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Category Archives: Transhuman News

Germany Is Threatening Biohackers With Prison – Gizmodo

Posted: February 10, 2017 at 2:47 am

Over the last few years, advances in science have made the kind of experiments once only accessible to PhDs with fancy labs far more attainable. College undergrads are constructing gene drives. Anyone can buy a kit on the internet to concoct their own bioluminescent beer.

The German government, it seems, is none too pleased with this development. Two weeks ago its consumer protection office issued a statement making clear just how upset it is: Any science enthusiast doing genetic engineering outside of a licensed facility, it wrote, might face a fine of 50,000 or up to three years in prison.

The statement sent a wave of shock through the DIY bio community.

This is the first time Ive ever heard of a government calling out the DIY community specifically, said Todd Kuiken, a senior research scholar with the Genetic Engineering and Society Center at North Carolina State University.

The law behind the German DIY bio crackdown isnt new. The government was simply reminding so-called biohackers of a long-existing law that forbids genetic engineering experiments outside of laboratories supervised and licensed by the state.

But there is concern over how the pledge to enforce those rules may stymy the growth of the DIY science movement, and whether Germanys statement may inspire other European nations to take a similarly firm stance.

I am worried that the mentality could spread to other countries, said Josiah Zayner, who runs The Odin, a US company that sells DIY CRISPR kits.

Europe is generally much stricter in its regulation of genetic engineering and genetically modified products than the United States. In some countries, it is unclear whether DIY genetic engineering is legal at all.

A spokesperson for Germanys consumer protection office, the BVL, told Gizmodo that officials gathered in November to discuss concerns over the appearance of cheap DIY genetic engineering kits for sale on the internet, and decided it should issue a warning. Companies like The Odin and Amino Labs sell kits that make experimenting with DNA not much more difficult that whipping up a batch of brownies with a box of mix. Amino Labs compact, table-top bacteria lab is even sort of reminiscent of an Easybake oven, with its bright colors and playful name, the DNA Playground.

The statement has to be seen in light of the newly formed DIY biology scene and due to the appearance of low-priced DIY biology kits in online shops, the BVL told Gizmodo, via email.

At the moment, the BVL said it has not used the law to bring any criminal chargers against biohackers, though it may do so in the future.

Its difficult, but not impossible, for an individual in Germany to receive explicit government permission to do genetic engineering experiments outside of a lab. In Ireland, a PhD dropout named Cathal Garvey won such approval from the Irish government back in 2012.

Im pretty sure that laws will prohibit me from continuing my research at a later state, said Bruno Lederer, a German biohacker who hopes that loopholes in the law will allow his work to continue for now. I think its a shame that Id have to do illegal things in order to do independent research.

The BVL conceded that the new rules will make it virtually impossible for a lone scientist to meet the legal requirements to do genetic engineering. To begin with, any lab needs a project manager qualified by academic credentials such as a masters degree in science. Labs also require a commissioner for biological safety who is similarly qualified.

This makes genetic engineering experiments rather unattractive for individuals, the BVLs spokesman said.

Community biology labs, which often receive oversight and advisement from traditional scientists, shouldnt have an issue getting licensed. But not every DIY scientist lives near or has the resources to join a community lab. If the DIY bio movement is about making science accessible to those outside the Ivory Tower of academia, the German governments statement represents a serious roadblock.

If you are not living in a big city, access to a community biolab or an informal learning environment like a maker space is difficult, said Orkan Telhan, whose company, Biorealize, is in the process of developing its own DIY bio kits. There is no doubt that the field has to be regulated to mitigate adverse outcomes, but we need alternative ways to engage new audiences with biology.

In the US, biohackers operate in more of a regulatory gray areaoften regulations do not apply to them simply because no one ever conceived that self-taught scientists would one day pursue sophisticated biology experiments in their garages. But as the DIY community here has grown and sought to not just experiment at home, but sell its creations to the public, it, too, has increasingly faced regulatory run ins. In the US, DIY scientists are subject to the same rules as any other scientists. As in Germany, those regulations can be difficult to comply for an individual to comply with.

I dont think its entirely uncalled for to evaluate some of these spaces like community labs to make sure that they are operating in a safe manner, said Kuiken. I think that they are already operating safely, but currently there is no system in the US to determine that.

Germanys statement does offer one silver lining: it offers the rare clear guidance for what rules biohackers must comply with in order to go about their work legally.

