many dietary patterns through both genetic specialization and cultural conventions to use nutritionally balanced food sources.[128] The human diet is prominently reflected in human culture, and has led to the development of food science.

Until the development of agriculture approximately 10,000 years ago, Homo sapiens employed a hunter-gatherer method as their sole means of food collection. This involved combining stationary food sources (such as fruits, grains, tubers, and mushrooms, insect larvae and aquatic mollusks) with wild game, which must be hunted and killed in order to be consumed.[129] It has been proposed that humans have used fire to prepare and cook food since the time of Homo erectus.[130] Around ten thousand years ago, humans developed agriculture,[131] which substantially altered their diet. This change in diet may also have altered human biology; with the spread of dairy farming providing a new and rich source of food, leading to the evolution of the ability to digest lactose in some adults.[132][133] Agriculture led to increased populations, the development of cities, and because of increased population density, the wider spread of infectious diseases. The types of food consumed, and the way in which they are prepared, have varied widely by time, location, and culture.

In general, humans can survive for two to eight weeks without food, depending on stored body fat. Survival without water is usually limited to three or four days. About 36 million humans die every year from causes directly or indirectly related to starvation.[134] Childhood malnutrition is also common and contributes to the global burden of disease.[135] However global food distribution is not even, and obesity among some human populations has increased rapidly, leading to health complications and increased mortality in some developed, and a few developing countries. Worldwide over one billion people are obese,[136] while in the United States 35% of people are obese, leading to this being described as an "obesity epidemic."[137] Obesity is caused by consuming more calories than are expended, so excessive weight gain is usually caused by an energy-dense diet.[136]

No two humansnot even monozygotic twinsare genetically identical. Genes and environment influence human biological variation from visible characteristics to physiology to disease susceptibly to mental abilities. The exact influence of genes and environment on certain traits is not well understood.[138][139]

Most current genetic and archaeological evidence supports a recent single origin of modern humans in East Africa,[140] with first migrations placed at 60,000 years ago. Compared to the great apes, human gene sequenceseven among African populationsare remarkably homogeneous.[141] On average, genetic similarity between any two humans is 99.9%.[142][143] There is about 23 times more genetic diversity within the wild chimpanzee population, than in the entire human gene pool.[144][145][146]

The human body's ability to adapt to different environmental stresses is remarkable, allowing humans to acclimatize to a wide variety of temperatures, humidity, and altitudes. As a result, humans are a cosmopolitan species found in almost all regions of the world, including tropical rainforests, arid desert, extremely cold arctic regions, and heavily polluted cities. Most other species are confined to a few geographical areas by their limited adaptability.[147]

There is biological variation in the human specieswith traits such as blood type, cranial features, eye color, hair color and type, height and build, and skin color varying across the globe. Human body types vary substantially. The typical height of an adult human is between 1.4m and 1.9m (4ft 7 in and 6ft 3 in), although this varies significantly depending, among other things, on sex and ethnic origin.[148][149] Body size is partly determined by genes and is also significantly influenced by environmental factors such as diet, exercise, and sleep patterns, especially as an influence in childhood. Adult height for each sex in a particular ethnic group approximately follows a normal distribution. Those aspects of genetic variation that give clues to human evolutionary history, or are relevant to medical research, have received particular attention. For example, the genes that allow adult humans to digest lactose are present in high frequencies in populations that have long histories of cattle domestication, suggesting natural selection having favored that gene in populations that depend on cow milk. Some hereditary diseases such as sickle cell anemia are frequent in populations where malaria has been endemic throughout historyit is believed that the same gene gives increased resistance to malaria among those who are unaffected carriers of the gene. Similarly, populations that have for a long time inhabited specific climates, such as arctic or tropical regions or high altitudes, tend to have developed specific phenotypes that are beneficial for conserving energy in those environmentsshort stature and stocky build in cold regions, tall and lanky in hot regions, and with high lung capacities at high altitudes. Similarly, skin color varies clinally with darker skin around the equatorwhere the added protection from the sun's ultraviolet radiation is thought to give an evolutionary advantageand lighter skin tones closer to the poles.[150][151][152][153]

The hue of human skin and hair is determined by the presence of pigments called melanins. Human skin color can range from darkest brown to lightest peach, or even nearly white or colorless in cases of albinism.[146] Human hair ranges in color from white to red to blond to brown to black, which is most frequent.[154] Hair color depends on the amount of melanin (an effective sun blocking pigment) in the skin and hair, with hair melanin concentrations in hair fading with increased age, leading to grey or even white hair. Most researchers believe that skin darkening is an adaptation that evolved as protection against ultraviolet solar radiation, which also helps balancing folate, which is destroyed by ultraviolet radiation. Light skin pigmentation protects against depletion of vitamin D, which requires sunlight to make.[155] Skin pigmentation of contemporary humans is clinally distributed across the planet, and in general correlates with the level of ultraviolet radiation in a particular geographic area. Human skin also has a capacity to darken (tan) in response to exposure to ultraviolet radiation.[156][157][158]

Within the human species, the greatest degree of genetic variation exists between males and females. While the nucleotide genetic variation of
individuals of the same sex across global populations is no greater than 0.1%, the genetic difference between males and females is between 1% and 2%. Although different in nature[clarification needed], this approaches the genetic differentiation between men and male chimpanzees or women and female chimpanzees. The genetic difference between sexes contributes to anatomical, hormonal, neural, and physiological differences between men and women, although the exact degree and nature of social and environmental influences on sexes are not completely understood. Males on average are 15% heavier and 15cm taller than females. There is a difference between body types, body organs and systems, hormonal levels, sensory systems, and muscle mass between sexes. On average, there is a difference of about 4050% in upper body strength and 2030% in lower body strength between men and women. Women generally have a higher body fat percentage than men. Women have lighter skin than men of the same population; this has been explained by a higher need for vitamin D (which is synthesized by sunlight) in females during pregnancy and lactation. As there are chromosomal differences between females and males, some X and Y chromosome related conditions and disorders only affect either men or women. Other conditional differences between males and females are not related to sex chromosomes. Even after allowing for body weight and volume, the male voice is usually an octave deeper than the female voice. Women have a longer life span in almost every population around the world.[160][161][162][163][164][165][166][167][168]

Males typically have larger tracheae and branching bronchi, with about 30% greater lung volume per unit body mass. They have larger hearts, 10% higher red blood cell count, and higher hemoglobin, hence greater oxygen-carrying capacity. They also have higher circulating clotting factors (vitamin K, prothrombin and platelets). These differences lead to faster healing of wounds and higher peripheral pain tolerance.[169] Females typically have more white blood cells (stored and circulating), more granulocytes and B and T lymphocytes. Additionally, they produce more antibodies at a faster rate than males. Hence they develop fewer infectious diseases and these continue for shorter periods.[169]Ethologists argue that females, interacting with other females and multiple offspring in social groups, have experienced such traits as a selective advantage.[170][171][172][173][174] According to Daly and Wilson, "The sexes differ more in human beings than in monogamous mammals, but much less than in extremely polygamous mammals."[175] But given that sexual dimorphism in the closest relatives of humans is much greater than among humans, the human clade must be considered to be characterized by decreasing sexual dimorphism, probably due to less competitive mating patterns. One proposed explanation is that human sexuality has developed more in common with its close relative the bonobo, which exhibits similar sexual dimorphism, is polygynandrous and uses recreational sex to reinforce social bonds and reduce aggression.[176]

Humans of the same sex are 99.9% genetically identical. There is extremely little variation between human geographical populations, and most of the variation that does occur is at the personal level within local areas, and not between populations.[146][177][178] Of the 0.1% of human genetic differentiation, 85% exists within any randomly chosen local population, be they Italians, Koreans, or Kurds. Two randomly chosen Koreans may be genetically as different as a Korean and an Italian. Any ethnic group contains 85% of the human genetic diversity of the world. Genetic data shows that no matter how population groups are defined, two people from the same population group are about as different from each other as two people from any two different population groups.[146][179][180][181]

Current genetic research has demonstrated that humans on the African continent are the most genetically diverse.[182] There is more human genetic diversity in Africa than anywhere else on Earth. The genetic structure of Africans was traced to 14 ancestral population clusters. Human genetic diversity decreases in native populations with migratory distance from Africa and this is thought to be the result of bottlenecks during human migration.[183][184] Humans have lived in Africa for the longest time, which has allowed accumulation of a higher diversity of genetic mutations in these populations. Only part of Africa's population migrated out of the continent, bringing just part of the original African genetic variety with them. African populations harbor genetic alleles that are not found in other places of the world. All the common alleles found in populations outside of Africa are found on the African continent.[146]

Geographical distribution of human variation is complex and constantly shifts through time which reflects complicated human evolutionary history. Most human biological variation is clinally distributed and blends gradually from one area to the next. Groups of people around the world have different frequencies of polymorphic genes. Furthermore, different traits are non-concordant and each have different clinal distribution. Adaptability varies both from person to person and from population to population. The most efficient adaptive responses are found in geographical populations where the environmental stimuli are the strongest (e.g. Tibetans are highly adapted to high altitudes). The clinal geographic genetic variation is further complicated by the migration and mixing between human populations which has been occurring since prehistoric times.[146][185][186][187][188][189]

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Genetic Engineering: The Past, Present, and Future – The …

Inside this Article

This most pleasant, easy to read, and informative article takes you on an even easier to follow journey from a basic definition of genetic engineering through a couple of interesting historical highlights, then quickly moves you from an understanding of how genetic engineering is done, to its applications in the real world now and in the future. In closing Dr. Hadzimichalis provides a few thoughtful remarks on todays ethical and regulatory considerations.

In humans, as with any other organism, genetic engineering refers to any changes in genetic makeup that result from the direct manipulation of DNA using various technical methods. While this term is used often in mainstream media, much of the general population does not have a clear understanding of its meaning, current uses, and potential applications. The process of genetic engineering is intended to produce a useful or desirable characteristic in an organism and on a molecular level and may include additions, deletions, or targeted changes to the genome. More simply put, genetic engineering involves cutting, pasting, and/or editing DNA to produce a valuable effect. Interestingly, these alterations can involve introduction of genetic material from either the same or from different type of organism.

A variety of methods may be employed to produce a genetically modified organism (GMO). Historically, and still today, humans have indirectly modified the genomes of other species to produce desired products including domesticated animals and high yield plants varieties. By selecting the seeds from the best produce for next years crop and using the hardiest steers to fertilize the herd, food staples became gradually more robust and abundant.

However, breakthrough experiments from Hersey and Chase in 1952 confirming that DNA is the vessel for our genetic code, initiated further characterization of this biological macromolecule and prompted an in depth examination into methods to specifically modify it (http://jgp.rupress.org/content/36/1/39.full.pdf)). This has decreased the time it takes to appreciably improve an organism from decades and even centuries down to weeks and months.

Dr. Paul Berg and colleagues are credited with creating the first ever recombinant DNA molecule (molecules that are DNA sequences resulting from the use of laboratory methods), published in 1972. In this study, they described a novel way to combine DNA from different organisms and in fact, successfully combined DNA from a monkey virus (SV40) and a bacterial virus (lambda phage) (http://www.ncbi.nlm.nih.gov/pmc/articles/PMC389671/). For this work, Dr. Berg was awarded the 1980 Nobel Prize in chemistry for his fundamental studies of the biochemistry of nucleic acids, with particular regard to recombinant-DNA (http://www.nobelprize.org/nobel_prizes/chemistry/laureates/1980/).

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Genetic Engineering: The Past, Present, and Future - The ...

Human Genetic Enhancements: A Transhumanist Perspective

1. What is Transhumanism?

Transhumanism is a loosely defined movement that has developed gradually over the past two decades. It promotes an interdisciplinary approach to understanding and evaluating the opportunities for enhancing the human condition and the human organism opened up by the advancement of technology. Attention is given to both present technologies, like genetic engineering and information technology, and anticipated future ones, such as molecular nanotechnology and artificial intelligence.1

The enhancement options being discussed include radical extension of human health-span, eradication of disease, elimination of unnecessary suffering, and augmentation of human intellectual, physical, and emotional capacities.2 Other transhumanist themes include space colonization and the possibility of creating superintelligent machines, along with other potential developments that could profoundly alter the human condition. The ambit is not limited to gadgets and medicine, but encompasses also economic, social, institutional designs, cultural development, and psychological skills and techniques.

Transhumanists view human nature as a work-in-progress, a half-baked beginning that we can learn to remold in desirable ways. Current humanity need not be the endpoint of evolution. Transhumanists hope that by responsible use of science, technology, and other rational means we shall eventually manage to become post-human, beings with vastly greater capacities than present human beings have.

Some transhumanists take active steps to increase the probability that they personally will survive long enough to become post-human, for example by choosing a healthy lifestyle or by making provisions for having themselves cryonically suspended in case of de-animation.3 In contrast to many other ethical outlooks, which in practice often reflect a reactionary attitude to new technologies, the transhumanist view is guided by an evolving vision to take a more active approach to technology policy. This vision, in broad strokes, is to create the opportunity to live much longer and healthier lives, to enhance our memory and other intellectual faculties, to refine our emotional experiences and increase our subjective sense of well-being, and generally to achieve a greater degree of control over our own lives. This affirmation of human potential is offered as an alternative to customary injunctions against playing God, messing with nature, tampering with our human essence, or displaying punishable hubris.

Transhumanism does not entail technological optimism. While future technological capabilities carry immense potential for beneficial deployments, they also could be misused to cause enormous harm, ranging all the way to the extreme possibility of intelligent life becoming extinct. Other potential negative outcomes include widening social inequalities or a gradual erosion of the hard-to-quantify assets that we care deeply about but tend to neglect in our daily struggle for material gain, such as meaningful human relationships and ecological diversity. Such risks must be taken very seriously, as thoughtful transhumanists fully acknowledge.4

Transhumanism has roots in secular humanist thinking, yet is more radical in that it promotes not only traditional means of improving human nature, such as education and cultural refinement, but also direct application of medicine and technology to overcome some of our basic biological limits.

2. A Core Transhumanist Value: Exploring the Post-human Realm

The range of thoughts, feelings, experiences, and activities that are accessible to human organisms presumably constitute only a tiny part of what is possible. There is no reason to think that the human mode of being is any more free of limitations imposed by our biological nature than are the modes of being of other animals. Just as chimpanzees lack the brainpower to understand what it is like to be human, so too do we lack the practical ability to form a realistic intuitive understanding of what it would be like to be post-human.

