Department of Biostatistics, Fielding School of Public Health, University of California, Los Angeles, Los Angeles, CA, USA.
Johnson & Johnson Innovative Medicine, Spring House, PA, USA.
Sci Adv. 2024 Jun 7;10(23):eadm7273. doi: 10.1126/sciadv.adm7273.
By analyzing 15,000 samples from 348 mammalian species, we derive DNA methylation (DNAm) predictors of maximum life span ( = 0.89), gestation time ( = 0.96), and age at sexual maturity ( = 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.
通过分析来自 348 种哺乳动物的 15000 个样本,我们得出了预测最大寿命(=0.89)、妊娠期(=0.96)和性成熟年龄(=0.85)的 DNA 甲基化(DNAm)预测因子。我们的最大寿命预测因子表明,在包括人类在内的 17 种哺乳动物中,女性可能具有先天的长寿优势。DNAm 最大寿命预测不受热量限制或部分重编程的影响。生长激素受体等躯体轴的遗传破坏仅在某些组织中对 DNAm 最大寿命产生影响。癌症死亡率与我们对生命史特征的表观遗传估计没有相关性。DNAm 最大寿命预测因子无法检测同一物种个体之间的寿命差异,例如狗的不同品种之间。最大寿命部分取决于一种内在的物种特性的表观遗传特征,与与个体死亡风险相关的特征不同。