Category Archives: Human Genetic Engineering

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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Bioethics Of Human Genetic Engineering - Documentary Video ...

The human body is not perfect. Some are created with inherent faults and others break down before their time. Science has the potential to make good these problems by altering how humans are made. This is genetic engineering, and this article looks at the pros and cons of the technology in humans

This is part one of a two-part series. Here I will look at a definition of genetic engineering and the pros of human genetic engineering. In part two the cons and the ethics of human genetic engineering are discussed.

Before weighing up the pros and cons of genetic engineering in humans, it's worth taking the time to understand just what is meant by the idea. Simply put, it's a way of manipulating our genes in such a way as to make our bodies better. This alteration of a genome could take place in the sperm and egg cells. This is known as germline gene therapy and would alter the traits that a child is born with. The changes would be inheritable and passed down through the generations. It is currently illegal in many countries.

The other way to change our genome is to swap our bad genes for good ones - in cells other than the sex cells. This is known as somatic cell gene therapy. This is where a functioning gene could be fired into our bodies on a viral vector to carry out the functions that a faulty gene is unable to. This technology is permitted, though it has enjoyed a very limited success rate so far (largely because it is technically very difficult). Nonetheless, it still holds out a great deal of promise.

There are many potential advantages to being able to alter the cells in our bodies genetically.

To make disease a thing of the past

Most people on the planet die of disease or have family members that do. Very few of us will just pop up to bed one night and gently close our eyes for the last time. Our genomes are not as robust as we would like them to be and genetic mutations either directly cause a disease such as Cystic fibrosis, or they contribute to it greatly i.e. Alzheimer's. Or in the case of some conditions such as the heart disease Cardiomyopathy, genetic mutations can make our bodies more susceptible to attack from viruses or our own immune system. If the full benefits of gene therapy are ever realised we can replace the dud genes with correctly functioning copies.

To extend life spans

Having enjoyed life, most of us want to cling on to it for as long as possible. The genetic engineering of humans has the potential to greatly increase our life spans. Some estimates reckon that 100-150 years could be the norm. Of course gene therapy for a fatal condition will increase the lifespan of the patient but we're also talking about genetic modifications of healthy people to give them a longer life. Once we fully understand the genetics of ageing it may be possible to slow down or reverse some of the cellular mechanisms that lead to our decline - for example by preventing telomeres at the ends of chromosomes from shortening. Telomere shortening is known to contribute to cell senescence.

Better pharmaceuticals

The knowledge gained by working out genetic solutions for the above could help with the design of better pharmaceutical products that are able to target specifically genetic mutations in each individual.

So What's the Downside?

As deliriously exciting as some people believe genetic engineering to be - there are several downsides and ethical dilemmas. Click the link to read the cons.

This two part series explores some of the pros and cons of human genetic engineering.

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Pros and Cons of Genetic Engineering in Humans - Part 1

Photo by: Gernot Krautberger

Genetic engineering is any process by which genetic material (the building blocks of heredity) is changed in such a way as to make possible the production of new substances or new functions. As an example, biologists have now learned how to transplant the gene that produces light in a firefly into tobacco plants. The function of that genethe production of lighthas been added to the normal list of functions of the tobacco plants.

Genetic engineering became possible only when scientists had discovered exactly what is a gene. Prior to the 1950s, the term gene was used to stand for a unit by which some genetic characteristic was transmitted from one generation to the next. Biologists talked about a "gene" for hair color, although they really had no idea as to what that gene was or what it looked like.

That situation changed dramatically in 1953. The English chemist Francis Crick (1916 ) and the American biologist James Watson (1928 ) determined a chemical explanation for a gene. Crick and Watson discovered the chemical structure for large, complex molecules that occur in the nuclei of all living cells, known as deoxyribonucleic acid (DNA).

DNA molecules, Crick and Watson announced, are very long chains or units made of a combination of a simple sugar and a phosphate group.

Amino acid: An organic compound from which proteins are made.

DNA (deoxyribonucleic acid): A large, complex chemical compound that makes up the core of a chromosome and whose segments consist of genes.