This point is distinct from any principled claims about impossibility. We need not assert that post-humans would not be Turing computable or that their concepts could not be expressed by any finite sentences in human language. The impossibility is more like the impossibility for us to visualize a twenty-dimensional hypersphere or to read, with perfect recollection and understanding, every book in the Library of Congress. Our own current mode of being, therefore, spans but a minute subspace of what is possible or permitted by the physical constraints of the universe. It is not farfetched to suppose that there are parts of this larger space that represent extremely valuable ways of living, feeling, and thinking.

We can conceive of aesthetic and contemplative pleasures whose blissfulness vastly exceeds what any human being has yet experienced. We can imagine beings that reach a much greater level of personal development and maturity than current human beings do, because they have the opportunity to live for hundreds or thousands of years with full bodily and psychic vigor. We can conceive of beings that are much smarter than us, that can read books in seconds, that are much more brilliant philosophers than we are, that can create artworks, which, even if we could understand them only on the most superficial level, would strike us as wonderful masterpieces. We can imagine love that is stronger, purer, and more secure than any human being has yet harbored. Our everyday intuitions about values are constrained by the narrowness of our experience and the limitations of our powers of imagination. We should leave room in our thinking for the possibility that as we develop greater capacities, we shall come to discover values that will strike us as being of a far higher order than those we can realize as un-enhanced biological humans beings.

The conjecture that there are greater values than we can currently fathom does not imply that values are not defined in terms of our current dispositions. Take, for example, a dispositional theory of value such as the one described by David Lewis.5 According to Lewiss theory, something is a value for you if and only if you would want to want it if you were perfectly acquainted with it and you were thinking and deliberating as clearly as possible about it. On this view, there may be values that we do not currently want, and that we do not even currently want to want, because we may not be perfectly acquainted with them or because we are not ideal deliberators. Some values pertaining to certain forms of post-human existence may well be of this sort; they may be values for us now, and they may be so in virtue of our current dispositions, and yet we may not be able to fully appreciate them with our current limited deliberative capacities and our lack of the receptive faculties required for full acquaintance with them. This point is important because it shows that the transhumanist view that we ought to explore the realm of post-human values does not entail that we should forego our current values. The post-human values can be our current values, albeit ones that we have not yet clearly comprehended. Transhumanism does not require us to say that we should favor post-human beings over human beings, but that the right way of favoring human beings is by enabling us to realize our ideals better and that some of our ideals may well be located outside the space of modes of being that are accessible to us with our current biological constitution.

We can overcome many of our biological limitations. It is possible that there are some limitations that are impossible for us to transcend, not only because of technological difficulties but on metaphysical grounds. Depending on what our views are about what constitutes personal identity, it could be that certain modes of being, while possible, are not possible for us, because any being of such a kind would be so different from us that they could not be us. Concer
ns of this kind are familiar from theological discussions of the afterlife. In Christian theology, some souls will be allowed by God to go to heaven after their time as corporal creatures is over. Before being admitted to heaven, the souls would undergo a purification process in which they would lose many of their previous bodily attributes. Skeptics may doubt that the resulting minds would be sufficiently similar to our current minds for it to be possible for them to be the same person. A similar predicament arises within transhumanism: if the mode of being of a post-human being is radically different from that of a human being, then we may doubt whether a post-human being could be the same person as a human being, even if the post-human being originated from a human being.

We can, however, envision many enhancements that would not make it impossible for the post-transformation someone to be the same person as the pre-transformation person. A person could obtain considerable increased life expectancy, intelligence, health, memory, and emotional sensitivity, without ceasing to exist in the process. A persons intellectual life can be transformed radically by getting an education. A persons life expectancy can be extended substantially by being unexpectedly cured from a lethal disease. Yet these developments are not viewed as spelling the end of the original person. In particular, it seems that modifications that add to a persons capacities can be more substantial than modifications that subtract, such as brain damage. If most of someone currently is, including her most important memories, activities, and feelings, is preserved, then adding extra capacities on top of that would not easily cause the person to cease to exist.

Preservation of personal identity, especially if this notion is given a narrow construal, is not everything. We can value other things than ourselves, or we might regard it as satisfactory if some parts or aspects of ourselves survive and flourish, even if that entails giving up some parts of ourselves such that we no longer count as being the same person. Which parts of ourselves we might be willing to sacrifice may not become clear until we are more fully acquainted with the full meaning of the options. A careful, incremental exploration of the post-human realm may be indispensable for acquiring such an understanding, although we may also be able to learn from each others experiences and from works of the imagination. Additionally, we may favor future people being posthuman rather than human, if the posthumans would lead lives more worthwhile than the alternative humans would. Any reasons stemming from such considerations would not depend on the assumption that we ourselves could become posthuman beings.

Transhumanism promotes the quest to develop further so that we can explore hitherto inaccessible realms of value. Technological enhancement of human organisms is a means that we ought to pursue to this end. There are limits to how much can be achieved by low-tech means such as education, philosophical contemplation, moral self-scrutiny and other such methods proposed by classical philosophers with perfectionist leanings, including Plato, Aristotle, and Nietzsche, or by means of creating a fairer and better society, as envisioned by social reformists such as Marx or Martin Luther King. This is not to denigrate what we can do with the tools we have today. Yet ultimately, transhumanists hope to go further.

3. The Morality of Human Germ-Line Genetic Engineering

Most potential human enhancement technologies have so far received scant attention in the ethics literature. One exception is genetic engineering, the morality of which has been extensively debated in recent years. To illustrate how the transhumanist approach can be applied to particular technologies, we shall therefore now turn to consider the case of human germ-line genetic enhancements.

Certain types of objection against germ-line modifications are not accorded much weight by a transhumanist interlocutor. For instance, objections that are based on the idea that there is something inherently wrong or morally suspect in using science to manipulate human nature are regarded by transhumanists as wrongheaded. Moreover, transhumanists emphasize that particular concerns about negative aspects of genetic enhancements, even when such concerns are legitimate, must be judged against the potentially enormous benefits that could come from genetic technology successfully employed.6 For example, many commentators worry about the psychological effects of the use of germ-line engineering. The ability to select the genes of our children and to create so-called designer babies will, it is claimed, corrupt parents, who will come to view their children as mere products.7 We will then begin to evaluate our offspring according to standards of quality control, and this will undermine the ethical ideal of unconditional acceptance of children, no matter what their abilities and traits. Are we really prepared to sacrifice on the altar of consumerism even those deep values that are embodied in traditional relationships between child and parents? Is the quest for perfection worth this cultural and moral cost? A transhumanist should not dismiss such concerns as irrelevant. Transhumanists recognize that the depicted outcome would be bad. We do not want parents to love and respect their children less. We do not want social prejudice against people with disabilities to get worse. The psychological and cultural effects of commodifying human nature are potentially important.

But such dystopian scenarios are speculations. There is no firm ground for believing that the alleged consequences would actually happen. What relevant evidence we have, for instance regarding the treatment of children who have been conceived through the use of in vitro fertilization or embryo screening, suggests that the pessimistic prognosis is alarmist. Parents will in fact love and respect their children even when artificial means and conscious choice play a part in procreation.

We might speculate, instead, that germ-line enhancements will lead to more love and parental dedication. Some mothers and fathers might find it easier to love a child who, thanks to enhancements, is bright, beautiful, healthy, and happy. The practice of germ-line enhancement might lead to better treatment of people with disabilities, because a general demystification of the genetic contributions to human traits could make it clearer that people with disabilities are not to blame for their disabilities and a decreased incidence of some disabilities could lead to more assistance being available for the remaining affected people to enable them to live full, unrestricted lives through various technological and social supports. Speculating about possible psychological or cultural effects of germ-line engineering can therefore cut both ways. Good consequences no less than bad ones are possible. In the absence of sound arguments for the view that the negative consequences would predominate, such speculations provide no reason against moving forward with the technology.

Ruminations over hypothetical side-effects may serve to make us aware of things that could go wrong so that we can be on the lookout for untoward developments. By being aware of the perils in advance, we will be in a better position to take preventive countermeasures. For instance, if we think that some people would fail to realize that a human clone would be a unique person deserving just as much respect and dignity as any other human being, we could work harder to educate the public on the inadequacy of genetic determinism. The theoretical contributions of well-informed and reasonable critics of germ-line enhancement could indirectly add to our justification for proceeding with germ-line engineering. To the extent that the critics have done their job, they can alert us to many of the potential untoward consequences of germ-line engineering and contribute to our ability to take precautions, thus improving the odds t
hat the balance of effects will be positive. There may well be some negative consequences of human germ-line engineering that we will not forestall, though of course the mere existence of negative effects is not a decisive reason not to proceed. Every major technology has some negative consequences. Only after a fair comparison of the risks with the likely positive consequences can any conclusion based on a cost-benefit analysis be reached.

In the case of germ-line enhancements, the potential gains are enormous. Only rarely, however, are the potential gains discussed, perhaps because they are too obvious to be of much theoretical interest. By contrast, uncovering subtle and non-trivial ways in which manipulating our genome could undermine deep values is philosophically a lot more challenging. But if we think about it, we recognize that the promise of genetic enhancements is anything but insignificant. Being free from severe genetic diseases would be good, as would having a mind that can learn more quickly, or having a more robust immune system. Healthier, wittier, happier people may be able to reach new levels culturally. To achieve a significant enhancement of human capacities would be to embark on the transhuman journey of exploration of some of the modes of being that are not accessible to us as we are currently constituted, possibly to discover and to instantiate important new values. On an even more basic level, genetic engineering holds great potential for alleviating unnecessary human suffering. Every day that the introduction of effective human genetic enhancement is delayed is a day of lost individual and cultural potential, and a day of torment for many unfortunate sufferers of diseases that could have been prevented. Seen in this light, proponents of a ban or a moratorium on human genetic modification must take on a heavy burden of proof in order to have the balance of reason tilt in their favor. Transhumanists conclude that the challenge has not been met.

4. Should Human Reproduction be Regulated?

One way of going forward with genetic engineering is to permit everything, leaving all choices to parents. While this attitude may be consistent with transhumanism, it is not the best transhumanist approach. One thing that can be said for adopting a libertarian stance in regard to human reproduction is the sorry track record of socially planned attempts to improve the human gene pool. The list of historical examples of state intervention in this domain ranges from the genocidal horrors of the Nazi regime, to the incomparably milder but still disgraceful semi-coercive sterilization programs of mentally impaired individuals favored by many well-meaning socialists in the past century, to the controversial but perhaps understandable program of the current Chinese government to limit population growth. In each case, state policies interfered with the reproductive choices of individuals. If parents had been left to make the choices for themselves, the worst transgressions of the eugenics movement would not have occurred. Bearing this in mind, we ought to think twice before giving our support to any proposal that would have the state regulate what sort of children people are allowed to have and the methods that may be used to conceive them.8

We currently permit governments to have a role in reproduction and child-rearing and we may reason by extension that there would likewise be a role in regulating the application of genetic reproductive technology. State agencies and regulators play a supportive and supervisory role, attempting to promote the interests of the child. Courts intervene in cases of child abuse or neglect. Some social policies are in place to support children from disadvantaged backgrounds and to ameliorate some of the worst inequities suffered by children from poor homes, such as through the provision of free schooling. These measures have analogues that apply to genetic enhancement technologies. For example, we ought to outlaw genetic modifications that are intended to damage the child or limit its opportunities in life, or that are judged to be too risky. If there are basic enhancements that would be beneficial for a child but that some parents cannot afford, then we should consider subsidizing those enhancements, just as we do with basic education. There are grounds for thinking that the libertarian approach is less appropriate in the realm of reproduction than it is in other areas. In reproduction, the most important interests at stake are those of the child-to-be, who cannot give his or her advance consent or freely enter into any form of contract. As it is, we currently approve of many measures that limit parental freedoms. We have laws against child abuse and child neglect. We have obligatory schooling. In some cases, we can force needed medical treatment on a child, even against the wishes of its parents.

There is a difference between these social interventions with regard to children and interventions aimed at genetic enhancements. While there is a consensus that nobody should be subjected to child abuse and that all children should have at least a basic education and should receive necessary medical care, it is unlikely that we will reach an agreement on proposals for genetic enhancements any time soon. Many parents will resist such proposals on principled grounds, including deep-seated religious or moral convictions. The best policy for the foreseeable future may therefore be to not legally require any genetic enhancements, except perhaps in extreme cases for which there is no alternative treatment. Even in such cases, it is dubious that the social climate in many countries is ready for mandatory genetic interventions.

The scope for ethics and public policy, however, extend far beyond the passing of laws requiring or banning specific interventions. Even if a given enhancement option is neither outlawed nor legally required, we may still seek to discourage or encourage its use in a variety of ways. Through subsidies and taxes, research-funding policies, genetic counseling practices and guidelines, laws regulating genetic information and genetic discrimination, provision of health care services, regulation of the insurance industry, patent law, education, and through the allocation of social approbation and disapproval, we may influence the direction in which particular technologies are applied. We may appropriately ask, with regard to genetic enhancement technologies, which types of applications we ought to promote or discourage.

5. Which Modifications Should Be Promoted and which Discouraged?

An externality, as understood by economists, is a cost or a benefit of an action that is not carried by a decision-maker. An example of a negative externality might be found in a firm that lowers its production costs by polluting the environment. The firm enjoys most of the benefits while escaping the costs, such as environmental degradation, which may instead paid by people living nearby. Externalities can also be positive, as when people put time and effort into creating a beautiful garden outside their house. The effects are enjoyed not exclusively by the gardeners but spill over to passersby. As a rule of thumb, sound social policy and social norms would have us internalize many externalities so that the incentives of producers more closely match the social value of production. We may levy a pollution tax on the polluting firm, for instance, and give our praise to the home gardeners who beautify the neighborhood.

Genetic enhancements aimed at the obtainment of goods that are desirable only in so far as they provide a competitive advantage tend to have negative externalities. An example of such a positional good, as economists call them, is stature. There is evidence that being tall is statistically advantageous, at least for men in Western societies. Taller men earn more money, wield greater social influence, and are viewed as more sexually attractive. Parents wanting to give their child the best possible start in life may rationally choose a genet
ic enhancement that adds an inch or two to the expected length of their offspring. Yet for society as a whole, there seems to be no advantage whatsoever in people being taller. If everybody grew two inches, nobody would be better off than they were before. Money spent on a positional good like length has little or no net effect on social welfare and is therefore, from societys point of view, wasted.

Health is a very different type of good. It has intrinsic benefits. If we become healthier, we are personally better off and others are not any worse off. There may even be a positive externality of enhancing ours own health. If we are less likely to contract a contagious disease, others benefit by being less likely to get infected by us. Being healthier, you may also contribute more to society and consume less of publicly funded healthcare.