Germany stating their position is a step forward in clarification, said Julie Legault of Amino Labs. Hopefully other countries will clarify their own rules as well.

The only question now is whether those rules will prevent biohackers from continuing with their work at all.

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New method of genetic engineering indispensable tool in … – Phys.org – Phys.Org

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February 9, 2017 by Kathryne Metcalf Restriction enzymes are essential tools for recombinant DNA technology that have revolutionized modern biological research, however have limited sequence specificity and availability. The Pyrococcus furiosus Argonaute (PfAgo) based platform for generating artificial restriction enzymes (AREs) is capable of recognizing and cleaving DNA sequences at virtually any arbitrary site and generating defined sticky ends of varying length. Credit: Behnam Enghiad and Huimin Zhao, University of Illinois at UrbanaChampaign

Research by Professor of Chemical and Biomolecular Engineering Huimin Zhao and graduate student Behnam Enghiad at the University of Illinois is pioneering a new method of genetic engineering for basic and applied biological research and medicine. Their work, reported in ACS Synthetic Biology on February 6, has the potential to open new doors in genomic research by improving the precision and adherence of sliced DNA.

"Using our technology, we can create highly active artificial restriction enzymes with virtually any sequence specificity and defined sticky ends of varying length," said Zhao, who leads a synthetic biology research group at the Carl R. Woese Institute for Genomic Biology at Illinois. "This is a rare example in biotechnology where a desired biological function or reagent can be readily and precisely designed in a rational manner."

Restriction enzymes are an important tool in genomic research: by cutting DNA at a specific site, they create a space wherein foreign DNA can be introduced for gene-editing purposes. This process is not only achieved by naturally-occurring restriction enzymes; other artificial restriction enzymes, or AREs, have risen to prominence in recent years. CRISPR-Cas9, a bacterial immune system used for "cut-and-paste" gene editing, and TALENs, modified restriction enzymes, are two popular examples of such techniques.

Though useful in genetic engineering, no AREs generate defined "sticky ends"an uneven break in the DNA ladder-structure that leaves complementary overhangs, improving adhesion when introducing new DNA. "If you can cleave two different DNA samples with the same restriction enzyme, the sticky ends that are generated are complementary," explained Enghiad. "They will hybridize with each other, and if you use a ligase, you can stick them together."

However, restriction enzymes themselves have a critical drawback: the recognition sequence which prompts them to cut is very shortusually only four to eight base pairs. Because the enzymes will cut anywhere that sequence appears, researchers rely on finding a restriction enzyme whose cut site appears only once in the genome of their organism or plasmidan often difficult proposition when the DNA at hand might be thousands of base pairs long.

This problem has been partially solved simply by the sheer number of restriction enzymes discovered: more than 3600 have been characterized, and over 250 are commercially available. "Just in our freezer, for our other research, we have probably over 100 different restriction enzymes," said Enghiad. "We look through them all whenever we want to assemble something ... the chance of finding the unique restriction site is so low.

"Our new technology unifies all of those restriction enzymes into a single system consisting of one protein and two DNA guides. Not only have you replaced them, but you can now target sites that no available restriction enzymes can."

Enghiad and Zhao's new technique creates AREs through the use of an Argonaute protein (PfAgo) taken from Pyrococcus furiosus, an archeal species. Led by a DNA guide, PfAgo is able to recognize much longer sequences when finding its cut site, increasing specificity and removing much of the obstacles posed by restriction enzymes. Further, PfAgo can create longer sticky ends than even restriction enzymes, a substantial benefit as compared to other AREs.

"When we started, I was inspired by a paper about a related proteinTtAgo. It could use a DNA guide to cleave DNA, but only up to 70 degrees," explained Enghiad. "DNA strands start to separate over 75 degrees, which could allow a protein to create sticky ends. If there were a protein that was active at higher temperatures, I reasoned, that protein could be used as an artificial restriction enzyme.

"So I started looking for that, and what I found was PfAgo."

In addition to replacing restriction enzymes in genetic engineering processes, Enghiad and Zhao believe their technology will have broad applications in the biological research. By creating arbitrary sticky ends, PfAgo could make assembly of large DNA molecules easier, and enables cloning of large DNA molecules such as biochemical pathways and large genes.

The application of these techniques is broad-reaching: ranging from discovery of new small molecule drugs to engineering of microbial cell factories for synthesis of fuels and chemicals to molecular diagnostics of genetic diseases and pathogens, which are the areas Zhao and Enghiad are currently exploring.