Gene: A segment of a DNA molecule that acts as a kind of code for the production of some specific protein. Genes carry instructions for the formation, functioning, and transmission of specific traits from one generation to another.

Gene splicing: The process by which genes are cut apart and put back together to provide them with some new function.

Genetic code: A set of nitrogen base combinations that act as a code for the production of certain amino acids.

Host cell: The cell into which a new gene is transplanted in genetic engineering.

Human gene therapy (HGT): The application of genetic engineering technology for the cure of genetic disorders.

Nitrogen base: An organic compound consisting of carbon, hydrogen, oxygen, and nitrogen arranged in a ring that plays an essential role in the structure of DNA molecules.

Plasmid: A circular form of DNA often used as a vector in genetic engineering.

Protein: Large molecules that are essential to the structure and functioning of all living cells.

Recombinant DNA research (rDNA research): Genetic engineering; a technique for adding new instructions to the DNA of a host cell by combining genes from two different sources.

Vector: An organism or chemical used to transport a gene into a new host cell.

Attached at regular positions along this chain are nitrogen bases. Nitrogen bases are chemical compounds in which carbon, hydrogen, oxygen, and nitrogen atoms are arranged in rings. Four nitrogen bases occur in DNA: adenine (A), cytosine (C), guanine (G), and thymine (T).

The way in which nitrogen bases are arranged along a DNA molecule represents a kind of genetic code for the cell in which the molecule occurs. For example, the sequence of nitrogen bases T-T-C tells a cell that it should make the amino acid known as lysine. The sequence C-C-G, on the other hand, instructs the cell to make the amino acid glycine.

A very long chain (tens of thousands of atoms long) of nitrogen bases tells a cell, therefore, what amino acids to make and in what sequence to arrange those amino acids. A very long chain of amino acids arranged in a particular sequence, however, is what we know of as a protein. The specific sequence of nitrogen bases, then, tells a cell what kind of protein it should be making.

Furthermore, the instructions stored in a DNA molecule can easily be passed on from generation to generation. When a cell divides (reproduces), the DNA within it also divides. Each DNA molecule separates into two identical parts. Each of the two parts then makes a copy of itself. Where once only one DNA molecule existed, now two identical copies of the molecule exist. That process is repeated over and over again, every time a cell divides.

This discovery gave a chemical meaning to the term gene. According to our current understanding, a specific arrangement of nitrogen bases forms a code, or set of instructions, for a cell to make a specific protein. The protein might be the protein needed to make red hair, blue eyes, or wrinkled skin (to simplify the possibilities). The sequence of bases, then, holds the code for some genetic trait.

The Crick-Watson discovery opened up unlimited possibilities for biologists. If genes are chemical compounds, then they can be manipulated just as any other kind of chemical compound can be manipulated. Since DNA molecules are very large and complex, the actual task of manipulation may be difficult. However, the principles involved in working with DNA molecule genes is no different than the research principles with which all chemists are familiar.

For example, chemists know how to cut molecules apart and put them back together again. When these procedures are used with DNA molecules, the process is known as gene splicing. Gene splicing is a process that takes place naturally all the time in cells. In the process of division or repair, cells routinely have to take genes apart, rearrange their components, and put them back together again.

Scientists have discovered that cells contain certain kinds of enzymes that take DNA molecules apart and put them back together again. Endonucleases, for example, are enzymes that cut a DNA molecule at some given location. Exonucleases are enzymes that remove one nitrogen base unit at a time. Ligases are enzymes that join two DNA segments together.

It should be obvious that enzymes such as these can be used by scientists as submicroscopic scissors and glue with which one or more DNA molecules can be cut apart, rearranged, and the put back together again.

Genetic engineering requires three elements: the gene to be transferred, a host cell into which the gene is inserted, and a vector to bring about the transfer. Suppose, for example, that one wishes to insert the gene for making insulin into a bacterial cell. Insulin is a naturally occurring protein made by cells in the pancreas in humans and other mammals. It controls the breakdown of complex carbohydrates in the blood to glucose. People whose bodies have lost the ability to make insulin become diabetic.