If we were living in a simple world where people were perfectly rational self-interested economic agents and where social policies had no costs or unintended effects, then the basic policy prescription regarding genetic enhancements would be relatively straightforward. We should internalize the externalities of genetic enhancements by taxing enhancements that have negative externalities and subsidizing enhancements that have positive externalities. Unfortunately, crafting policies that work well in practice is considerably more difficult. Even determining the net size of the externalities of a particular genetic enhancement can be difficult. There is clearly an intrinsic value to enhancing memory or intelligence in as much as most of us would like to be a bit smarter, even if that did not have the slightest effect on our standing in relation to others. But there would also be important externalities, both positive and negative. On the negative side, others would suffer some disadvantage from our increased brainpower in that their own competitive situation would be worsened. Being more intelligent, we would be more likely to attain high-status positions in society, positions that would otherwise have been enjoyed by a competitor. On the positive side, others might benefit from enjoying witty conversations with us and from our increased taxes.

If in the case of intelligence enhancement the positive externalities outweigh the negative ones, then a prima facie case exists not only for permitting genetic enhancements aimed at increasing intellectual ability, but for encouraging and subsidizing them too. Whether such policies remain a good idea when all practicalities of implementation and political realities are taken into account is another matter. But at least we can conclude that an enhancement that has both significant intrinsic benefits for an enhanced individual and net positive externalities for the rest of society should be encouraged. By contrast, enhancements that confer only positional advantages, such as augmentation of stature or physical attractiveness, should not be socially encouraged, and we might even attempt to make a case for social policies aimed at reducing expenditure on such goods, for instance through a progressive tax on consumption.9

6. The Issue of Equality

One important kind of externality in germ-line enhancements is their effects on social equality. This has been a focus for many opponents of germ-line genetic engineering who worry that it will widen the gap between haves and have-nots. Today, children from wealthy homes enjoy many environmental privileges, including access to better schools and social networks. Arguably, this constitutes an inequity against children from poor homes. We can imagine scenarios where such inequities grow much larger thanks to genetic interventions that only the rich can afford, adding genetic advantages to the environmental advantages already benefiting privileged children. We could even speculate about the members of the privileged stratum of society eventually enhancing themselves and their offspring to a point where the human species, for many practical purposes, splits into two or more species that have little in common except a shared evolutionary history.10 The genetically privileged might become ageless, healthy, super-geniuses of flawless physical beauty, who are graced with a sparkling wit and a disarmingly self-deprecating sense of humor, radiating warmth, empathetic charm, and relaxed confidence. The non-privileged would remain as people are today but perhaps deprived of some their self-respect and suffering occasional bouts of envy. The mobility between the lower and the upper classes might disappear, and a child born to poor parents, lacking genetic enhancements, might find it impossible to successfully compete against the super-children of the rich. Even if no discrimination or exploitation of the lower class occurred, there is still something disturbing about the prospect of a society with such extreme inequalities.

While we have vast inequalities today and regard many of these as unfair, we also accept a wide range of inequalities because we think that they are deserved, have social benefits, or are unavoidable concomitants to free individuals making their own and sometimes foolish choices about how to live their lives. Some of these justifications can also be used to exonerate some inequalities that could result from germ-line engineering. Moreover, the increase in unjust inequalities due to technology is not a sufficient reason for discouraging the development and use of the technology. We must also consider its benefits, which include not only positive externalities but also intrinsic values that reside in such goods as the enjoyment of health, a soaring mind, and emotional well-being.

We can also try to counteract some of the inequality-increasing tendencies of enhancement technology with social policies. One way of doing so would be by widening access to the technology by subsidizing it or providing it for free to children of poor parents. In cases where the enhancement has considerable positive externalities, such a policy may actually benefit everybody, not just the recipients of the subsidy. In other cases, we could support the policy on the basis of social justice and solidarity.

Even if all genetic enhancements were made available to everybody for free, however, this might still not completely allay the concern about inequity. Some parents might choose not to give their children any enhancements. The children would then have diminished opportunities through no fault of their own. It would be peculiar, however, to argue that governments should respond to this problem by limiting the reproductive freedom of the parents who wish to use genetic enhancements. If we are willing to limit reproductive freedom through legislation for the sake of reducing inequities, then we might as well make some enhancements obligatory for all children. By requiring genetic enhancements for everybody to the same degree, we would not only prevent an increase in inequalities but also reap the intrinsic benefits and the positive externalities that would come from the universal application of enhancement technology. If reproductive freedom is regarded as too precious to be curtailed, then neither requiring nor banning the use of reproductive enhancement technology is an available option. In that case, we would either have to tolerate inequities as a price worth paying for reproductive freedom or seek to remedy the inequities in ways that do not infringe on reproductive freedom.

All of this is based on the hypothesis that germ-line engineering would in fact increase inequalities if left unregulated and no countermeasures were taken. That hypothesis might be false. In particular, it might turn out to be technologically easier to cure gross genetic defects than to enhance an already healthy genetic constitution. We currently know much more about many specific inheritable diseases, some of which are due to single gene defects, than we do about the genetic basis of talents and desirable qualities such as intelligence and longevity, which in all likelihood are encoded in complex const
ellations of multiple genes. If this turns out to be the case, then the trajectory of human genetic enhancement may be one in which the first thing to happen is that the lot of the genetically worst-off is radically improved, through the elimination of diseases such as Tay Sachs, Lesch-Nyhan, Downs Syndrome, and early-onset Alzheimers disease. This would have a major leveling effect on inequalities, not primarily in the monetary sense, but with respect to the even more fundamental parameters of basic opportunities and quality of life.

7. Are Germ-Line Interventions Wrong Because They Are Irreversible?

Another frequently heard objection against germ-line genetic engineering is that it would be uniquely hazardous because the changes it would bring are irreversible and would affect all generations to come. It would be highly irresponsible and arrogant of us to presume we have the wisdom to make decisions about what should be the genetic constitutions of people living many generations hence. Human fallibility, on this objection, gives us good reason not to embark on germ-line interventions. For our present purposes, we can set aside the issue of the safety of the procedure, understood narrowly, and stipulate that the risk of medical side-effects has been reduced to an acceptable level. The objection under consideration concerns the irreversibility of germ-line interventions and the lack of predictability of its long-term consequences; it forces us to ask if we possess the requisite wisdom for making genetic choices on behalf of future generations.

Human fallibility is not a conclusive ground for resisting germ-line genetic enhancements. The claim that such interventions would be irreversible is incorrect. Germ-line interventions can be reversed by other germ-line interventions. Moreover, considering that technological progress in genetics is unlikely to grind to an abrupt halt any time soon, we can count on future generations being able to reverse our current germ-line interventions even more easily than we can currently implement them. With advanced genetic technology, it might even be possible to reverse many germ-line modifications with somatic gene therapy, or with medical nanotechnology.11 Technologically, germ-line changes are perfectly reversible by future generations.

It is possible that future generations might choose to retain the modifications that we make. If that turns out to be the case, then the modifications, while not irreversible, would nevertheless not actually be reversed. This might be a good thing. The possibility of permanent consequences is not an objection against germ-line interventions any more than it is against social reforms. The abolition of slavery and the introduction of general suffrage might never be reversed; indeed, we hope they will not be. Yet this is no reason for people to have resisted the reforms. Likewise, the potential for everlasting consequences, including ones we cannot currently reliably forecast, in itself constitutes no reason to oppose genetic intervention. If immunity against horrible diseases and enhancements that expand the opportunities for human growth are passed on to subsequent generations in perpetuo, it would be a cause for celebration, not regret.

There are some kinds of changes that we need be particularly careful about. They include modifications of the drives and motivations of our descendants. For example, there are obvious reasons why we might think it worthwhile to seek to reduce our childrens propensity to violence and aggression. We would have to take care, however, that we do not do this in a way that would make future people overly submissive or complacent. We can conceive of a dystopian scenario along the lines of Brave New World, in which people are leading shallow lives but have been manipulated to be perfectly content with their sub-optimal existence. If the people transferred their shallow values to their children, humanity could get permanently stuck in a not-very-good state, having foolishly changed itself to lack any desire to strive for something better. This outcome would be dystopian because a permanent cap on human development would destroy the transhumanist hope of exploring the post-human realm. Transhumanists therefore place an emphasis on modifications which, in addition to promoting human well-being, also open more possibilities than they close and which increase our ability to make subsequent choices wisely. Longer active lifespans, better memory, and greater intellectual capacities are plausible candidates for enhancements that would improve our ability to figure out what we ought to do next. They would be a good place to start.12

Notes

1. See Eric K. Drexler, Nanosystems: Molecular Machinery, Manufacturing, and Computation (New York: John Wiley & Sons, Inc., 1992); Ray Kurzweil, The Age of Spiritual Machines: When Computers Exceed Human Intelligence (New York: Viking, 1999); Hans Moravec, Robot: Mere Machine to Transcendent Mind. (New York: Oxford University Press, 1999).

2. See Robert A. Freitas Jr., Nanomedicine, Volume 1: Basic Capabilities (Georgetown, Tex.: Landes Bioscience, 1999).

3. See Robert Ettinger, The Prospect of Immortality (New York: Doubleday, 1964); James Hughes, The Future of Death: Cryonics and the Telos of Liberal Individualism, Journal of Evolution and Technology 6 (2001).

4. See Eric K. Drexler, Engines of Creation: The Coming Era of Nanotechnology (London: Fourth Estate, 1985).

5. See David Lewis, Dispositional Theories of Value, Proceedings of the Aristotelian Society Supp. 63 (1989).

6. See Erik Parens, ed., Enhancing Human Traits: Ethical and Social Implications. (Washington, D. C: Georgetown University Press, 1998).

7. See Leon Kass, Life, Liberty, and Defense of Dignity: The Challenge for Bioethics (San Francisco: Encounter Books, 2002).

8. See Jonathan Glover, What Sort of People Should There Be? (New York: Penguin, 1984); Gregory Stock, Redesigning Humans: Our Inevitable Genetic Future (New York, Houghton Mifflin, 2002); and Allen Buchanan et al., From Chance to Choice: Genetics & Justice (Cambridge, England: Cambridge University Press, 2002).

9. See Robert H. Frank, Luxury Fever: Why Money Fails to Satisfy in an Era of Excess (New York: Free Press, 1999).

10. Cf. Lee M. Silver, Remaking Eden: How Genetic Engineering and Cloning will Transform the American Family (New York: Avon Books, 1997); and Nancy Kress, Beggars in Spain (Avon Books, 1993).

11. See Freitas, op. cit.

12. For their helpful comments I am grateful to Heather Bradshaw, Robert A. Freitas Jr., James Hughes, Gerald Lang, Matthew Liao, Thomas Magnell, David Rodin, Jeffrey Soreff, Mike Treder, Mark Walker, Michael Weingarten, and an anonymous referee of the Journal of Value Inquiry.

Excerpt from:
Human Genetic Enhancements: A Transhumanist Perspective

Human Genetic Engineering: A Guide for Activists, Skeptics …

Pete Shanks has written a terrific introduction to human genetic engineering and the fraught issues it raises. The basic question he takes on: How do we get what's good out of human biotechnology, but make sure we don't wake up one morning and find ourselves in GATTACA?

"Guide to Human Genetic Engineering" covers the cloning of people and pets, "transhumanism," eugenics, sex selection, designer babies, gene doping, stem cells, and more. It welcomes beneficial uses of biotechnology, but cuts through the techno-boosterism that characterizes far too much of the current public discussion of these issues.

The book's appearance is engaging, with a table or pull quote or something else visually interesting on almost every page. The writing is top-notch -- entertaining, even funny and intermittently irreverent, but without ever losing sight of the seriousness and importance of the subject matter. The author clearly explains the technical basics, and goes beneath the surface of the political and social controversies, but not so deep as to lose "perplexed" or simply curious readers. He makes it clear what he thinks, but it's obvious that he respects what others think too.

I recommend this book very highly.

Link:
Human Genetic Engineering: A Guide for Activists, Skeptics ...

Five technologies that may alter India in 2020 – Livemint

Bengaluru: What must it have felt like to be a cotton spinner or an iron maker in England in the 1820s in the midst of an industrial revolution? Exactly 200 years later, we may be on the verge of another era of momentous change: the internet revolution. With internet access expanding dramatically post the early 1990s, a slew of new technologies have now matured to a point where fundamental change constantly seems to be right around the corner.

On the doorstep of a brand new decadethe 2020swhat new frontiers may Artificial Intelligence (AI) or gene editing open up? Will we soon have robot bosses? Will mixed reality change the way we consume entertainment and sports? Will we be able to cure 90% of all genetic diseases by the end of the decade? We take a look at five technologies that could alter India and the world. This may not be a definitive or even exhaustive list, but it is a list of things that could change the way we live, work, and play sooner than we think.

Mixed reality

Imagine watching a football match, not on your TV but on a virtual reality (VR) headset that streams the match live and projects interesting stats on the fly with the help of augmented reality (AR). Mumbai-based VR startup Tesseract, now owned by Mukesh Ambanis Reliance Jio, is promising a future like that with its Quark camera, Holoboard headset, and the high internet speeds of Jio Fiber. Similarly, a Hyderabad-based mixed reality startup called Imaginate enables cross-device communication over VR and AR wearables for better enterprise collaboration in the industrial sector.

Despite the much-hyped yet unmet expectations from the likes of Google Glass, Microsoft HoloLens and Facebooks Oculus, Tesseract and Imaginate simply underscore how the fusion of AR and VR technologies the combination of which is popularly known as Mixed Reality or MR is coming of age and is no longer in the realm of just sci-fi movies like Blade Runner 2049, where Officer K played by Ryan Gosling develops a relationship with his artificial intelligence (AI) hologram companion Joi.

For instance, AI-powered chatbots today can not only conduct a conversation in natural language via audio or text but they can be made more powerful with a dose of mixed reality. Last May, Fidelity Investments created a prototype VR financial advisor named Cora to answer client queries using a suite of tools from Amazon Web Services. Researchers in Southampton have built a device that displays 3D animated objects that can talk and interact with onlookers.

The Chinese government-run Xinhua News Agency has the worlds first AI-powered news anchor, whose voice has been modelled to resemble a real human anchor working for the agency. Going a step further, Japan-headquartered DataGrid Inc. uses generative adversarial networks (GANs) to develop its so-called whole body model automatic generation AI" that automatically generates full-length images of non-existent people with high resolutions.

