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Longevity Tied to Genes That Preserve Tips of ChromosomesA team led by researchers at Albert Einstein College of Medicine of Yeshiva University has found a clear link between living to 100 and inheriting a hyperactive version of an enzyme that rebuilds telomeres—the tip ends of chromosomes. The findings appear in the Proceedings of the National Academy of Sciences. Telomeres play crucial roles in aging, cancer, and other biological processes. They are relatively short sections of specialized DNA that sit at the ends of all chromosomes. Each time a cell divides, its telomeres erode slightly and become progressively shorter with each cell division. Eventually, telomeres become so short that their host cells stop dividing and lapse into a condition called cell senescence. As a result, vital tissues and important organs begin to fail and the classical signs of aging ensue. In investigating the role of telomeres in aging, the Einstein researchers studied Ashkenazi Jews because they are a homogeneous population that was already well-studied genetically. Three groups were enrolled: 86 very old, but generally healthy, people (average age 97); 175 of their offspring; and 93 controls (offspring of parents who had lived a normal lifespan). “Telomeres are one piece of the puzzle that accounts for why some people can live so long,” says Gil Atzmon, PhD, an assistant professor of medicine and of genetics at Einstein, Genetic Core Leader for The LonGenity Project at Einstein’s Institute for Aging Research, and a lead author of the paper. The answer to both questions was “yes.” “As we suspected, humans of exceptional longevity are better able to maintain the length of their telomeres,” said Yousin Suh, PhD, an associate professor of medicine and of genetics at Einstein and senior author of the paper. “And we found that they owe their longevity, at least in part, to advantageous variants of genes involved in telomere maintenance.” More specifically, the researchers found that participants who have lived to a very old age have inherited mutant genes that make their telomerase-making system extra active and able to maintain telomere length more effectively. For the most part, these people were spared age-related diseases such as cardiovascular disease and diabetes, which cause most deaths among elderly people. — Source: Albert Einstein College of Medicine of Yeshiva University |