The first step in the genetic engineering procedure is to obtain a copy of the insulin gene. This copy can be obtained from a natural source

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(from the DNA in a pancreas, for example), or it can be manufactured in a laboratory.

The second step in the process is to insert the insulin gene into the vector. The term vector means any organism that will carry the gene from one place to another. The most common vector used in genetic engineering is a circular form of DNA known as a plasmid. Endonucleases are used to cut the plasmid molecule open at almost any point chosen by the scientist. Once the plasmid has been cut open, it is mixed with the insulin gene and a ligase enzyme. The goal is to make sure that the insulin gene attaches itself to the plasmid before the plasmid is reclosed.

The hybrid plasmid now contains the gene whose product (insulin) is desired. It can be inserted into the host cell, where it begins to function just like all the other genes that make up the cell. In this case, however, in addition to normal bacterial functions, the host cell also is producing insulin, as directed by the inserted gene.

Notice that the process described here involves nothing more in concept than taking DNA molecules apart and recombining them in a different arrangement. For that reason, the process also is referred to as recombinant DNA (rDNA) research.

The possible applications of genetic engineering are virtually limitless. For example, rDNA methods now enable scientists to produce a number of products that were previously available only in limited quantities. Until the 1980s, for example, the only source of insulin available to diabetics was from animals slaughtered for meat and other purposes. The supply was never large enough to provide a sufficient amount of affordable insulin for everyone who needed insulin. In 1982, however, the U.S. Food and Drug Administration approved insulin produced by genetically altered organisms, the first such product to become available.

Since 1982, the number of additional products produced by rDNA techniques has greatly expanded. Among these products are human growth hormone (for children whose growth is insufficient because of genetic problems), alpha interferon (for the treatment of diseases), interleukin-2 (for the treatment of cancer), factor VIII (needed by hemophiliacs for blood clotting), erythropoietin (for the treatment of anemia), tumor necrosis factor (for the treatment of tumors), and tissue plasminogen activator (used to dissolve blood clots).

Genetic engineering also promises a revolution in agriculture. Recombinant DNA techniques enable scientists to produce plants that are resistant to herbicides and freezing temperatures, that will take longer to ripen, and that will manufacture a resistance to pests, among other characteristics.

Today, scientists have tested more than two dozen kinds of plants engineered to have special properties such as these. As with other aspects of genetic engineering, however, these advances have been controversial. The development of herbicide-resistant plants, for example, means that farmers are likely to use still larger quantities of herbicides. This trend is not a particularly desirable one, according to some critics. How sure can we be, others ask, about the risk to the environment posed by the introduction of "unnatural," engineered plants?

The science and art of animal breeding also are likely to be revolutionized by genetic engineering. For example, scientists have discovered that a gene in domestic cows is responsible for the production of milk. Genetic engineering makes it possible to extract that gene from cows who produce large volumes of milk or to manufacture that gene in the laboratory. The gene can then be inserted into other cows whose milk production may increase by dramatic amounts because of the presence of the new gene.

One of the most exciting potential applications of genetic engineering involves the treatment of human genetic disorders. Medical scientists know of about 3,000 disorders that arise because of errors in an individual's DNA. Conditions such as sickle-cell anemia, Tay-Sachs disease, Duchenne muscular dystrophy, Huntington's chorea, cystic fibrosis, and Lesch-Nyhan syndrome result from the loss, mistaken insertion, or change of a single nitrogen base in a DNA molecule. Genetic engineering enables scientists to provide individuals lacking a particular gene with correct copies of that gene. If and when the correct gene begins functioning, the genetic disorder may be cured. This procedure is known as human gene therapy (HGT).

The first approved trials of HGT with human patients began in the 1980s. One of the most promising sets of experiments involved a condition known as severe combined immune deficiency (SCID). Individuals with SCID have no immune systems. Exposure to microorganisms that would be harmless to the vast majority of people will result in diseases that can cause death. Untreated infants born with SCID who are not kept in a sterile bubble become ill within months and die before their first birthday.