Nevertheless, challenges abound when dealing MR-and AI-powered robots, humanoids, and human avatars. For one, whenever a company generates human bodies and faces, concerns over deep fakes and cheap fakes will always rear their heads. Second, data collection will continually raise concerns over security and privacy. Third, theres always the concern regarding the fairness of an AI algorithm when it is deployed to do human tasks like giving financial advice. Last, but not the least, theres also the question of whether AI bots should be allowed to pose as humans. This will continually pose a challenge and opportunity for technologists and policy makers.

Future of solar

Heliogen, a company that has billionaire philanthropist Bill Gates as one of its investors, says it has created the worlds first technology that can commercially replace fuels with carbon-free, ultra-high temperature heat from the sun. With its patented technology, Heliogens field of mirrors acts as a multi-acre magnifying glass to concentrate and capture sunlight.

This is just a case in point that solar technologies have evolved a lot since they first made their debut in the 1960s. For instance, solar roadwayspanels lining the surface of highwayshave already popped up in the Netherlands. Floating solar, on its part, is providing a credible option to address land use concerns associated with wide scale solar implementations. A French firm called Ciel et Terre, for instance, has projects set up in France, Japan, and England. Other parts of the world, including India and California in the US, are piloting similar floating solar initiatives.

Space-based solar technology is another exciting arena. India, China and Japan are investing heavily in these technologies right now. The Japan Aerospace Exploration Agencys (JAXA) Space Solar Power Systems (SSPS) aims to transmit energy from orbiting solar panels by 2030. Further, researchers at the VTT Technical Research Centre in Finland have used solar and 3D printing technologies to develop prototypes of what they have christened as energy harvesting trees".

With solar power cheaper than coal in most countries in the world, its worth scaling up these technologies.

Indians and robot bosses

Between 400 and 800 million individuals around the world could be displaced by automation and would need to find new jobs by 2030, predicted a December 2017 survey by consultancy firm McKinsey. The Future of Jobs 2018 report by the World Economic Forum (WEF) suggests that 75 million jobs may be lost to automation by 2022, but adds that another 133 million additional new roles will be created.

Given that many of the automated jobs are being taken away by AI-powered chatbots and intelligent robots, would humans eventually have to work for a robo boss? This, however, may not be as big a concern as it is made out to be. According to the second annual AI at Work study conducted by Oracle and Future Workplace, people trust robots more than their managers. The study, released this October, notes that workers in China (77%) and India (78%) have adopted AI over 2X more than those in France (32%) and Japan (29%). Further, workers in India (60%) and China (56%) are the most excited about AI, while men have a more positive view of AI at work than women.

Oracle and Future Workplace also found that 82% of the workers believe robot managers are better at certain tasks, such as maintaining work schedules and providing unbiased information, than their human counterparts. And almost two-thirds (64%) of workers worldwide say they would trust a robot more than their human manager. In China and India, that figure rises to almost 90%.

On the other hand, the respondents felt managers can outdo robots when it comes to understanding their feelings, coaching them, and creating a healthy work culture. Whether humans eventually serve a robo boss or not remains to be seen. However, we can be certain of one thing: in the near future, we will increasingly see humans collaborating with smart robots.

Future of payments

Everyone can be a merchant, and every device can be an acceptance device," Accenture noted in its 2017 Driving the Future of Payments report. This trend has only accelerated over the last two years, especially with banks coming to terms with the fact that young customers, especially those living in urban areas, prefer net banking and mobile banking and would seldom, or never, want to visit a bank branch if offered that choice.

Bitcoin and cryptocurrency investors, for instance, have not lost faith in this disruptive currency despite the run with volatility, and despite the industry being viewed with a lot of suspicion by most governments around the world, including India. Fintechs too, with their innovative technology solutions like AI-powered bots and contactless payments to name a few, have only made the payments ecosystem more inclusive, disruptive, and challenging. In India, especially, the governments Aadhaar-enabled payments system and the Unified Payments Interface (UPI) have revolutionized the payments ec
osystem. The total volume of UPI transactions in the third quarter of calendar 2019 touched 2.7 billiona 183% rise over the same July-September quarter a year ago. In terms of value, UPI clocked 4.6 trillionup 189% over the same period a year ago, according to the Worldlines India Digital Payments Report-Q3 2019.

However, the number of transactions done on mobile wallets was 1.04 billiononly a 5% rise over the previous year period.

QR codes, according to the report, will continue to be used for payments, and the internet of things (IoT) is set to dominate micro payments by transforming connected devices into payment channels, though the pace of adoption of 5G by countries like India will be the key.

Nevertheless, cash that has been in existence for over 3000 years in different forms is not going to disappear in a hurry. Trust and security will continue to remain the operative words in digital payments.

Making sense of gene editing

When Dolly the sheep made news for becoming the first mammal ever to be cloned from another individuals body cell, many expected human cloning to follow soon. Dolly died over 16 years ago, and subsequently animals, including monkeys and dogs, continue to be cloned successfully. Yet, no human being has yet been cloned in real life.

While human cloning, which may or may not eventually happen, is bound to raise a lot of alarm bells given the moral implications surrounding the issue, the fact is that human genomes, or genes, are being routinely edited in a bid to find solutions for what are today considered to be incurable genetically inherited diseases.

Researchers are using a gene editing tool known as CRISPR-Cas9. CRISPR, which stands for Clusters of Regularly Interspaced Short Palindromic Repeats, is a tool that allows researchers to easily alter DNA sequences and modify gene function. The protein Cas9 (CRISPR-associated, or Cas) is an enzyme that acts like a pair of molecular scissors capable of cutting strands of DNA.

CRISPR-Cas9 is primarily known for its use in treating diseases like AIDS, amyotrophic lateral sclerosis (ALS), and Huntingtons disease. Two patients, one with beta thalassemia and one with sickle cell disease, have potentially been cured of their diseases, reveal results from clinical trials that were jointly conducted by Vertex Pharmaceuticals and CRISPR Therapeutics. The results released this November involved using Crispr to edit the genes of these patients.

Researchers are now looking to extend its use to tackle famine, lend a hand in creating antibiotics, and even wipe out an entire species such as malaria-spreading mosquitoes. Further, by genetically engineering a persons bone marrow cells, researchers can reprogram their immune and circulatory systems. Some new cancer treatments are based on this. Moreover, looking at the DNA of the collection of microbes in your gut can help with digestive disorders, weight loss, and even help understand mood changes.

Closer home, scientists at the Institute of Genomics and Integrative Biology (IGIB) and the Indian Institute of Chemical Biology (CSIR-IICB) are trying to correct genetic mutations in their laboratories using CRISPR Cas9 with encouraging preliminary results. But due to regulatory and ethical concerns, it may take a while before they can use this on humans.

IGIB also sells CRISPR products such as Cas9 proteins and its variants to educational institutes at reduced prices in a bid to encourage use of the technology.

The US Food and Drug Administration (FDA), on its part, considers any use of CRISPR-Cas9 gene editing in humans to be gene therapy and rules that the sale of DIY kits to produce gene therapies for self-administration is illegal. India, too, has banned the use of stem cell therapy for commercial use following concerns over rampant malpractice".

CRISPR-Cas9, thus, remains a work in progress and countries should have policies to govern its use. Meanwhile, one can watch out for an upgrade to CRISPR called Prime, which theoretically has the ability to snip out more than 90% of all genetic diseases.

Originally posted here:
Five technologies that may alter India in 2020 - Livemint

How Gene Editing Is Changing the World – The Wire

Across the US, more than 100,000 people are awaiting organ transplants. But there simply arent enough hearts, lungs, livers, and kidneys to meet demand, and 20 people die every day without the organs they need. For decades, scientists have dreamed of using animals to help fill the gap. Theyve been particularly interested in harvesting organs from pigs, whose physiology is similar to our own. Unfortunately, pigs also present some big biological challenges, including the fact that their genomes are chock full of genes that code for what are known as retroviruses, which could pose a serious threat to patients who receive porcine organs.

In 2015, George Church, a geneticist at Harvard University, announced a stunning breakthrough: Working with pig cells, he and his colleagues had managed to disable 62 copies of a retrovirus gene in one fell swoop. This would have been virtually impossible and a logistical nightmare with older forms of genetic modification, writes Nessa Carey in her new book, Hacking the Code of Life: How Gene Editing Will Rewrite Our Futures. But by using the new gene editing technology known as Crispr, the task was a relative cinch.

Nessa CareyHacking the Code of LifeIcon Books

Its just one example of how gene editing is giving us the power to alter the genome with unprecedented speed and precision. Carey, a biologist with a background in the biotech and pharmaceutical industry, offersa brisk, accessible primer on the fast-moving field, a clear-eyed look at a technology that is already driving major scientific advances and raising complex ethical questions

Its giving every biologist in the world the tools to answer in a few months questions that some scientists have spent half their careers trying to address, Carey writes. Its fueling new ways to tackle problems in fields as diverse as agriculture and cancer treatments. Its a story that began with curiosity, accelerated with ambition, will make some individuals and institutions extraordinarily wealthy, and will touch all our lives.

Though there are several different approaches to gene editing, the most prominent and the one that really supercharged the field is Crispr. The technique, based on an anti-viral defence system thats naturally present in bacteria, requires two pieces of biological material: an enzyme that acts as a pair of minuscule scissors, slicing strands of DNA in two; and a guide molecule that tells the enzyme where to cut.

In bacteria, these guide molecules direct the enzyme to chop up the genomes of invading viruses, preventing them from replicating.

But in 2012 and 2013, two teams of scientists reported that it was possible to hack this system to slice into any strand of DNA, at any complementary location they chose. Researchers could, for instance, create a guide molecule that steered the enzyme to one specific gene in the mouse genome and insert the editing machinery into a mouse cell; the enzyme would then make its cut at that exact spot.

Also Read: Is There More to Gene Editing Than Creating Designer Humans?

The cell would repair the severed DNA, but it would do so imperfectly, disabling the gene in question. In the years that followed, scientists refined the technique, learning to use it not only to inactivate genes but also to insert new genetic material at specific locations along the genome.

The approach is cheaper, easier, and faster than older methods of genetic engineering, which were first developed in the 1970s. In addition, as Carey explains, it can be used to create smaller modifications to the genome, and leaves fewer extraneous genetic elements. In its most technically exquisite form, gene editing leaves no molecular trace at all. It may just change, in a precisely controlled manner, one letter of the genetic alphabet.

But in 2012 and 2013, two teams of scientists reported that it was possible to slice into any strand of DNA. Photo: qimono/pixabay

The applications are almost endless. Gene editing has immense potential for basic research; scientists can learn a lot about what genes do by selectively disabling them. In addition, researchers have used the technology to create a wide variety of organisms that could become valuable agricultural commodities, including mushrooms that dont brown; wheat that produces fewer gluten proteins; drought tolerant, high-yield rice and corn; disease-resistant pigs; and super muscular goats.

How these products will do on the market if they ever reach it remains uncertain. Globally, gene-edited organisms are regulated by a patchwork of conflicting rules. For instance, in 2018, the US Department of Agriculture announced that it would not regulate gene-edited crops that could otherwise have been developed through traditional breeding techniques. A few months later, however, the European Union said that it would subject gene-edited plants to stringent restrictions.

Beyond agriculture, gene editing has enormous potential for medicine. It might, for instance, become a much-needed treatment for sickle cell disease. That painful, debilitating disease results from a genetic mutation that causes patients to produce a deformed version of haemoglobin, a protein that helps red blood cells transport oxygen. In a clinical trial currently underway, scientists are removing stem cells from the bone marrow of sickle cell patients, using Crispr to edit them, and then infusing the edited cells back into patients.

Also Read: Explainer: What Is CRISPR and How Does It Work?

Even if this trial succeeds, however, gene editing will not be a cure-all. It doesnt always work perfectly and can be challenging to administer directly to living humans (which is why some scientists are instead editing patients cells outside the body). Moreover, many diseases are caused by complex interactions between multiple genes, or genes and the environment. In fact, many of the most common and debilitating conditions arent likely to be good candidates for gene editing any time soon, Carey writes.

And, of course, the ethics of human gene editing can be enormously fraught. Thats especially true when scientists modify sperm cells, egg cells, or early embryos, making tweaks that could be passed down to subsequent generations. This kind of gene editing could theoretically cure some absolutely devastating genetic conditions, but we still have a lot to learn about its safety and effectiveness. It also raises a host of difficult questions about consent (an embryo obviously cannot give it), inequality (who will have access to the technology?), and discrimination (what will the ability to edit a gene related to deafness mean for deaf people, deaf culture, and the disability rights movement more broadly?).

Even in the face of these questions, at least one scientist has already forged ahead. In November 2018, He Jiankui, a researcher then at the Southern University of Science and Technology in China, shocked the world by announcing that the worlds first gene-edited babies twin girls, who He called Nana and Lulu had already been born. Months earlier, when Nana and Lulu were just embryos, He had edited their CCR5 genes, which code for a protein that allows HIV to infect human cells. By disabling the gene, He hoped to engineer humans who would be protected from HIV infection.

Also Read: How a Rogue Chinese Experiment Might Affect Gene-Based Therapies in India

The outcry was swift and harsh. Scientists alleged that Hes science was sloppy and unethical, putting two human beings at unnecessary risk. After all, there are already plenty of ways to prevent HIV transmission, and the CCR5 protein is known to have some benefits, including protecting against the flu. And He had raced ahead of the experts who were still trying to work out careful ethical guidelines for editing human embryos. He Jiankui has shot this measured approach to pieces with his announcement, and now the rest of the scientific community is on the back foot, trying to reassure the public and to create consensus rapidly, Carey writes.

Scientist He Ji
ankui attends the International Summit on Human Genome Editing at the University of Hong Kong on November 28, 2018. Photo: REUTERS/Stringer/File Photo

Hacking the Code of Lifedoesnt break much new ground, and for readers who have been paying attention to Crispr over the past few years, little in the book will come as a surprise. But it does provide a broad, even-handed overview of how much has already happened in a field that is less than ten years old.

Carey swats down the most dystopian dreams about Crispr, like the prospect that criminals might edit their own DNA to evade justice. Shes similarly skeptical that well end up using the technology to create super-beings with enhanced genomes that will make them taller, faster, more attractive.

We actually understand very little about the genetic basis of these traits and what we do know suggests that it will be very difficult to enhance humans in this way, she writes.

But she also acknowledges real risks, including the possibility that the technique could be used to create dangerous bioweapons, that gene-edited organisms could destabilise natural ecosystems, and that our new, hardy crops could prompt us to convert even more of the Earths undeveloped places into farmland.