"Due to its unprecedented simplicity and programmability (a single protein plus DNA guides for targeting), as well as accessibility ... we expect PfAgo-based AREs will become a powerful and indispensable tool in all restriction enzyme or nuclease-enabled biotechnological applications and fundamental biological research," said Zhao. "It is to molecular biology as the CRISPR technology is to cell biology."

Explore further: Prevention of RNA virus replication

More information: Behnam Enghiad et al, Programmable DNA-Guided Artificial Restriction Enzymes, ACS Synthetic Biology (2017). DOI: 10.1021/acssynbio.6b00324

Researchers at Okayama University have successfully cleaved influenza viral RNA to prevent its replication using novel artificial RNA restriction enzymes in laboratory cell cultures. While further improvements are needed, ...

Better tools for manipulating DNA in the laboratory may soon be possible with newly discovered deoxyribozymes (catalytic DNA) capable of cleaving single-stranded DNA, researchers at the University of Illinois say.

Scientists have shed new light on the way superbugs such as MRSA are able to become resistant to treatment with antibiotics.

Genetic engineering of plants, animals and microorganisms such as bacteria typically involves the use of restriction enzymes to 'cut and paste' DNA fragments into certain genetic sequence locations. This process allows scientists ...

Researchers at the University of Minnesota have discovered a molecular security system in human cells that deactivates and degrades foreign DNA. This discovery could open the door to major improvements in genetic engineering ...

By consuming fewer calories, ageing can be slowed down and the development of age-related diseases such as cancer and type 2 diabetes can be delayed. The earlier calorie intake is reduced, the greater the effect. Researchers ...

Research by Professor of Chemical and Biomolecular Engineering Huimin Zhao and graduate student Behnam Enghiad at the University of Illinois is pioneering a new method of genetic engineering for basic and applied biological ...

The bacterial world is rife with unusual talents, among them a knack for producing electricity. In the wild, "electrogenic" bacteria generate current as part of their metabolism, and now researchers at the University of California, ...

Chemists have developed a powerful new method of selectively linking chemicals to proteins, a major advance in the manipulation of biomolecules that could transform the way drugs are developed, proteins are probed, and molecules ...

Understanding how oil and gas molecules, water and rocks interact at the nanoscale will help make extraction of hydrocarbons through hydraulic fracturing more efficient, according to Rice University researchers.

Researchers from the University of Maryland College Park (UMD) and Baltimore (UMB) campuses have developed a blood test that could help doctors more quickly diagnose schizophrenia and other disorders. Their study, "Redox ...

Scientists at The Australian National University (ANU) have controlled wave-generated currents to make previously unimaginable liquid materials for new technological innovations, including techniques to manipulate micro-organisms.

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Genetics of both virus and patient work together to influence the … – Science Daily

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Genetics of both virus and patient work together to influence the ...
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Viral and human genetics together account for about one third of the differences in disease progression rates seen among people infected with the human ...
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Medical College of Wisconsin names director of Human and Molecular Genetics Center – Wauwatosa Now

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The Medical College of Wisconsin (MCW) appointed Raul A. Urrutia as director of the Human and Molecular Genetics Center and professor of the Department of Surgery, effective July 1.

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Wauwatosa 4:17 p.m. CT Feb. 9, 2017

Business brief(Photo: Matt Colby/Now Media Group)

The Medical College of Wisconsin (MCW) appointed Raul A. Urrutia as director of the Human and Molecular Genetics Center and professor of the Department of Surgery, effective July 1.

Urrutia currently serves as professor in the departments of biochemistry and molecular biology, biophysics and medicine at the Mayo Clinic College of Medicine in Rochester, Minnesotaand director of epigenomics education and academic relationships in the epigenomics program, Mayo Clinic Center for Individualized Medicine.

Urrutia will relocatefrom Rochester, Minnesota, with his wifeGwen Lomberk, who will serve as associate professor, chief of the division of research, and director of basic research in the MCW Department of Surgery.

Read or Share this story: http://www.wauwatosanow.com/story/news/local/2017/02/09/medical-college-wisconsin-names-director-human-and-molecular-genetics-center/97714872/

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The tragic story of Soviet genetics shows the folly of political meddling in science – Cosmos

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A few years ago, one of us (Ian) was lucky enough to be invited to visit the N.I. Vavilov Institute of Plant Industry in St Petersburg, Russia. Every plant breeder or geneticist knows of Nikolai Vavilov and his ceaseless energy in collecting important food crop varieties from all over the globe, and his application of genetics to plant improvement.