In 1990, a research team at the National Institutes of Health (NIH) attempted HGT on a four-year-old SCID patient. The patient received about one billion cells containing a genetically engineered copy of the gene that his body lacked. Another instance of HGT was a procedure, approved in 1993 by NIH, to introduce normal genes into the airways of cystic fibrosis patients. By the end of the 1990s, according to the NIH, more than 390 gene therapy studies had been initiated. These studies involved more than 4,000 people and more than a dozen medical conditions.

In 2000, doctors in France claimed they had used HGT to treat three babies who suffered from SCID. Just ten months after being treated, the babies exhibited normal immune systems. This marked the first time that HGT had unequivocally succeeded.

Controversy remains. Human gene therapy is the source of great controversy among scientists and nonscientists alike. Few individuals maintain that the HGT should not be used. If we could wipe out sickle cell anemia, most agree, we should certainly make the effort. But HGT raises other concerns. If scientists can cure genetic disorders, they can also design individuals in accordance with the cultural and intellectual fashions of the day. Will humans know when to say "enough" to the changes that can be made with HGT?

Photo Researchers, Inc.

Despite recent successes, most results in HGT since the first experiment was conducted in 1990 have been largely disappointing. And in 1999, research into HGT was dealt a blow when an eighteen-year-old from Tucson, Arizona, died in an experiment at the University of Pennsylvania. The young man, who suffered from a metabolic disorder, had volunteered for an experiment to test gene therapy for babies with a fatal form of that disease. Citing the spirit of this young man, researchers remain optimistic, vowing to continue work into the possible lifesaving opportunities offered by HGT.

The commercial potential of genetically engineered products was not lost on entrepreneurs in the 1970s. A few individuals believed that the impact of rDNA on American technology would be comparable to that of computers in the 1950s. In many cases, the first genetic engineering firms were founded by scientists involved in fundamental research. The American biologist Herbert Boyer, for example, teamed up with the venture capitalist Robert Swanson in 1976 to form Genentech (Genetic Engineering Technology). Other early firms like Cetus, Biogen, and Genex were formed similarly through the collaboration of scientists and businesspeople.

The structure of genetic engineering (biotechnology) firms has, in fact, long been a source of controversy. Many observers have questioned the right of a scientist to make a personal profit by running companies that benefit from research that had been carried out at publicly funded universities. The early 1990s saw the creation of formalized working relations between universities, individual researchers, and the corporations founded by these individuals. Despite these arrangements, however, many ethical issues remain unresolved.

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Genetic Engineering - humans, body, used, process, plants ...

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

Human Nature on Collision Course with Genetic Engineering

Human genetic engineering could be the next major battleground for the global conservation movement, according to a series of reports in the latest issue of World Watch magazine, published by the Worldwatch Institute, a Washington, D.C.-based research organization. While previous struggles have involved protecting ecosystems and human societies from the unpredicted consequences of new technologies, this fight over high-risk applications of human genetic engineering is a struggle over who will decide what it means to be human.

Many countries have already banned reproductive cloning, and the U.N. is working on a global treaty to ban it, but even more powerful and much more dangerous are the related technologies to modify the genes we pass on to our children, says Ed Ayres, Editor of World Watch magazine. The contributors to this special issue call on the U.N. and national governments to ban the technology known as inheritable genetic modification.

Many uses of human genetic technology could be beneficial to society, but as political scientist Francis Fukuyama writes in the magazine, our understanding of the relationship between our genes and whatever improvements we might seek for our children (and their descendants) is dangerously deficient. Fukuyama warns that the victim of a failed experiment will not be an ecosystem, but a human child whose parents, seeking to give her greater intelligence, will saddle her with a greater propensity for cancer, or prolonged debility in old age, or some other completely unanticipated side effect that may emerge only after the experimenters have passed from the scene.

Human genetic engineering has ramifications that reach far beyond the life of a single child. Several contributors highlight the disastrous results of the last serious effort to engineer genetic perfection. In the early part of the 20th century, scientists and politicians in the United States relied on the alleged science of eugenics to justify the forced sterilization of tens of thousands of people who were judged to be feebleminded, mentally defective, or epileptics. Hitler passed his own sterilization law soon after taking office in 1933, heading down the path toward the Holocaust. The U.S. biotechnology industry-which dominates the global industry-has become an increasingly powerful economic and political force, with revenues growing fivefold between 1989 ($5 billion) and 2000 ($25 billion). Aided by the equally rapid revolution in computing, laboratories that once took two months to sequence 150 nucleotides can now process over 30 million in a day, and at a small fraction of the earlier cost. The number of patents pending for human DNA sequences has gone from 4,000 in 1991, to 500,000 in 1998, to several million today.