None of this means that the technology should be abandoned; it has immense potential to improve our lives, as the book makes clear. But it does mean we need to proceed with caution. As Carey writes, Ideally, ethics should not be dragged along in the wake of scientific advances; the two should progress together, informing one another.

Emily Anthes, who has written for Undark, The New York Times, The New Yorker, Wired, and Scientific American, among other publications, is the author of the forthcoming book The Great Indoors.

This article was originally published on Undark. Read the original article.

Link:
How Gene Editing Is Changing the World - The Wire

Pros and Cons of Genetic Engineering – Conserve Energy Future

Genetic engineering is the process to alter the structure and nature of genes in human beings, animals or foods using techniques like molecular cloning and transformation. In other words, it is the process of adding or modifying DNA in an organism to bring about great deal of transformation.

Genetic engineering was thought to be a real problem just a few short years ago. We feared that soon we would be interfering with nature, trying to play God and cheat him out of his chance to decide whether we were blonde or dark haired, whether we had blue or bright green eyes or even how intelligent we were. The queries and concerns that we have regarding such an intriguing part of science are still alive and well, although they are less talked about nowadays than they were those few years ago.

However, this does not mean that they are any less relevant. In fact, they are as relevant today as they ever were. There are a number of very real and very troubling concerns surrounding genetic engineering, although there are also some very real benefits to further genetic engineering and genetic research, too. It seems, therefore, as though genetic engineering is both a blessing and a curse, as though we stand to benefit as well as lose from developing this area of science even further.

With genetic engineering, we will be able to increase the complexity of our DNA, and improve the human race. But it will be a slow process, because one will have to wait about 18 years to see the effect of changes to the genetic code.Stephen Hawking

Although at first the pros of genetic engineering may not be as apparent as the cons, upon further inspection, there are a number of benefits that we can only get if scientists consider to study and advance this particular branch of study. Here are just a few of the benefits:

1. Tackling and Defeating Diseases

Some of the most deadly and difficult diseases in the world, that have so resisted destruction, could be wiped out by the use of genetic engineering. There are a number of genetic mutations that humans can suffer from that will probably never be ended unless we actively intervene and genetically engineer the next generation to withstand these problems.

For instance, Cystic Fibrosis, a progressive and dangerous disease for which there is no known cure, could be completely cured with the help of selective genetic engineering.

2. Getting Rid of All Illnesses in Young and Unborn Children

There are very many problems that we can detect even before children are born. In the womb, doctors can tell whether your baby is going to suffer from sickle cell anemia, for instance, or from Down s syndrome. In fact, the date by which you can have an abortion has been pushed back relatively late just so that people can decide whether or not to abort a baby if it has one or more of these sorts of issues.

However, with genetic engineering, we would no longer have to worry. One of the main benefit of genetic engineering is that it can help cure and diseases and illness in unborn children. All children would be able to be born healthy and strong with no diseases or illnesses present at birth. Genetic engineering can also be used to help people who risk passing on terribly degenerative diseases to their children.

For instance, if you have Huntingtons there is a 50% chance that your children with inherit the disease and, even if they do not, they are likely to be carriers of the disease. You cannot simply stop people from having children if they suffer from a disease like this, therefore genetic engineering can help to ensure that their children live long and healthy lives from either the disease itself or from carrying the disease to pass on to younger generations.

3. Potential to Live Longer

Although humans are already living longer and longer in fact, our lifespan has shot up by a number of years in a very short amount of time because of the advances of modern medical science, genetic engineering could make our time on Earth even longer. There are specific, common illnesses and diseases that can take hold later in life and can end up killing us earlier than necessary.

With genetic engineering, on the other hand, we could reverse some of the most basic reasons for the bodys natural decline on a cellular level, drastically improving both the span of our lives and the quality of life later on. It could also help humans adapt to the growing problems of, for instance, global warming in the world.

If the places we live in become either a lot hotter or colder, we are going to need to adapt, but evolution takes many thousands of years, so genetic engineering can help us adapt quicker and better.

4. Produce New Foods

Genetic engineering is not just good for people. With genetic engineering we can design foods that are better able to withstand harsh temperatures such as the very hot or very cold, for instance and that are packed full of all the right nutrients that humans and animals need to survive. We may also be able to make our foods have a better medicinal value, thus introducing edible vaccines readily available to people all over the world

Perhaps more obvious than the pros of genetic engineering, there are a number of disadvantages to allowing scientists to break down barriers that perhaps are better left untouched. Here are just a few of those disadvantages:

1. Is it Right?

When genetic engineering first became possible, peoples first reactions were to immediately question whether it was right? Many religions believe that genetic engineering, after all, is tantamount to playing God, and expressly forbid that it is performed on their children, for instance.

Besides the religious arguments, however, there are a number of ethic objections. These diseases, after all, exist for a reason and have persisted throughout history for a reason. Whilst we should be fighting against them, we do need at least a few illnesses, otherwise we would soon become overpopulated. In fact, living longer is already causing social problems in the world today, so to artificially extend everybodys time on Earth might cause even more problems further down the line, problems that we cannot possibly predict.

2. May Lead to Genetic Defects

Another real problem with genetic engineering is the question about the safety of making changes at the cellular level. Scientists do not yet know absolutely everything about the way that the human body works (although they do, of course, have a very good idea). How can they possibly understand the ramifications of slight changes made at the smallest level?

What if we manage to wipe out one disease only to introduce something brand new and even more dangerous? Additionally, if scientists genetically engineer babies still in the womb, there is a very real and present danger that this could lead to complications, including miscarriage (early on), premature birth or even stillbirth, all of which are unthinkable.

The success rate of genetic experiments leaves a lot to be desired, after all. The human body is so complicated that scientists have to be able to predict what sort of affects their actions will have, and they simply cannot account for everything that could go wrong.

3. Limits Genetic Diversity

We need diversity in all species of animals. By genetically engineering our species, however, we will be having a detrimental effect on our genetic diversity in the same way as something like cloning would. Gene therapy is available only to the very rich and elite, which means that traits that tend to make people earn less money would eventually die out.

4. Can it Go Too Far?

One pressing question and issue with genetic engineering that has been around for years and years is whether it could end up going too far. There are many thousands of genetic scientists with honest intentions who want to bring an end to the worst diseases and illnesses of the current century and who are trying to do so by using genetic engineering.

Ho
wever, what is to stop just a handful of people taking the research too far? What if we start demanding designer babies, children whose hair color, eye color, height and intelligence we ourselves dictate? What if we end up engineering the sex of the baby, for instance in China, where is it much more preferable to have a boy? Is that right? Is it fair? The problems with genetic engineering going too far are and ever present worry in a world in which genetic engineering is progressing further and further every day.

Genetic engineering is one of the topic that causes a lot of controversy. Altering the DNA of organisms has certainly raised a few eyebrows. It may work wonders but who knows if playing with the nature is really safe? Making yourself aware of all aspects of genetic engineering can help you to form your own opinion.

A true environmentalist by heart . Founded Conserve Energy Future with the sole motto of providing helpful information related to our rapidly depleting environment. Unless you strongly believe in Elon Musks idea of making Mars as another habitable planet, do remember that there really is no 'Planet B' in this whole universe.

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Pros and Cons of Genetic Engineering - Conserve Energy Future

Links for July 28, 2017: Outlining the GOP tax plan, the ethics of … – American Enterprise Institute

GOP lawmakers, White House outline tax plan WSJ

The final blow [to the Border Adjustment Tax] came Thursday, in a broad statement of principles released by party leaders to build Republican unity on tax policy and create momentum for advancing legislation this fall.

The statement emphasized a common goal of reducing individual and corporate rates and individual tax rates as much as possible. It also called for faster writeoffs for capital expenses, an idea meant to promote investment, though it stopped short of a House Republican proposal for immediate writeoffs.

The shared principles in effect represent a starting point for the approaching debate. Party leaders willingness to release a framework is also a sign of their confidence in getting a bill written and passed.

Still, Thursdays statement left critical questions unanswered, such as how much individual and corporate rates would be cut, and avoided addressing many of the tough trade-offs Republicans would need to make to achieve substantial reductions in tax rates, such as what deductions to eliminate.

Taken together, it included less detail than President Donald Trumps campaign plan, the House GOPs June 2016 blueprint or the one-page White House offering in April.

Shell prepares for lower forever oil prices WSJ

Read more on this, here.

Unions urge slow-down as self-driving car laws pick up speed Bloomberg

A simple way to help low-income students: Make everyone take the SAT NYT

And now the weeks eeriest news, with some reactions:

First human embryos edited in the US Technology Review

Until now, American scientists have watched with a combination of awe, envy, and some alarm as scientists elsewhere were first to explore the controversial practice. To date, three previous reports of editing human embryos were all published by scientists in China.

Now Mitalipov is believed to have broken new ground both in the number of embryos experimented upon and by demonstrating that it is possible to safely and efficiently correct defective genes that cause inherited diseases.

Although none of the embryos were allowed to develop for more than a few daysand there was never any intention of implanting them into a wombthe experiments are a milestone on what may prove to be an inevitable journey toward the birth of the first genetically modified humans.

We need to talk about genetic engineering Commentary

It is incumbent upon Americans of all political stripesnot just conservatives or the faithfulto consider the moral implications of embryonic genetic engineering. In April of 2015, National Institutes of Health Director Dr. Francis Collins issued a statement pledging that NIH will not fund any use of gene-editing technologies in human embryos, but this prohibition does not apply to private endeavors. Public ethos guides private industry, but what is public philosophy regarding the interference with genetic destiny?

Are we obliged to eradicate genetic disorders? Is it unethical not to intervene in the development of an embryo if we have the capacity to alleviate future suffering and hardship? Is it morally questionable to select for various cosmetic traits that prospective parents might find desirable? Do we engage in this process of upending the natural order without knowing the long-term effects of genetic manipulation? Is a modified population a form of eugenics?

If you could design your own child, would you? The Washington Post

We have arrived at a Rubicon. Humans are on the verge of finally being able to modify their own evolution. The question is whether they can use this newfound superpower in a responsible way that will benefit the planet and its people. And a decision so momentous cannot be left to the doctors, the experts or the bureaucrats.

Failing to figure out how to ensure that everyone will benefit from this breakthrough risks the creation of a genetic underclass who must struggle to compete with the genetically modified offspring of the rich. And failing to monitor and contain how we use it may spell global catastrophe. Its up to us collectively to get this right.

Gene editing: new technology, old moral questions The New Atlantis

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Links for July 28, 2017: Outlining the GOP tax plan, the ethics of ... - American Enterprise Institute

Gene technology raises ethical questions – Pacific Coast Business Times

By Frank Kalman

A relatively obscure talk about genes was given at UC Santa Barbara recently by Dr. Siddhartha Mukherjee, a researcher and clinical oncologist at Columbia University and author of a Pulitzer Prize winning book, the Emperor of all Maladies: A Biography of Cancer.

It was, however, on par in terms of gravity with talks many decades ago by the founders of the A-bomb, who espoused the benefits of radiation and harnessing the atom but also spoke of the dark side of splitting the atom.

Mukherjee spoke of engineering genes, of the huge life-saving potential but also of the dark side of gene manipulation.

He began by giving background on what a gene is: a unit of hereditary information that carries information to specify biological function. You might imagine genes as a set of master instructions carried between cells and between organisms that tell it how to build, maintain, repair and reproduce itself. It controls everything about us: the color of our eyes, our height and our intellect.

Mukherjee posed this question to the audience: If you knew your unborn child had an 80 percent chance of having autism, would you abort? Would you abort at 50 percent? At 25 percent?

Until recently, scientists were only able to determine if an embryo was predisposed to a serious disease. Now technologies are evolving, such as CRISPR, which allow scientists to edit malfunctioning genes causing these diseases.

Mukherjee discussed a recently released report from the National Academy of Sciences panel that proposes guidelines for gene editing. The report proposes that human embryo editing might be permissible if there are no other reasonable alternatives for treatment or prevention, the gene(s) being altered result in a serious disease or condition, or the genes cause or strongly predispose a person to that disease or condition.

Picture a woman told that she carries a mutation in her BRCA-1 gene, so she has a 60 to 70 percent chance of developing breast or ovarian cancer during her lifetime.

Concerned that this not be a burden for her unborn children and descendants, she seeks to have the mutated gene removed.

According to the NAS panel, she doesnt automatically qualify for genetic engineering. The conditions in the report are not absolutely clear and are subject to interpretation.

Then there is the issue of genetic engineering for the purpose of enhancement. This was the scariest part of Mukherjees entire presentation human enhancement to increase a childs muscle mass and athletic ability or to boost intelligence.

The NAS panels report is firmly against the use of gene editing for human enhancements but this is where Mukherjee raises red flags. He said the rich will have the ability to conduct the testing and pay for the genetic engineering not only to avoid disease but also for enhancements.

After 50 or 500 years of this, two groups of human beings will exist the enhanced and the unenhanced.

The NAS report encourages government bodies to conduct public discussion and policy debate. Gene editing truly requires smart and strong federal regulation. We are at a very critical juncture in the history of humanity, just like we were in the 1940s with the atom.

This new gene technology could not have presented itself at a worse time. The Trump administrations chief adviser, Stephen Bannon, recently told the Conservative Political Action Conference, If you look at these cabinet nominees, they were selected for a reason, and that is destruction, destruction of the administrative state. In other words, they were selected to destroy their respective regulatory agencies.

We must be extremely grateful for Mukherjees effort to ring the alarm bell in an effort to make us aware of this critical juncture in our history. There are extremely complicated ethical questions that require extremely thoughtful solutions. They will also require strongly enforced federal regulation.

Frank Kalman is the executive director of the Kids Cancer Research Foundation in San Luis Obispo. You can contact him at [emailprotected]

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Gene technology raises ethical questions - Pacific Coast Business Times

The perpetual journey of innovation – Enterprise Innovation

Four years ago, mega technology trends revolved around big data, the cloud, mobility, and the start of the Internet of Things (IoT). Fast forward to 2017, technology have been built on the foundation of these mega trends, and has seen a massive breakthrough with innovations that have and will continue to disrupt businesses, modernize economies and accelerate growth across industries.

As we journey through this year, we will see technology and our everyday lives be intertwined more than ever before, with organizations undergoing digital transformations at different scales across the world. The technology framework for the future is taking shape to revolutionize how we conduct businesses and take on new challenges in an increasing digitalized economy.