Vavilov championed the idea that there were Centres of Origin (or Diversity) for all plant species, and that the greatest variation was to be found in the place where the species evolved: wheat from the Middle East; coffee from Ethiopia; maize from Central America, and so on.

Hence the Centres of Origin (commonly known as the Vavilov Centres) are where you should start looking to find genotypes the set of genes responsible for a particular trait with disease resistance, stress tolerance or any other trait you are looking for. This notion applies to any species, which is why you can find more human genetic variation in some African countries than in the rest of the world combined.

By the late 1920s, as director of the Lenin All-Union Academy of Agricultural Sciences, Vavilov soon amassed the largest seed collection on the planet. He worked hard, he enjoyed himself, and drove other eager young scientists to work just as hard to make more food for the people of the Soviet Union.

However, things did not go well for Vavilov politically. How did this visionary geneticist, who aimed to find the means for food security, end up starving to death in a Soviet gulag in 1943?

Enter the villain, Trofim Lysenko, ironically a protg of Vavilovs. The notorious Vavilov-Lysenko antagonism became one of the saddest textbook examples of a futile effort to resolve scientific debate using a political approach.

Lysenkos name leapt from the pages of history and into the news when Australias Chief Scientist, Alan Finkel, mentioned him during a speech at a meeting of chief scientists in Canberra this week.

Finkel was harking back to Lysenko in response to news that US President Donald Trump had acted in January to censor scientific data regarding climate change from the Environmental Protection Agency. Lysenkos story reminds us of the dangers of political interference in science, said Finkel:

Lysenko believed that successive generations of crops could be improved by exposing them to the right environment, and so too could successive generations of Soviet citizens be improved by exposing them to the right ideology.

So while Western scientists embraced evolution and genetics, Russian scientists who thought the same were sent to the gulag. Western crops flourished. Russian crops failed.

The emerging ideology of Lysenkoism was effectively a jumble of pseudoscience, based predominantly on his rejection of Mendelian genetics and everything else that underpinned Vavilovs science. He was a product of his time and political situation in the young USSR.

In reality, Lysenko was what we might today call a crackpot. Among other things, he denied the existence of DNA and genes, he claimed that plants selected their mates, and argued that they could acquire characteristics during their lifetime and pass them on. He also espoused the theory that some plants choose to sacrifice themselves for the good of the remaining plants another notion that runs against the grain of evolutionary understanding.

Pravda formerly the official newspaper of the Soviet Communist Party celebrated him for finding a way to fertilise crops without applying anything to the field.

None of this could be backed up by solid evidence. His experiments were not repeatable, nor could his theories claim overwhelming consensus among other scientists. But Lysenko had the ear of the one man who counted most in the USSR: Joseph Stalin.

The Lysenko vs Vavilov/Mendel/Darwin argument came to a head in 1936 at the Conference of the Lenin Academy when Lysenko presented his -ism.

In the face of scientific opinion, and the overwhelming majority of his peers, Pravda declared Lysenko the winner of the argument. By 1939, after quite a few scientists had been imprisoned, shot or disappeared, including the director of the Lenin Institute, there was a vacancy to be filled. And the most powerful man in the country filled it with Trofim Lysenko. Lysenko was now Vavilovs boss.

Within a year, Vavilov was captured on one of his collection missions and interrogated for 11 months. He was accused of being a spy, having travelled to England and the United States, and been a regular correspondent with many geneticists outside the Soviet Union.

It did not help his cause that he came from a family of business people, whereas Lysenko was of peasant stock and a Soviet ideologue. Vavilov was sent to a gulag where, tragically, he died in 1943.

Meanwhile, his collection in Leningrad was in the middle of a 900-day siege. It only survived thanks to the sacrifice of his team who formed a militia to prevent the starving population (and rats) from eating the collection of more than 250,000 types of seeds, fruits and roots even growing the potatoes in their stock near the front to ensure the tubers did not die before losing their viability.

In 1948, the Lenin Academy announced that Lysenkoism should be taught as the only correct theory, and that continued until the mid-1960s.

Thankfully, in the post-Stalin era, Lysenko was slowly sidelined along with his theory. Today it is Vavilov who is considered a Soviet hero.

