德纳姆
生物
长寿
寿命
表观遗传学
DNA甲基化
进化生物学
重编程
遗传学
动物
生理学
基因
基因表达
作者
Caesar Z. Li,Amin Haghani,Qi Yan,Ake T. Lu,Joshua Zhang,Zhe Fei,Jason Ernst,X. William Yang,Vadim N. Gladyshev,Todd R. Robeck,Andreas S. Chavez,Joseph A. Cook,Jonathan L. Dunnum,Ken Raj,Andrei Seluanov,Vera Gorbunova,Steve Horvath
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2024-06-07
卷期号:10 (23): eadm7273-eadm7273
被引量:26
标识
DOI:10.1126/sciadv.adm7273
摘要
By analyzing 15,000 samples from 348 mammalian species, we derive DNA methylation (DNAm) predictors of maximum life span ( R = 0.89), gestation time ( R = 0.96), and age at sexual maturity ( R = 0.85). Our maximum life-span predictor indicates a potential innate longevity advantage for females over males in 17 mammalian species including humans. The DNAm maximum life-span predictions are not affected by caloric restriction or partial reprogramming. Genetic disruptions in the somatotropic axis such as growth hormone receptors have an impact on DNAm maximum life span only in select tissues. Cancer mortality rates show no correlation with our epigenetic estimates of life-history traits. The DNAm maximum life-span predictor does not detect variation in life span between individuals of the same species, such as between the breeds of dogs. Maximum life span is determined in part by an epigenetic signature that is an intrinsic species property and is distinct from the signatures that relate to individual mortality risk.
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