The question is, what is the endpoint to which we see technology being part of our lives? Lets take a simple example of fitness tracker devices embedded with IoT sensors. It can track your steps and exercise routines, sync it with your smartphone and translate all that data into insights on your progress. Pretty amazing, when it became mainstream in the late 2000s at least. But like many other technologies, we are starting to get used to moving on quite rapidly, wanting something better, more powerful, more useful. We crave for innovative technology simply because we can. Because of such rapid changes and our hunger for more, companies have been forced to accelerate innovation and pay more attention to preparing ourselves for the future. Which is why technology today has become increasingly scalable and easily adaptable to future environments. With software primarily at its core, its become nimble. So, to the earlier question, the simple answer is that there is no endpoint to what technology can offer in this day and age, and we must prepare ourselves for the perpetual journey of innovation.

With todays youths being the driving force for tomorrows economy, it is more pertinent now than ever before for youths to embrace new technology innovations, to be able to leverage technology effectively in the future. In fact, we recently conducted a survey of 1,400 youth across Asia Pacific to understand how they view their digital future, and what they found as the three most exciting technologies are Artificial Intelligence, Mixed Reality and Internet of Things.

The study also found that the top benefits they wanted out of these technologies were to help them increase their productivity, facilitate the way they connect with people and improve their physical and mental health. This indicates an understanding on the deeper impact they will have on our lives.

Let us take a closer look at these technologies that will continue to evolve and why they stand out as some of the most important in our future.

Artificial Intelligence

Artificial intelligence (AI) may still seem like stuff of science fiction for some of us, but it is already present in our everyday lives and work. And we are not talking about robots with limbs, but rather technology that can already understand what humans can do, like language, facial recognition, virtual personal assistants or predictive services like identifying what we like to read and making appropriate recommendations.

That said, AI is indeed evolving quickly and is now being used in much more advanced ways, and is being developed and run with even more precision to address deeper issues like healthcare, poverty, terrorism and autonomous vehicles. Today, self-driving cars are already being tested on roads in some cities, smart homes are being marketed, capabilities in biology and genetic engineering are starting to change not only human health and the healthcare industry, but also the way we think about and manage livestock.

Industries will need to continue to leverage machine learning as an ally rather than a threat (to potential job losses, for example). With AI capabilities driving their digital transformation initiatives in an expanding digital economy, AI will to gain more prominence, giving new meaning to automation and breaking grounds for real time solutions and powered by cloud technology.

Mixed Reality

For as long as one could remember, interactions with PCs, tablets and phones have always been a simple point and click, or touch and flick. The introduction of Mixed Reality devices has transformed the way we live, engage and connect. As physical and virtual worlds intersect in new ways, mixed reality allows for a more immersive experience for working remotely or supporting future workplaces to improve collaboration, and tackle organizational challenges anytime, from anywhere.

Beyond the immersive experience however, mixed reality has gone much further in redefining how we can break down geographical barriers. Think about NASAs Mars exploration project and how they have virtually brought Mars to Earth through mixed reality, for an entirely new way of exploration and learning experience.

Internet of Things

Internet of Things (IoT) continues to solicit indelible support from industries worldwide as businesses undergo digital transformation. The global IoT market is expected to reach USD724.2 billion by 2023, according to a report by Research Nester. With the proliferation of technology and rapid growth of urbanization, organizations will continue to adopt and adapt to new technological solutions that will drive business to new frontiers.

New IoT solutions will leverage AI and machine learning to interact with humans and the surroundings, such as drones, self-driving cars, smart kitchens/homes which will be increasingly integrated into daily living.

IoT will also push businesses a step further by offering them immeasurable insights into customers minds, and organizations will be able to create, change and ensure customers value from these insights.

Looking Ahead

We can only look forward to an exciting and smarter future, with many technologies inevitably shaping our global economies and our future. The notion that change is the only constant holds true especially in the wake of our fast paced, innovative and increasingly digitalized economy.

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The perpetual journey of innovation - Enterprise Innovation

Engineering Humans – San Francisco State University

RACHEL'S ENVIRONMENT & HEALTH NEWS #720 ---March 15, 2001---

ENGINEERING HUMANS, PART 1 by Rachel Massey*

As we saw in our series on genetic engineering of food crops, genetic "engineers" are now moving genes around among plants, animals, and bacteria on a regular basis, but with very little understanding of the possible consequences, and almost no safety testing. Now genetic engineers are starting to modify the genes of humans, using three approaches: 1) cloning, 2) somatic cell manipulation, and 3) human germline manipulation.

Cloning: Cloning uses the DNA of an existing individual to create a new individual. The best-known example is Dolly, a sheep that was cloned using DNA from a sheep that had been dead for six years. A human has not yet been cloned, but a team of researchers including an American and an Italian recently announced they are going to attempt it.[1]

Somatic cell manipulation: Somatic cells are all the cells of the body that do not pass DNA on to the next generation. Somatic cell manipulation is currently practiced in some medical research centers under the name "gene therapy." For example, researchers are experimenting with ways to introduce genes into the blood cells of patients with hemophilia (a blood disorder), and into cells of the immune system in patients with Severe Combined Immune Deficiency (SCID), a rare inherited disorder of the immune system. The idea is to "correct" the genetic component of the disease instead of, or in addition to, treating the disease with drugs. Hundreds of trials have been carried out, but in most cases the patients have not been cured.[2]

Germline manipulation: Germ cells (sperm and eggs) do pass DNA from one generation to the next. Germline manipulation refers to changes in the germ cells changes which will be inherited by successive generations. Designing future generations through germline manipulation is still in the realm of science fiction, but just barely: some influential scientists are arguing that it should be attempted.

Why are scientists pursuing these techniques? Some researchers see somatic cell manipulation as a promising way to treat serious diseases, such as cystic fibrosis. Other genetic engineers may have less idealistic motives. Engineering human cells is technically appealing, and the mere fact that we possess this technology is, for some people, sufficient reason to use it. Some technological optimists are fascinated by the idea of germline engineering as a way to "take evolution into our own hands" by redesigning the genetic information in our children's cells.

Engineering human cells could also be a big money-maker. For example, one company hopes to create a market in "organ repair" generating cloned cells and tissues to insert into existing people's organs.[3, pg. 18] Other companies and researchers simply want to keep open the option to engineer human cells because it could be profitable in the future, even if they have not made investments in doing it right now.[3]

Cloning

There are two main applications of cloning. One is "embryo cloning," which could be used to create new human parts. For example, some scientists are working on methods to produce a new embryo from an existing person's cells and then use the cells from that embryo to produce replacements for failing body parts in the original person.[4] An embryo develops about a week after conception, and in its early stages consists of a few identical cells.

"Reproductive cloning" would produce complete cloned individuals, like Dolly the sheep. Genetic engineers are now able to clone mice and cattle as well as sheep.[5, pg. 45] Human cloning would produce a new person who is a near genetic copy of another person. He or she would, however, be different from the original person because he or she would develop in a different environment and have different experiences.

Many people think both "reproductive cloning" and "embryo cloning" are repugnant and unethical. Other people think embryo cloning could be acceptable in some cases to treat disease but think reproductive cloning is wholly unnecessary and never justifiable.

In the U.S., federal funds cannot be used for reproductive cloning experiments and some states have outlawed it, but there is no federal law against it.[5, pg. 4] A team of researchers recently announced they are going to attempt human cloning in an "unidentified Mediterranean country."[1] These researchers have been widely condemned, but some of their colleagues are primarily concerned that this early attempt at cloning could give the technology a bad name and reduce the public's willingness to allow further cloning research.

Somatic cell manipulation

Somatic cell manipulation adds genes to existing cells in some part of the human body, such as the lungs or the blood. Somatic cell manipulation is only supposed to affect the DNA of the person undergoing the treatment. In theory, it does not produce changes that could be passed on to that person's children and grandchildren.

Somatic cell manipulation was first attempted on humans in 1990.[6, pg. 110] The mechanisms of somatic cell manipulation are poorly understood, and the effects can be lethal. In one case, a teenager died after researchers at the University of Pennsylvania tried to introduce genes into his liver cells, using a modified virus to carry the genes to their destination. The idea was that the virus would "infect" the target cells and insert the desired genes, without being dangerous itself. The researchers are still not certain how they killed their patient, but evidence suggests the virus invaded many organs besides the liver and triggered a severe immune reaction.[7]

According to the U.S. Food and Drug Administration (FDA), somatic cell manipulation also poses the threat of insertional mutagenesis, in which inserting new DNA changes or disrupts the functioning of existing DNA. (See REHN #716. ) FDA also says researchers attempting to alter somatic cells could inadvertently introduce foreign genes into the patient's sperm or egg cells.[8, pg. 4689] If this happened, researchers could accidentally change the genetic information passed from parent to child.

Researchers are required to submit data to FDA and the National Institutes of Health (NIH) on any adverse effects that occur during somatic cell manipulation trials. After the teenager's death at the University of Pennsylvania, an investigation revealed that many researchers were not reporting adverse effects to NIH, which can make the information public. Some researchers say it would "confuse people" to report every death that occurs during these trials because many participants are seriously ill and could die for reasons unrelated to the treatment.[9]

Right now, most information that researchers submit to FDA on somatic cell manipulation experiments is kept secret.[8, pg. 4688] The agency has issued proposed regulations under which information about somatic cell manipulation trials will be made available to the public, and is accepting comments on the proposed regulations until April 18, 2001.[10]

Germline manipulation

Germline manipulation permanently changes the inheritable characteristics passed from one generation to the next. This can be done by altering sperm or egg cells or by altering an embryo. If an engineered embryo survives and develops into a baby, the changes introduced by germline manipulation will be present in every cell of that baby. If the baby survives to adulthood and has children, the changes will be passed on to future generations, through that person's sperm or egg cells.

Some researchers try to justify germline manipulation by saying it could remove or replace DNA associated with an inherited disease. This is a far-fetched idea and unnecessary; even if both members of a couple have the genes for a hereditary disease, there are other ways to produce a child without the disease, including using donated sperm or eggs. Other researchers say they want to
use germline engineering to give a baby new genetic features it could not have gotten from its parents. This goal cannot be achieved through any other technology. It is also a goal that, by definition, could never be medically necessary because it would not serve to relieve sickness in an existing person. Instead, it would aim to "improve" future generations of human beings.[6, pg. 113]

The attempt to "improve" the human race genetically -- as one might create a specialized breed of horses or dogs -- is known as eugenics. In the early decades of the 20th century, eugenics projects in the U.S. led to forced sterilization of some people who were considered to have undesirable traits. This included prison inmates who were considered to be "hereditary criminals." One forced sterilization was justified by describing a man as "subnormal mentally," with "every appearance and indication of immorality."[6, pgs. 20-21] In Nazi Germany, the systematic extermination of Jews and other people was one part of a eugenic project to breed a "superior race."[6, pg. 17]

Some prominent scientists hope to achieve eugenic goals through genetic engineering instead of through breeding. Molecular biologist Daniel Koshland, formerly the editor of SCIENCE magazine, argues that "if a child destined to have a permanently low IQ could be cured by replacing a gene, would anyone really argue against that?" He continues, "It is a short step from that decision to improving a normal IQ. Is there an argument against making superior individuals?... As society gets more complex, perhaps it must select for individuals more capable of coping with its complex problems."[4, pgs. 115-116]

To be continued.

==============

*Rachel Massey is a consultant to Environmental Research Foundation.

[1] Jane Barrett, "U.S., Italian Experts Plan to Clone Humans," Reuters (March 9, 2001). Available at http://dailynews.yahoo.- com/ htx/nm/20010309/sc/italy_cloning_dc_2.html

[2] Larry Thompson, "Human Gene Therapy: Harsh Lessons, High Hopes," FDA CONSUMER MAGAZINE (September-October 2000) Available at http://www.fda.gov/fdac/features/2000/500_gene.html

[3] See Sarah Sexton, "If Cloning is the Answer, What was the Question?: Power and Decision-Making in the Geneticisation of Health," THE CORNERHOUSE Briefing 16 (1999). Available at http://cornerhouse.icaap.org/briefings/16.html

[4] Emma Young, "Stem Cell Go-Ahead," NEW SCIENTIST ONLINE (December 20, 2000). Available at http://www.newscientist.com- /nsplus/insight/clone/stem/goahead.html.

[5] Margaret Talbot, "The Cloning Mission: A Desire to Duplicate," NEW YORK TIMES MAGAZINE (February 4, 2001), pgs. 40-45, 67-68.

[6] Ruth Hubbard and Elijah Wald, EXPLODING THE GENE MYTH: HOW GENETIC INFORMATION IS PRODUCED AND MANIPULATED BY SCIENTISTS, PHYSICIANS, EMPLOYERS, INSURANCE COMPANIES, EDUCATORS, AND LAW ENFORCERS [ISBN 0807004316]. (Boston: Beacon Press, 1999).

[7] Eliot Marshall, "Gene Therapy Death Prompts Review of Adenovirus Vector," SCIENCE Vol. 286, No. 5448 (December 17, 1999), pgs. 2244-2245.

[8] Food and Drug Administration, "Availability for Public Disclosure and Submission to FDA for Public Disclosure of Certain Data and Information Related to Human Gene Therapy or Xeno- transplantation," FEDERAL REGISTER Vol. 66, No. 12 (January 18, 2001), pgs. 4688-4706. Available at http://frwebgate.access.gpo.- gov/cgi-bin/getdoc.cgi?dbname=2001_register&docid=01-1048-fild

[9] Maggie Fox, "Gene Therapy Under Fire," Reuters (January 31, 2000). Available at http://www.abcnews.go.com/sections/living/- DailyNews/genetherapy_000130.html

[10] See Council for Responsible Genetics Alert, "Tell the FDA that the Public has a Right to Know about Xenotransplantation and Gene Therapy, February 28, 2001." Available at http://www.gene-watch.org/crgalerts.html

. . RACHEL'S ENVIRONMENT & HEALTH NEWS #721 . . ---March 29, 2001--- . . HEADLINES: . . ENGINEERING HUMANS, PART 2 . . ========== . . ENGINEERING HUMANS, PART 2

Human beings can be genetically engineered in three ways: by inserting genes into the cells of existing people (somatic cell manipulation, sometimes called "gene therapy"); by trying to copy an existing person (cloning); or by changing the genes of future generations (germline manipulation). Here we will examine serious proposals to modify the human germline to "improve" the human species, or perhaps even to create an entirely new species of humans. Researchers have not yet tried to manipulate the human germline, but proponents would like to convince us all that its a good idea.