We are publishing this special issue because we dont want to lose the opportunity to decide openly and democratically how this rapidly developing technology is used, says Ayres. This isnt a fight about saving whales, or the last rain forests, or even the health of people living today. The question is whether we can save ourselves from ourselves, to know and respect what we do not know, and to put the breaks on potentially dangerous forms of human genetic engineering.

Excerpts from the authors of the Beyond Cloning issue of World Watch

About World Watch magazine: This bimonthly magazine is published by the Worldwatch Institute, an independent research organization, based in Washington, DC. Launched in 1988, the magazine has won the Alternative Press Award for investigative journalism, the Project Censored Award, and a number of Utne Reader awards. Recent editions have featured articles on the imminent disappearance of more than half of the worlds languages, airport sprawl, and the rapid growth of organic farming. Please visit: http://www.worldwatch.org/mag/.

The Worldwatch Institute is an independent research organization that works for an environmentally sustainable and socially just society, in which the needs of all people are met without threatening the health of the natural environment or the well-being of future generations. By providing compelling, accessible, and fact-based analysis of critical global issues, Worldwatch informs people around the world about the complex interactions between people, nature, and economies. Worldwatch focuses on the underlying causes of and practical solutions to the worlds problems, in order to inspire people to demand new policies, investment patterns, and lifestyle choices. For more information, visit: http://www.worldwatch.org.

Disclaimer: Please note that the statement by eight leaders of environmental NGOs, which appears on page 25 of the magazine, represents the views of the individuals quoted, not necessarily of the organizations they lead.

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Human Nature on Collision Course with Genetic Engineering ...

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 ...

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, also called genetic modification, is the direct manipulation of an organism's genome using biotechnology. It is therefore a set of technologies used to change the genetic makeup of cells, including the transfer of genes within and across species boundaries to produce improved or novel organisms. New DNA may be inserted in the host genome by first isolating and copying the genetic material of interest using molecular cloning methods to generate a DNA sequence, or by synthesizing the DNA, and then inserting this construct into the host organism. Genes may be removed, or "knocked out", using a nuclease. Gene targeting is a different technique that uses homologous recombination to change an endogenous gene, and can be used to delete a gene, remove exons, add a gene, or introduce point mutations.

An organism that is generated through genetic engineering is considered to be a genetically modified organism (GMO). The first GMOs were bacteria generated in 1973 and GM mice in 1974. Insulin-producing bacteria were commercialized in 1982 and genetically modified food has been sold since 1994. Glofish, the first GMO designed as a pet, was first sold in the United States December in 2003.[1]

Genetic engineering techniques have been applied in numerous fields including research, agriculture, industrial biotechnology, and medicine. Enzymes used in laundry detergent and medicines such as insulin and human growth hormone are now manufactured in GM cells, experimental GM cell lines and GM animals such as mice or zebrafish are being used for research purposes, and genetically modified crops have been commercialized.

IUPAC definition

Process of inserting new genetic information into existing cells in order to modify a specific organism for the purpose of changing its characteristics.

Note: Adapted from ref.[2][3]

Genetic engineering alters the genetic make-up of an organism using techniques that remove heritable material or that introduce DNA prepared outside the organism either directly into the host or into a cell that is then fused or hybridized with the host.[4] This involves using recombinant nucleic acid (DNA or RNA) techniques to form new combinations of heritable genetic material followed by the incorporation of that material either indirectly through a vector system or directly through micro-injection, macro-injection and micro-encapsulation techniques.