In 1958, the Academy of Science began awarding a medal in his honour. The leading Russian plant science institute is named in his honour, as is the Saratov State Vavilov Agrarian University. In addition, an asteroid, a crater on the Moon and two glaciers bear his name.

Since 1993, Bioversity International has awarded Vavilov Frankel (after Australian scientist Otto Frankel) fellowships to young scientists from developing countries to perform innovative research on plant genetic resources.

Meanwhile, research here in Australia, led by ARC Discovery Early Career Fellow Lee Hickey, we are continuing to find new genetic diversity for disease resistance in the Vavilov wheat collection.

In the post-Soviet era, students of genetics and agriculture in Russia are taught of the terrible outcomes of the applications of Lysenkoism to Soviet life and agricultural productivity.

Lysenkoism is a sad and terrible footnote in agricultural research, more important as a sadly misused -ism in the hands of powerful people who opt for ideology over fact. Its also a timely reminder of the dangers of political meddling in science.

Ian Godwin, Professor in Plant Molecular Genetics, The University of Queensland and Yuri Trusov, Plant molecular biologist, The University of Queensland

This article was originally published on The Conversation and republished here with permission. Read the original article.

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DNA saves dog from death penalty – CNN

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Jeb's owners, Penny and Kenneth Job of St. Clair, Michigan, couldn't believe that their sweet Jeb, the same gentle dog who helps Ken get up when he falls down, who lives peacefully with three other dogs, seven cats and a coopful of chickens, could ever harm another living being.

So the family used a forensic technique often used for human defendants to save their dog from death row last fall.

Jeb Stuart Job stands hip-high, with a muscular frame, big dark eyes and a long black snout. He's had a rough two years on this Earth.

In January 2016, when he wasn't quite a year old, he was found chained inside a shed in Detroit. His owner had died, and the rest of the family didn't want him.

Kandie Morrison, a volunteer with a dog rescue agency, got the call.

Once Morrison met Jeb, she thought he'd make the perfect service dog for her father; that's Kenneth Job.

Job, 79, an Air Force veteran who owned a drywall business, has a neurodegenerative disease called Charcot-Marie-Tooth. He fell in love with the Belgian Malinois puppy. Dr. Karen Pidick, their veterinarian and neighbor in their rural Michigan town, trained Jeb to help Job stay steady on his shaky legs.

The family was a happy one until eight months later.

According to court testimony, on the morning of August 24, the Jobs' neighbor, Christopher Sawa, looked out his kitchen window and saw Jeb standing over the lifeless body of his own dog, Vlad.

Vlad weighed 14 pounds. Jeb weighed about 90 pounds.

Sawa ran out into his yard. He tried to give Vlad mouth-to-mouth resuscitation, but it was too late. The tiny Pomeranian was dead.

Sawa called animal control and blamed Jeb. Animal control took the big dog into custody.

On September 19, all parties gathered at district court in St. Clair County.

If Judge Michael Hulewicz deemed Jeb a "dangerous animal," the dog would be put to death.

Sawa, the Jobs' neighbor for more than 30 years, testified about finding Jeb standing over his dead Pomeranian.

"It was horrifying. It was terrifying," he said, according to transcripts. CNN contacted the Sawas, who declined to comment.

He said it wasn't the first time Jeb had scared him.

"I was afraid of the dog. The dog always barked," he said.

Now, his beloved Vlad was gone.

"We've never had any children," he testified. "The dog was like a child to us."

Job testified that Jeb had indeed gotten away from him that morning: He and the Jobs' other three dogs had run off in the opposite direction of the Sawa home, toward a house with a pond where they liked to swim.

The Jobs' attorney, Edward Marshall, pointed to a lack of physical evidence linking Jeb to Vlad's death and questioned whether another large animal had killed Vlad. After all, Pidick, the neighborhood vet, had testified that an unfriendly stray dog had been spotted in the neighborhood, and foxes were known to live in the surrounding woods.

In the end, the judge said Jeb met the legal definition of a dangerous animal, and he made what he said was a tough decision.

"I have no choice except to follow out the state law that the animal would be destroyed," Hulewicz said. "I don't like to do this. I don't like it at all."

That's when the Job family asked to have testing done to see whether Jeb's DNA matched the DNA in Vlad's wound. They said they hadn't asked for it sooner because they thought Vlad had been cremated and there would be no way to get his DNA.

But at the trial, it came out that Vlad's body was in a freezer.

