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沙发

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发表于 2014-2-5 12:03:19
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Part II:Speed
【Time 2】
Article 2
Hungry Polar Bears Turn to Seabird Eggs
Polar bears are known for dining on whatever they want, from human garbage to reindeer to berries. But in the lower latitudes of the Canadian Arctic, they primarily prey on ringed seals (Pusa hispida), hunting them from sea ice platforms. Over the past 3 decades, however, the sea ice in this region has progressively broken up earlier than in the past due to climate change. The bears now face 2 months of ice-free habitat. Without seals to eat, the bears have increasingly turned to terrestrial prey, including the eggs of northern common eiders and thick-billed murres, scientists have discovered. Over three summers, from 2010 to 2012, researchers surveyed the birds’ nesting colonies on 230 islands and along more than 1000 kilometers of coastline in Hudson Strait and Northern Hudson Bay Narrows, looking for signs of predators. On 16 of the islands, they spotted 22 polar bears, and evidence of bears, such as feces containing eggshell, on an additional 63 islands, the researchers report online today in the Proceedings of the Royal Society B. They also watched bears eating eggs on numerous occasions (pictured). Overall, they found bears at 34% of the eider colonies, and estimated that the birds lost more eggs to them than to gulls and foxes, their usual nest predators. Murres, which nest on steep and narrow cliff ledges, are not as affected by the bears. The researchers do not yet know how the eiders will fare if the bears continue to feast on their eggs, although they think some colonies may go extinct if the intense predation continues. But their study—and others showing that polar bears are also dining on snow goose eggs and caribou—does support claims that polar bears in areas where the ice breaks up early don’t have enough time to hunt seals and acquire the fat reserves they need to make it through the ice-free season. The vanishing sea ice, the researchers conclude, is causing a cascade of unexpected ecological effects—not just on polar bears but also on seabirds.
Source:
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http://news.sciencemag.org/climate/2014/02/scienceshot-hungry-polar-bears-turn-seabird-eggs?rss=1
【Time 3】
Article 3
What Did Corn's Ancestor Really Look Like?
How did an ugly grass become one of the world’s most important crops? That’s a question researchers have been asking themselves ever since genetic analysis revealed that the ancestor of corn (right) was a spindly Mexican plant called teosinte (left). The answer is that ancient teosinte grew differently from its modern counterpart, according to a study published in Quaternary International. Researchers made the discovery by growing today’s teosinte in 20.1°C to 22.5°C greenhouses with 40% to 50% less carbon dioxide in the air—conditions more like those 14,000 years ago, when the plant was first domesticated. The plants grew shorter and had the female ears right on the main stem, the way they are in modern corn, instead of on side branches. And most of their seeds matured at once, while modern teosinte seeds mature over several weeks; the scientists kept having to go back to harvest them again and again. If teosinte used to be easier to harvest, domestication starts to make more sense. No sign of a cob, though; that must have come later.
字数[176]
Source:
http://news.sciencemag.org/plants-animals/2014/02/scienceshot-what-did-corns-ancestor-really-look
【Time 4】
Article 4
Monkeys born with edited genes
DNA-snipping technique inspired by bacteria shows therapeutic promise
The birth of two monkeys in China provides hope that a new type of gene therapy may one day help correct genetic defects in people.
The two cynomolgus monkeys, also known as crab-eating macaques, are the first primates to have their genes precisely edited using a gene-snipping tool borrowed from bacteria, a team of Chinese scientists reports January 30 in Cell. The work is part of an effort to genetically engineer monkeys to produce mutations like those seen in human diseases, especially ones involving the brain.
Other researchers have inserted foreign genes into primates (SN: 6/20/09, p. 13), but until now, no one has succeeded in altering the animals’ own genes, says Guoping Feng, a neurobiologist at the McGovern Institute for Brain Research at MIT who was not involved in the work.
To alter the monkeys’ genes, Jiahao Sha of Nanjing Medical University and his colleagues wielded molecular scissors first discovered in bacteria. The scissors are a DNA-cutting enzyme called Cas9. In bacteria, Cas9 is part of a primitive “immune system” — known as CRISPRs — that defends against viruses by chopping up ones that the bacteria have encountered before and recognize as threats.