Biologist Daniel Koshland of the University of California at Berkeley, a former editor of SCIENCE magazine, is a leading advocate of genetic engineering to improve the human species. Koshland writes, "If we do go ahead with germline engineering, as I think we should, I can't see any possible reason for not allowing enhancement therapy. We are facing monumental problems with the population explosion, environmental pollution, the shortage of fossil fuels, and the serious lack of leadership.... Should we turn our back on new methodologies that might bring us smarter people and better leaders who are more responsible in their lives? It's going to be tricky, but it seems silly to shut our eyes to a new technology like this."[1, pg. 29]

In other words, Koshland is urging us to solve social and environmental problems by redesigning our children. Unfortunately, there is zero evidence that gene manipulation can instill "leadership" or "responsibility" in babies. As for making people smarter, even if it were possible there is no reason to think "smarter" people are the solution to humanity's problems. Many of the problems we face were created by some of the smartest people in the world -- and were then loosed upon the world with little consideration of the consequences.

The problems of technology and leadership today can both be traced to a common source: decisions made by elites who don't engage the people affected by their decisions. What we need is not "smarter" people groomed to impose decisions on the rest of us, as happens now; instead, we need more people with common sense participating in decisions. In other words, we need to make decisions in new ways, with the democratic participation of everyone who will be affected.[2]

Some of Koshland's colleagues paint an even more extreme picture of what genetic engineering could mean for the human race. Lee Silver, a molecular biologist at Princeton University, writes about future scenarios in which parents could design embryos to suit their preferences. He suggests the human race could eventually divide into two species, one with a normal set of genes and the other with various expensive genetic "improvements." The new race of improved humans might be unable to mate with ordinary humans due to genetic incompatibility, Silver says.[3] In the future that Silver envisions, the divide between rich and poor would be permanently coded into our cells, much as Aldous Huxley foretold in BRAVE NEW WORLD in 1932.

W. French Anderson of the University of Southern California School of Medicine wants to try engineering the somatic cells of fetuses as they develop in the womb. Anderson hopes this might be a way to "cure" inherited diseases;[4] other researchers even hope to get rid of unwanted traits such as high cholesterol levels.[5] Almost all attempts to cure disease in adults or children through somatic cell manipulation have failed, but some proponents say a consistent record of failure is no reason to delay experiments on fetuses.[6]

Anderson and others say they plan to leave the future sperm or egg cells of a fetus intact, but they acknowledge they could alter sperm and eggs by accident, thus producing changes that could be inherited by future generations.[4]

It seems unlikely that any of this will ever succeed. Genes usually do not control just one characteristic, so changing a gene is likely to have multiple consequences. Furthermore, a single characteri
stic may be controlled by several genes. These facts make it seem unlikely that gene therapy or germline engineering of humans will ever produce the desired results without creating new problems.

Researchers recently introduced a gene for a fluorescent (glowing) protein into the cells of fourteen fetal monkeys,[7] but the monkeys' cells stopped producing the fluorescent protein a few months after birth; evidently, they shut off the foreign genes as they matured.[7, pg. 134]

We know from plant experiments that foreign genes often behave unpredictably. In one case, petunias were engineered to produce salmon-red flowers. When the weather turned unusually hot, the engineered petunias began producing flowers of other colors. Apparently the stress of high temperatures caused the plants, unpredictably, to shut down some of the foreign genes.[8] If monkeys shut off foreign genes as they mature, and if plants shut down foreign genes in response to stress, should we expect foreign genes in humans to behave differently?

When researchers genetically manipulate any plant or animal -- whether they are making clones or adding genes to existing embryos -- they routinely produce organisms that are abnormal in disastrous ways. It can take thousands of tries before genetic engineers get the results they want in an engineered plant, and many engineered plants are discarded because they are deformed or display an unintended new feature.[9, pg. 3] When researchers clone animals or manipulate the cells of animal embryos, the resulting creatures often have severe defects.[10]

Germline engineering in animals, as in plants, can lead to insertional mutation a change in gene function caused by a foreign gene inserted into the middle of an existing gene. (See REHN #716.) In one case, scientists created several generations of mice with deformities resulting from an insertional mutation.[11] If researchers introduced an insertional mutation into a human embryo, they would create a baby with a defect that could become obvious at birth, later in life, or only when the victim of the experiment grew up and had children.

In general, problems that have arisen in genetic engineering experiments on plants and animals can be expected to appear in experiments on humans. But theres an important difference: Genetic engineers who work with plants or rodents can breed multiple generations to test whether an inserted gene performs as expected in a laboratory setting. With humans, we cannot breed test generations in a lab.

Some people still argue that somatic cell manipulation on consenting individuals could be justified to treat serious disease, if it could ever be shown to work the way it is supposed to. Germline manipulation, in contrast, can never be justified as a medical treatment, unless we redefine medicine to include "curing" people who have not yet been conceived. For this and other reasons, many people consider germline manipulation wholly unacceptable. Altering the genes of future generations would amount to a dangerous experiment carried out on subjects who have no choice about participating. The United Nations' International Covenant on Civil and Political Rights, which the U.S. ratified in 1992, prohibits medical or scientific experimentation on individuals who have not consented freely to participate.[12]

Whether they want to insert foreign genes into adult cells, "enhance" an embryo, or redesign a fetus, proponents of human engineering often talk as though genes were the key to controlling health and disease. In fact, few diseases are strictly determined by genes. In the vast majority of cases, disease is produced or prevented through interactions between genes and our social and physical environments.[13] For example, certain genetic mutations may increase the likelihood of breast cancer, but women with these mutations will not necessarily develop breast cancer. Furthermore, 90% of women who do develop breast cancer do not have a family history of the disease and therefore probably did not develop it because of a gene.[14, pgs. 168-170]

Focusing on the genetic elements of sickness and health diverts attention away from the social and environmental causes of disease and makes it easy to blame preventable illnesses on "bad genes." If our goal is healthier, smarter, or otherwise "improved" future generations, there are obvious ways to achieve that goal, such as protecting pregnant women and their babies from toxic exposures and making sure all women have opportunities for good nutrition and health care during pregnancy.

To learn more or to join the effort to prevent dangerous and unethical genetic engineering of humans, contact:

** Exploratory Initiative on the New Human Genetic Technologies (San Francisco, Calif.): (415) 434-1403; E-mail: humanfuture@publicmediacenter.org. To sign up for the Exploratory Initiative's E-mail newsletter, GENETIC CROSSROADS , or to request a free briefing packet on human cloning and genetic manipulation, send E-mail to teel@adax.com.

** Council for Responsible Genetics (Cambridge, Mass.): (617) 868-0870; E-mail crg@gene-watch.org; web: http://- http://www.gene-watch.org

** Human Genetics Alert: web: http://www.- users.globalnet.co.uk/~cahg/ --Rachel Massey and Peter Montague

==============

[1] Gregory Stock and John Campbell, editors, ENGINEERING THE HUMAN GERMLINE: AN EXPLORATION OF THE SCIENCE AND ETHICS OF ALTERING THE GENES WE PASS TO OUR CHILDREN [ISBN 0195133021] (N.Y.: Oxford University Press, 2000), pgs. 29, 67-71.

[2] See, for example, Benjamin R. Barber, STRONG DEMOCRACY: PARTICIPATORY POLITICS FOR A NEW AGE [ISBN 0520056167] (Berkeley, Calif.: University of California Press, 1984).

[3] Lee M. Silver, REMAKING EDEN: HOW GENETIC ENGINEERING AND CLONING WILL TRANSFORM THE AMERICAN FAMILY [ISBN 0380792435] (N.Y.: Avon Books, 1998).

[4] Jennifer Couzin, "RAC Confronts in Utero Gene Therapy Proposals," SCIENCE Vol. 282, No. 5386 (October 2, 1998), pg. 27.

[5] Joanna Marchant, "Generation Game," NEW SCIENTIST Vol. 168, no. 2267 (December 2, 2000) pgs. 16-17.

[6] Holm Schneider and Charles Coutelle, "In Utero Gene Therapy: The Case For," NATURE MEDICINE Vol. 5, No. 3 (March 1999), pgs. 256-257.

[7] Alice F. Tarantal and others, "Rhesus Monkey Model for Fetal Gene Transfer: Studies with Retroviral-Based Vector Systems," MOLECULAR THERAPY Vol. 3, No. 2 (February 2001), pgs. 128-138

[8] Peter Meyer and others, "Endogenous and environmental factors influence 35S promoter methylation of a maize A1 gene construct in transgenic petunia and its colour phenotype," MOLECULAR GENES AND GENETICS Vol. 231, no. 3 (Febr. 1992), pgs. 345-352.

[9] Michael K. Hansen, "Genetic Engineering is Not an Extension of Conventional Plant Breeding; How Genetic Engineering Differs from Conventional Breeding, Hybridization, Wide Crosses and Horizontal Gene Transfer," report produced by Consumers Union. Available at http://www.consumersunion.org/food/widecpi200.htm.

[10] Rudolf Jaenisch and Ian Wilmut, "Don't Clone Humans," SCIENCE Vol. 291, No. 5513 (March 30, 2001), pg. 2552. Also see Lorraine E. Young and others, "Large Offspring Syndrome in Cattle and Sheep," REVIEWS OF REPRODUCTION Vol. 3 (September 3, 1998), pgs. 155-163.

[11] Chao-Nan Ting and others, "Insertional Mutation on Mouse Chromosome 18 with Vestibular and Craniofacial Abnormalities," GENETICS Vol. 136, No. 1 (January 1994), pgs. 247-254.

[12] United Nations High Commission for Human Rights, INTERNATIONAL COVENANT ON CIVIL AND POLITICAL RIGHTS (December 16, 1966). Available at http://www.unhchr.ch/html/menu3/b/a_ccpr.htm

[13] David E. Larson, editor, MAYO CLINIC FAMILY HEALTH BOOK [ISBN 0688144780], 2nd Edition (N.Y.: William Morrow, 1996), pg. 42.

[14] Ruth Hubbard and Elijah Wald, EXPLODING THE GENE MYTH: HOW GENETIC INFORMATION IS PRODUCED AND MANIPULATED BY SCIENTISTS, PHYSICIANS, EMPLOYERS, INSURANCE COMPANIES, EDUCATORS, AND LAW ENFORCERS [ISBN 0807004312] (Boston: Beacon Press, 1999). < /p>

Thanks to Marcy Darnovsky of the Exploratory Initiative on the New Human Genetic Technologies for reviewing portions of this series.

################################################################ NOTICE In accordance with Title 17 U.S.C. Section 107 this material is distributed without profit to those who have expressed a prior interest in receiving it for research and educational purposes. Environmental Research Foundation provides this electronic version of RACHEL'S ENVIRONMENT & HEALTH WEEKLY free of charge even though it costs the organization considerable time and money to produce it. We would like to continue to provide this service free. You could help by making a tax-deductible contribution (anything you can afford, whether $5.00 or $500.00). Please send your tax-deductible contribution to: Environmental Research Foundation, P.O. Box 5036, Annapolis, MD 21403-7036. Please do not send credit card information via E-mail. For further information about making tax-deductible contributions to E.R.F. by credit card please phone us toll free at 1-888-2RACHEL, or at (410) 263-1584, or fax us at (410) 263-8944. --Peter Montague, Editor ################################################################

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Engineering Humans - San Francisco State University

Bioethics Of Human Genetic Engineering – Documentary Video …

In Vivo : Selected Stories of Genetic Engineering (1996)- Robert Wyrod This experimental documentary examines the frontiers of human genetic engineering. It explores the ethical terrain of the e... | more... In Vivo : Selected Stories of Genetic Engineering (1996)- Robert Wyrod This experimental documentary examines the frontiers of human genetic engineering. It explores the ethical terrain of the emerging field of human gene therapy research and includes original interviews with the leading scientists working in this area. Director: Robert Wyrod Producer: Robert Wyrod Keywords: genetic; engineering; gene therapy; DNA; experimental; clone; molecular Contact Information: robertwyrod@gmail.com Creative Commons license: Attribution-Noncommercial 3.0 Human genetic engineering is the genetic engineering of humans by modifying the genotype of the unborn individual to control what traits it will possess when born.[1] Humans do not need gene therapy to survive, though it may prove helpful to treat certain diseases. Special gene modification research has been carried out on groups such as the 'bubble children' - those whose immune systems do not protect them from the bacteria and irritants all around them. The first clinical trial of human gene therapy began in 1990, but (as of 2008) is still experimental. Other forms of human genetic engineering are still theoretical, or restricted to fiction stories. Recombinant DNA research is usually performed to study gene expression and various human diseases. Some drastic demonstrations of gene modification have been made with mice and other animals, however; testing on humans is generally considered off-limits. In some instances changes are usually brought about by removing genetic material from one organism and transferring them into another species. There are two main types of genetic engineering. Somatic modifications involve adding genes to cells other than egg or sperm cells. For example, if a person had a disease caused by a defective gene, a healthy gene could be added to the affected cells to treat the disorder. The distinguishing characteristic of somatic engineering is that it is non-inheritable, e.g. the new gene would not be passed to the recipients offspring. Germline engineering would change genes in eggs, sperm, or very early embryos. This type of engineering is inheritable, meaning that the modified genes would appear not only in any children that resulted from the procedure, but in all succeeding generations. This application is by far the more consequential as it could open the door to the perpetual and irreversible alteration of the human species. There are two techniques researchers are currently experimenting with: Viruses are good at injecting their DNA payload into human cells and reproducing it. By adding the desired DNA to the DNA of non-pathogenic virus, a small amount of virus will reproduce the desired DNA and spread it all over the body. Manufacture large quantities of DNA, and somehow package it to induce the target cells to accept it, either as an addition to one of the original 23 chromosomes, or as an independent 24th human artificial chromosome. Human genetic engineering means that some part of the genes or DNA of a person are changed. It is possible that through engineering, people could be given more arms, bigger brains or other structural alterations if desired. A more common type of change would be finding the genes of extraordinary people, such as those for intelligence, stamina, longevity, and incorporating those in embryos. Human genetic engineering holds the promise of being able to cure diseases and increasing the immunity of people to viruses. An example of such a disease is cystic fibrosis, a genetic disease that affects lungs and other organs. Researchers are currently trying to map out and assign genes to different body functions or disease. When the genes or DNA sequence responsible for a disease is found, theoretically gene therapy should be able to fix the disease and eliminate it permanently. However, with the complexity of interaction between genes and gene triggers, gene research is currently in its infancy. Computer modeling and expression technology could be used in the future to create people from scratch. This would work by taking existing DNA knowledge and inserting DNA of "superior" body expressions from people, such as a bigger heart, stronger muscles, etc and implanting this within an egg to be inserted into a female womb. The visual modeling of this process may be very much like the videogame Spore, where people are able to manipulate the physical attributes of creatures and then "release them" in the digital world. | less...