The Jobs arranged to have swabs taken from Vlad's wound and the inside of Jeb's cheek. The samples were sent to the Maples Center for Forensic Medicine at the University of Florida College of Medicine. The process cost $416, according to the Jobs.

On October 24, exactly two months after Jeb was taken into custody, AnnMarie Clark, a forensic DNA analyst at the center, sent in her findings: The DNA in the wound didn't match Jeb's DNA.

"Jeb is not the dog that killed (Vlad)," Clark wrote.

"We were relieved. We were absolutely relieved," said Penny Job, Ken's wife.

The DNA showed that another dog had killed Jeb, Clark told CNN -- but exactly who that dog is may forever be a mystery.

Jeb was allowed to go home the following week, after his owners signed an agreement promising that they would make sure Jeb wouldn't leave the yard unleashed and that they would maintain a secure fence to keep their animals in the yard.

The Jobs say Jeb came home a very different dog.

They say that during his nine weeks in animal control, he went from 90 to 75 pounds, and he became scared and skittish.

"The dog was thin and sick," Penny Job said. "And he lost all his social skills. He was afraid to go outside."

Jeb's weight wasn't taken when he entered and left animal control, said Steve Campau, a spokesman for the St. Clair County sheriff's office, which oversees animal control.

"We fed him a meal day," Campau said. "Maybe he was overfed at home."

Campau also said some behavior changes are to be expected after an animal is released from spending nine weeks of spending 23 hours a day in a kennel that's 6 feet long by 3 feet wide.

"Veterinarians say after a dog is in a kennel environment for an extended period of time, there's certainly going to be an adjustment period when the dog gets out," Campau said.

Even now, more than three months after his return home, Jeb is still scared of strange men, his owners say.

Still bitter that their innocent dog was nearly put to death, Jeb's owners wonder why they had to come up with the idea of DNA analysis. Why didn't the court do it before condemning Jeb to death? After all, that kind of testing is often done with human defendants.

Humans accused of a crime have rights under criminal due process.

"In a criminal prosecution, where you're putting a person in jail, we have the highest level of protection," Favre said.

It's a different story with dogs.

"Dogs have no rights. They're property," Favre said.

He wonders whether courts should reconsider and make DNA analysis a regular part of the process when a dog's life hangs in the balance.

"It's an easy thing to do. We just haven't thought of it in this context," he said.

He applauds the Jobs for saving their pet.

"Now people will realize they can do this, that it's a tool," he said. "They used a very creative defense."

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Push for Contentious DNA Method Outlasts the Case Calling for It – New York Times

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Push for Contentious DNA Method Outlasts the Case Calling for It
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When law enforcement officials began a push to use an ethically complicated forensic technique involving DNA in New York, they based their appeal on a high-profile case that had gone unsolved for months: the murder of Karina Vetrano, a 30-year-old ...
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DNA links Riverside man to 2001 gang rape in Yucaipa, sheriff’s … – Redlands Daily Facts

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YUCAIPA >> Detectives finally got a break in a 16-year-old rape case thanks to DNA.

In July 2001, a woman reported she had been walking near California Street and Avenue E when four men pulled alongside her and forced her into their vehicle, according to a sheriffs news release. They drove her to a remote location and gang raped her, the news release said.

During the investigation DNA was collected as evidence and entered into the Combined DNA Index System database, but there wasnt a match at the time of the incident.

The case went cold. Then someone was arrested on an unrelated crime last November, bringing the case back to the surface, according to sheriffs officials.

Jose Angel Bueno, 47, of Riverside, was arrested for an unrelated crime. His DNA was taken by Riverside authorities and sent to the Department of Justice to be added into the national database.

Buenos sample came back as a match to the DNA collected from the unsolved 2001 rape case, officials said.

Detectives found Bueno in custody at West Valley Detention Center Wednesday on an unrelated case. They booked him for suspicion of rape and kidnapping with the intent to commit rape. Hes being held in lieu of $1 million bail.

Detectives believe there may be more victims that havent come forward.

Anyone with information is asked to call sheriffs detectives at 909-918-2305.

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An ‘ignition key’ revs up DNA shuffling to make antibodies … – Science Daily

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An 'ignition key' revs up DNA shuffling to make antibodies ...
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Rearranging the genome is a risky endeavor, and human cells reserve it for special occasions, like making egg and sperm cells.

