www.nature.com/articles/s43587-023-00462-6
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Aging, often considered a result of random cellular damage, can be accurately estimated using DNA methylation profiles, the foundation of pan-tissue epigenetic clocks
demonstrate the development of universal pan-mammalian clocks, using 11,754 methylation arrays from our Mammalian Methylation Consortium
encompass 59 tissue types across 185 mammalian species
predictive models estimate mammalian tissue age with high accuracy (r > 0.96)
Age deviations correlate with human mortality risk
mouse somatotropic axis mutations and caloric restriction
identified specific cytosines with methylation levels that change with age across numerous species
sites, highly enriched in polycomb repressive complex 2-binding locations, are near genes implicated in mammalian development, cancer, obesity and longevity
aging is evolutionarily conserved and intertwined with developmental processes across all mammals
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