The technique has been used to edit the genes of human cells growing in laboratory dishes and in rats, mice and other laboratory organisms, but never before in a living primate.
Sha, along with Xingxu Huang of Nanjing University and Weizhi Ji of the Yunnan Key Laboratory of Primate Biomedical Research and Kunming Biomed International, injected mRNA used to produce Cas9 into single-celled monkey embryos. At the same time, the researchers inserted other small RNA molecules that would guide the enzyme to three genes the scientists wanted to disrupt. Once the enzyme reached the genes, it would snip the DNA, leaving the cell to attempt a repair. In some cases, the cell would be unable to repair the break correctly, leading to disruption of the gene’s activity.
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【Time 5】
Researchers hope to use the technique to disrupt genes linked to human diseases so they can study how the disease develops and test treatments. For this study, the researchers chose three genes to disrupt: NrOb1, which is involved in keeping embryonic stem cells flexible and for determining sex; Ppar-gamma, which helps regulate metabolism; and Rag1, an immune system gene.
The researchers found that two of the three targeted genes had been simultaneously altered in eight of 15 injected embryos. Those eight embryos were transplanted into surrogate mothers. The researchers delivered the first two female babies, named Mingming and Ningning, from one of the surrogate moms on November 11, 2013. Both infants carry disrupted Ppar-gamma and Rag1 genes. Two of the other surrogates miscarried, and the researchers said in an e-mail that they are awaiting the birth of the remaining baby monkeys.
Only the targeted genes were disrupted, the researchers reported. That fact is encouraging, says Jennifer Doudna, a biochemist and Howard Hughes Medical Institute investigator at the University of California, Berkeley who is a pioneer of CRISPR techniques. It suggests that CRISPRs could be used to repair some human genes without inadvertently damaging others.
Feng agrees that the work suggests gene editing might one day fix some genetic defects in people by snipping out and replacing mutated DNA. “If you can put a mutation in, this suggests you can take a mutation out,” he said.
There are still problems to solve before the technology could ever be used in people, and even hurdles to using gene-edited monkeys as stand-ins for humans, he said. The technique was not as efficient as the researchers had hoped; they failed to disrupt one of the three targeted genes.
Another pitfall: Even though the researchers injected embryos at the single cell stage, the enzyme didn’t start snipping until the cells had divided, making the monkeys into mishmashes of cells with different mutations, and leaving some cells unaltered. Such mixed-up monkeys would confuse studies of any diseases they might be designed to mimic, so the researchers would need to wait years until the monkeys could breed and produce offspring with just one type of mutation in all their cells.
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Source:
https://www.sciencenews.org/article/monkeys-born-edited-genes
【Time 6】
Article 5
Drug Company Teaming With Yale to Share Trial Data
Johnson & Johnson announced an unusual partnership today with Yale University, in which it will share raw data from many of its clinical trials. The Yale University Open Data Access Project (aptly nicknamed YODA) will “review requests from investigators and physicians seeking access to anonymized clinical trials data from Janssen, the pharmaceutical companies of Johnson & Johnson,” the company wrote in a press release. YODA’s team will then decide which researchers can access the information for their own studies.
The announcement prompted a small explosion of news stories. Forbes wrote that “initially, this will only include products from the drug division, but it will expand to include devices and consumer products.” Janssen’s pharmaceutical products stretch the gamut, including pills for acid reflux, schizophrenia, pain, and birth control, among others. The data to be shared with YODA go well beyond study design and results, and include de-identified information on every volunteer. YODA is led by Harlan Krumholz, a cardiologist who has long pressed for more data access in clinical research. (In 2010, Forbes named him “The Most Powerful Doctor You Never Heard Of.”)
Johnson & Johnson, of course, will get to decide what it sends over to New Haven, although it’s pledging broad disclosure. That’s somewhat in contrast with a controversy brewing in Europe, where drug regulators are hoping to release the same kind of raw data submitted to it by pharmaceutical companies. That effort has been met with pushback and lawsuits. But it is part of a broader shift in both the United States and Europe, where researchers and some regulators are increasingly frustrated by the secrecy surrounding many drug trials, and want to get the information out in the open.
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Source:
http://news.sciencemag.org/health/2014/01/drug-company-teaming-yale-share-trial-data
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