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Circular DNA Helps Cancer Roll with the Therapeutic Punches – Genetic Engineering & Biotechnology News

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In the evolution of cancer, the most vicious circle may be that perpetrated by circular DNA, which is also known as extrachromosomal DNA (ecDNA). According to a new study, ecDNA is found in nearly half of all types of tumors, and it encodes multiple copies of driver oncogenes, or cancer-driving genes. Worse, driver oncogenes appear to be more harmful in ecDNA than in chromosomal DNA. Driver oncogenes in ecDNA contribute to tumor heterogeneity and drug resistance.

These new findings appeared February 8 in the journal Nature, in an article entitled, Extrachromosomal Oncogene Amplification Drives Tumour Evolution and Genetic Heterogeneity. The article indicates that ecDNA, once thought to be rare in tumor cells, is actually very common and seems to play a fundamental role in tumor evolution. The articles main pointthat ecDNA contributes to accelerated evolution in cancercould lead to new ways to prevent and treat many malignancies

The Nature paper is based on a study led by an interdisciplinary team led jointly by Paul Mischel, M.D., a member of the Ludwig Institute for Cancer Research, and Vineet Bafna, Ph.D., a professor at the University of California San Diego School of Medicine. The scientists analyzed cells from 17 different types of cancer to explore ecDNA. They also analyzed the structure and function of chromosomes of 2572 dividing cells during metaphase, and they developed a software package called ECdetect to conduct unbiased, integrated ecDNA detection and analysis.

Here we show that ecDNA was found in nearly half of human cancers; its frequency varied by tumour type, but it was almost never found in normal cells, wrote the authors of the Nature paper. Driver oncogenes were amplified most commonly in ecDNA, thereby increasing transcript level.

Essentially, the researchers showed that ecDNA plays a far bigger role in the growth, diversity, and drug resistance of cancer cells than the same genes housed on chromosomes in such tumors.

Weve discovered something fundamental about how cancers diversify and evolve, said Mischel. This is an essential rethinking about what goes wrong with genes in cancer.

The Nature paper describes how the scientists performed whole-genome sequencing, structural modeling, and cytogenetics to detect, quantify, and analyze ecDNA. They found that ecDNA was present in about 40% of tumor cell lines, but was extremely rare in normal cells. And when the scientists looked specifically at patient-derived models of brain tumors, nearly 90% of these carried ecDNA. The researchers also found that oncogenes are more likely to occur on ecDNA than on chromosomes.

Mathematical modelling predicted that ecDNA amplification would increase oncogene copy number and intratumoural heterogeneity more effectively than chromosomal amplification, the authors added. We validated these predictions by quantitative analyses of cancer samples and verified their models predictions through experiments conducted on tumor samples from patients.

These studies revealed that tumors are more heterogeneous when oncogenes are amplified on ecDNA instead of on chromosomes, enabling them to more rapidly achieve and maintain high levels of cancer promoting genes.

Unlike chromosomes, ecDNA is parceled out randomly to daughter cells when a tumor cell divides. So, any given cell in a tumor might have no ecDNA in its nucleus, or it might be crammed with ecDNA. And the greater the variation in oncogene copy number, the greater the heterogeneity of cells in a tumor. It is this cellular diversity that makes tumors far more resistant to environmental challenges, most notably drug therapy.

The new work was inspired by a previous study led by Mischel and reported in Science in 2014. In that study, Mischel and colleagues revealed that ecDNA plays a central role in the drug resistance of certain brain tumors.

This finding came as a surprise because, for decades, cancer biologists had focused more on which genes promote cancer rather than where those genes are located. Genomic technologies too evolved along lines that favored this type of analysis. Although a few cancer biologists in the 1960s had described the presence of ecDNA in some tumor cells, they lacked the tools to quantify ecDNA, so the phenomenon had long been considered rare and inconsequential to the development of cancer.

It occurred to us after we made the observations published in 2014 that maybe ecDNA is a lot more common and consequential than anyone thought, explained Mischel. Understanding how tumor cells evolve and how they increase the copy number and variability of their drivers is likely to yield some pretty important clues about the fundamental biology of cancer and how we might be able to target it.

Mischel his team are now working to unearth the molecular mechanisms involved in the genesis and maintenance of ecDNA and exploring how ecDNA levels change in response to changes in the tumors internal environment.

Excerpt from:
Circular DNA Helps Cancer Roll with the Therapeutic Punches - Genetic Engineering & Biotechnology News

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