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Human Genetics Alert – Human Genetic Engineering resources

1. Is human genetic engineering safe and effective?

With present techniques it is clearly unsafe: the techniques of inserting genes can disrupt other genes, with harmful consequences for the person and all his/her descendants. We do not know enough about how gene work to ensure that an inserted gene will work as desired. Future generations cannot consent to such risks. The chance that interventions will be effective is unknown. However, the technologies are improving constantly and may make human genetic engineering (HGE) feasible within five years.

No, it is not. Advocates argue that it is a general solution to the problem of genetic diseases and is superior to somatic gene therapy, since it could permanently eliminate the risk of inherited disease within a family. However, there are only a few very rare cases where HGE is the only option for producing a healthy child. Couples can choose not to have children, to adopt a child, or to use donor eggs or sperm. If it is consistent with their values, they can also use prenatal and pre-implantation genetic testing to avoid genetic disease and have a child that is 100% genetically related. Given this, it is clear that the real market for HGE is in 'enhancement' of appearance, height, athletic ability, intelligence, etc.

No, it is not, although Lee Silver and others like him very much want you to believe that it is. In a democratic society people agree on what rules they wish to live under. By 1998 twenty-seven industrial democracies had agreed to ban human cloning and germ line manipulation. In the U.S., the state of Michigan has made all forms of human cloning illegal. There is no reason we cannot choose to forgo these technologies, both domestically and as part of a global compact. It is often said that banning the use of a technology will not prevent someone from developing it elsewhere. This may be true, although the number of people competent to develop cloning and human genetic engineering is small. But even though the technology may be developed, we do not have to permit its use to become respectable and widespread.

No, we have the right to choose the science that we want and to define our own vision of progress. We should reject science which is not in the public interest. Proscribing the most dangerous techno-eugenic applications will allow us to proceed with greater confidence in developing the many potentially beneficial uses of genetic research for human society.

People do have the right to have children if they are biologically capable, but they do not have any 'right' to use cloning, or genetic engineering. Rights don't exist in a vacuum; they are socially negotiated within a context of fundamental values. The question of access to particular technologies is a matter of public policy and depends on the social consequences of allowing that access. For example, people are not allowed access to nuclear technology, or dangerous pathogens and drugs, simply because they have the money to pay for them.

Traditionally, we see human beings as inviolable, and as endowed with rights: they must be accepted as they are. Human genetic engineering overthrows that basic conception, degrading human subjects into objects, to be designed according parents' whim. Accepting such a change would have consequences both for individual humans and for society at large which we can barely imagine. Obvious consequences would be a disruption of parents' unconditional love for children. Cloning and HGE represent an unprecedented intent to determine and control a child's life trajectory: for the child, it would undermine their sense of free will and of their achievements. These concerns are what many people mean when they say that we should not play God with our children.

The social consequences of the use of cloning and HGE in our society would be disastrous. Parents would tend to engineer children to conform to social norms, with regard to physical ability, appearance and aptitudes, even though many of those social norms are inherently oppressive. For example, disabled people have often expressed fears that free-market eugenics would reduce society's tolerance for those genetic impairments. If genes pre-disposing people to homosexuality are discovered, it is certain that many people would attempt to engineer these out of their offspring. A free-market techno-eugenics could also easily have the disastrous consequences spelled out in Lee Silver's Re-making Eden. Since access to such expensive technology would be on the basis of ability to pay, we could see the emergence of biologically as well as financially advantaged ruling elites.

The environmental movement has recognised how, in Western societies over the last few hundred years, humans have tried to control and dominate nature, with the resultant environmental crisis which we currently face. Genetic engineering of plants and animals gives us the power to dominate nature in a new and more powerful way than ever before, which is why it has caused so much concern in environmental movements. Techno-eugenics extends the drive to control nature to the nature of human beings, threatening ultimately to make the human species, like other species, the object of the manipulative control of technocratic elites. It is obvious that if we cannot prevent this, we have little chance of winning the struggle to protect the environment. The environmental movement is the main guardian of the non-exploitative vision of the relation between humans and the rest of nature. Realising that such a relationship may soon be imposed upon ourselves, and our children, the environmental movement must take the lead in alerting society to the danger that it faces.

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Human Genetics Alert - Human Genetic Engineering resources

Genetic Engineering In Humans

Human genetic engineering is one of the most controversial aspects of a science, which is itself highly controversial, and it is still very much in its infancy. There have been a few isolated cases where an illness has been successfully cured by the use of genetic therapy, but there have also been other cases where patients have contracted diseases such as leukemia through experimentation with this type of therapy. At this stage it is impossible to say exactly what the future will hold, or exactly what the consequences of these developments will be.

So far, the only successes which the method has are in treating conditions relating to the human immune system. This is an obvious application of the technology, as the condition is caused purely by genetic factors. By replacing a gene which gives the patient a proclivity towards the disease with a healthy one a cure can be effected. This is more than just theory, as the numbers of cases where this has been successfully carried out is now into double figures, and is constantly increasing. The challenge lies in overcoming the potentially catastrophic side effects which can occur if the treatment does not work.

One of the most controversial of all applications of this technology is in allowing infertile mothers to conceive. This is done by using the eggs from a different mother, leaving the child with the genetic blueprint inherited from three people. This will then be passed on through future generations, leading to untold potential complications. It is still far too early to judge the potential consequences of the use of this type of genetic technology, but if there are any negative side effects they are likely to be far reaching and extremely damaging.

There have been many arguments put forward concerning human genetic engineering, some strongly in favor and some equally strongly against. The potential is there for diseases caused by genetics to be eliminated completely, and this is there area in which fewest dissenting voices will be heard. The use of genetics purely to overcome fertility is far more controversial, especially when you consider the permanent effect that this has on all future generations of that family. There are also many dissenters against the possibility of parents deciding features of their children using an advanced form of this technology, which cannot be used yet but which may be perfectly possible in the future.

If this technology is left unchecked it will definitely have far reaching consequences. There is no doubt that wealthy families would take advantage of such technology to try to give their children every advantage in their future life, and there could be several possible outcomes of this. One would be a rise in productivity and creativity which would penetrate through society, raising the standard of society for everyone and creating more opportunities. It is also possible that poor families who could not afford this technology would be left even further adrift, leading to sharp increases in crime rates, social disorder, and economic chaos.

Even though strong opinions are held on both sides of the argument, the truth is that it is far too early to know for sure exactly what is involved with human genetic engineering. There are some philosophical and moral arguments which will prove exceedingly difficult to resolve one way or another, but there are potential consequences which cannot possibly be known until more research has been carried out. The arguments over this technology are certain to rage for a great many years to come, and it is unlikely there will ever be universal agreement on human genetic engineering.

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Genetic Engineering In Humans

Online Debate: Human genetic engineering is a good thing …

My argument is that genetic engineering, and specifically human genetic engineering is a good thing.

I believe that human genetic engineering (HGE) can benefit human kind in an endless number of ways including but not limited to :

*Increased lifespan *Decreasing disease *Making humans happier *Making humans stronger *Making humans smarter *Making humans better looking (Yes, even this can be done and is good)

I will let my opponent make the first actual argument and I will then, after my opponent has made their argument, go into much further detail on my own argument as well as addressing theirs. So, I leave it to any challenger to argue against my initial statements and my general argument.

Con, I await your response. 🙂

Increased lifespan-If HGE did increase human lifespan why would us as a society want that? Thousands of people are brain dead and have you ever heard of this? http://en.wikipedia.org...

Making humans happier-I know many kids who are made fun of for being gay,black, Mormon etc.So if I was a clone (or altered) I am certain I would be made fun of way more than anyone else.Also kids have trouble when they are adopted, and can not find their family.If I was a clone, and I didn't even have a family?I would have no real family and thus no reason to be happy.

Better looking- hhttp://gorillasafariadventure.com... http://alpha-mag.blogspot.com... One is real......

At first, since as everything is economic, the rich people would be the first to try and use HGH (as they use HRT today more commonly). How would we know it works? We would know that it would work through scientific testing, lab testing, finally human testing. Etc. It would be a long process. Eventually everyone would be able to afford it as technology improves.

The upper class having exclusive rights to these technologies would last a few decades at most. Perhaps less.

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Online Debate: Human genetic engineering is a good thing ...

Human Genetics Alert – The Threat of Human Genetic Engineering

David King

The main debate around human genetics currently centres on the ethics of genetic testing, and possibilities for genetic discrimination and selective eugenics. But while ethicists and the media constantly re-hash these issues, a small group of scientists and publicists are working towards an even more frightening prospect: the intentional genetic engineering of human beings. Just as Ian Wilmut presented us with the first clone of an adult mammal, Dolly, as a fait accompli, so these scientists aim to set in place the tools of a new techno-eugenics, before the public has ever had a chance to decide whether this is the direction we want to go in. The publicists, meanwhile are trying to convince us that these developments are inevitable. The Campaign Against Human Genetic Engineering, has been set up in response to this threat.

Currently, genetic engineering is only applied to non-reproductive cells (this is known as 'gene therapy') in order to treat diseases in a single patient, rather than in all their descendants. Gene therapy is still very unsuccessful, and we are often told that the prospect of reproductive genetic engineering is remote. In fact, the basic technologies for human genetic engineering (HGE) have been available for some time and at present are being refined and improved in a number of ways. We should not make the same mistake that was made with cloning, and assume that the issue is one for the far future.

In the first instance, the likely justifications of HGE will be medical. One major step towards reproductive genetic engineering is the proposal by US gene therapy pioneer, French Anderson, to begin doing gene therapy on foetuses, to treat certain genetic diseases. Although not directly targeted at reproductive cells, Anderson's proposed technique poses a relatively high risk that genes will be 'inadvertently' altered in the reproductive cells of the foetus, as well as in the blood cells which he wants to fix. Thus, if he is allowed to go ahead, the descendants of the foetus will be genetically engineered in every cell of their body. Another scientist, James Grifo of New York University is transferring cell nuclei from the eggs of older to younger women, using similar techniques to those used in cloning. He aims to overcome certain fertility problems, but the result would be babies with three genetic parents, arguably a form of HGE. In addition to the two normal parents, these babies will have mitochondria (gene-containing subcellular bodies which control energy production in cells) from the younger woman.

Anderson is a declared advocate of HGE for medical purposes, and was a speaker at a symposium last year at UCLA, at which advocates of HGE set out their stall. At the symposium, which was attended by nearly 1,000 people, James Watson, of DNA discovery fame, advocated the use of HGE not merely for medical purposes, but for 'enhancement': 'And the other thing, because no one really has the guts to say it, I mean, if we could make better human beings by knowing how to add genes, why shouldn't we do it?'

In his recent book, Re-Making Eden (1998), Princeton biologist, Lee Silver celebrates the coming future of human 'enhancement', in which the health, appearance, personality, cognitive ability, sensory capacity, and life-span of our children all become artifacts of genetic engineering, literally selected from a catalog. Silver acknowledges that the costs of these technologies will limit their full use to only a small 'elite', so that over time society will segregate into the "GenRich" and the "Naturals":

"The GenRich - who account for 10 percent of the American population - all carry synthetic genes... that were created in the laboratory ...All aspects of the economy, the media, the entertainment industry, and the knowledge industry are controlled by members of the GenRich class...Naturals work as low-paid service providers or as labourers, and their children go to public schools... If the accumulation of genetic knowledge and advances in genetic enhancement technology continue ... the GenRich class and the Natural class will become...entirely separate species with no ability to cross-breed, and with as much romantic interest in each other as a current human would have for a chimpanzee."

Silver, another speaker at the UCLA symposium, believes that these trends should not and cannot be stopped, because to do so would infringe on liberty.

Most scientists say that what is preventing them from embarking on HGE is the risk that the process will itself generate new mutations, which will be passed on to future generations. Official scientific and ethical bodies tend to rely on this as the basis for forbidding attempts at HGE, rather than any principled opposition to the idea.

In my view, we should not allow ourselves to be lulled into a false sense of security by this argument. Experience with genetically engineered crops, for example, shows that we are unlikely ever to arrive at a situation when we can be sure that the risks are zero. Instead, when scientists are ready to proceed, we will be told that the risks are 'acceptable', compared to the benefits. Meanwhile, there will be people telling us loudly that since they are taking the risks with their children, we have no right to interfere.

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Human Genetics Alert - The Threat of Human Genetic Engineering

Human Genetic Engineering Cons: Why This Branch of Science …

A Slippery Slope? Ethics of Human Genetic Engineering

To say that genetic engineering has attracted some controversy would be an understatement. There are many cries that scientists are 'playing God' and that it will lead to a two-tier society - the genetically haves and the have-nots. But is this any different to the cries of horror and fears of Frankenstein's monster that greeted Louise Brown, the first child to be born by IVF treatment? There was great uproar in the late 1970's but IVF is now a common, if expensive, fertility treatment. And there aren't any monsters stalking the Earth.

Having said that, genetic engineering does hold the potential that parents could (if the technology worked) assemble their kids genetically, to be smarter, to be more athletic or have a particular hair or eye colour. Though it's rather fanciful to suggest that intelligence could be improved by the substitution of a gene, it may be found that there are several genes that are more commonly expressed in the genomes of intelligent people than those with more limited intellectual capacity. And parents might want to engineer an embryo to house a greater number of these genes. It is this genetic engineering of humans that so frightens people, that we could somehow design the human race. Though some people point out other potential benefits. What if it turned out that there were sets of genes that were commonly expressed in criminals - could we tackle crime by weeding out those genes?

The technology is nowhere near there yet, but a tiny number of parents undergoing IVF have selected their embryos to be free from genetic mutations that have blighted generations of their family. In the UK in January 2009 a mother gave birth to a girl whose embryo had been selected to be free from a genetic form of breast cancer. Some see this as a slippery slope towards a eugenic future, others view it as a valuable use of genetic engineering to prevent disease from striking someone down.

Society will decide how it uses this technology, and it is for governments to weigh up the pros and cons of genetic engineering in humans to see what may be carried out and what should be illegal. They will be prompted by public understanding, desire and concern. It therefore behoves all of us to understand what scientists are trying to accomplish and what they are not trying to do. We must all become better informed, to equip ourselves with more information and to know the difference between science fiction and science fact.

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Human Genetic Engineering Cons: Why This Branch of Science ...