Genetic engineering does not normally include traditional animal and plant breeding, in vitro fertilisation, induction of polyploidy, mutagenesis and cell fusion techniques that do not use recombinant nucleic acids or a genetically modified organism in the process.[4] However the European Commission has also defined genetic engineering broadly as including selective breeding and other means of artificial selection.[5]Cloning and stem cell research, although not considered genetic engineering,[6] are closely related and genetic engineering can be used within them.[7]Synthetic biology is an emerging discipline that takes genetic engineering a step further by introducing artificially synthesized material from raw materials into an organism.[8]

If genetic material from another species is added to the host, the resulting organism is called transgenic. If genetic material from the same species or a species that can naturally breed with the host is used the resulting organism is called cisgenic.[9] Genetic engineering can also be used to remove genetic material from the target organism, creating a gene knockout organism.[10] In Europe genetic modification is synonymous with genetic engineering while within the United States of America it can also refer to conventional breeding methods.[11][12] The Canadian regulatory system is based on whether a product has novel features regardless of method of origin. In other words, a product is regulated as genetically modified if it carries some trait not previously found in the species whether it was generated using traditional breeding methods (e.g., selective breeding, cell fusion, mutation breeding) or genetic engineering.[13][14][15] Within the scientific community, the term genetic engineering is not commonly used; more specific terms such as transgenic are preferred.

Plants, animals or micro organisms that have changed through genetic engineering are termed genetically modified organisms or GMOs.[16] Bacteria were the first organisms to be genetically modified. Plasmid DNA containing new genes can be inserted into the bacterial cell and the bacteria will then express those genes. These genes can code for medicines or enzymes that process food and other substrates.[17][18] Plants have been modified for insect protection, herbicide resistance, virus resistance, enhanced nutrition, tolerance to environmental pressures and the production of edible vaccines.[19] Most commercialised GMO's are insect resistant and/or herbicide tolerant crop plants.[20] Genetically modified animals have been used for research, model animals and the production of agricultural or pharmaceutical products. They include animals with genes knocked out, increased susceptibility to disease, hormones for extra growth and the ability to express proteins in their milk.[21]

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Genetic engineering - Wikipedia, the free encyclopedia

QUESTION: What are the benefits of human genetic engineering?

ANSWER:

The benefits of human genetic engineering can be found in the headlines nearly every day. With the successful cloning of mammals and the completion of the Human Genome Project, scientists all over the world are aggressively researching the many different facets of human genetic engineering. These continuing breakthroughs have allowed science to more deeply understand DNA and its role in medicine, pharmacology, reproductive technology, and countless other fields.

The most promising benefit of human genetic engineering is gene therapy. Gene therapy is the medical treatment of a disease by repairing or replacing defective genes or introducing therapeutic genes to fight the disease. Over the past ten years, certain autoimmune diseases and heart disease have been treated with gene therapy. Many diseases, such as Huntington's disease, ALS (Lou Gehrig's disease), and cystic fibrosis are caused by a defective gene. The hope is that soon, through genetic engineering, a cure can be found for these diseases by either inserting a corrected gene, modifying the defective gene, or even performing genetic surgery. Eventually the hope is to completely eliminate certain genetic diseases as well as treat non-genetic diseases with an appropriate gene therapy.

Currently, many pregnant women elect to have their fetuses screened for genetic defects. The results of these screenings can allow the parents and their physician to prepare for the arrival of a child who may have special needs before, during, and after delivery. One possible future benefit of human genetic engineering is that, with gene therapy, a fetus w/ a genetic defect could be treated and even cured before it is born. There is also current research into gene therapy for embryos before they are implanted into the mother through in-vitro fertilization.

Another benefit of genetic engineering is the creation pharmaceutical products that are superior to their predecessors. These new pharmaceuticals are created through cloning certain genes. Currently on the market are bio-engineered insulin (which was previously obtained from sheep or cows) and human growth hormone (which in the past was obtained from cadavers) as well as bio-engineered hormones and blood clotting factors. The hope in the future is to be able to create plants or fruits that contain a certain drug by manipulating their genes in the laboratory.

The field of human genetic engineering is growing and changing at a tremendous pace. With these changes come several benefits and risks. These benefits and risks must be weighed in light of their moral, spiritual, legal, and ethical perspectives. The potential power of human genetic engineering comes with great responsibility.

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Benefits of Human Genetic Engineering - Popular Issues

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Human Genetics