表观基因组
德纳姆
表观遗传学
DNA甲基化
生物
后生
进化生物学
生物年龄
遗传学
基因
基因表达
作者
Baptiste Sadoughi,Rachel M. Petersen,Sam K. Patterson,Elizabeth Slikas,Christine Adjandba,Nicholas Ryan,Christina E. Costa,Laura Newman,Marina M. Watowich,Cameron R. Kelsey,Ashlee Greenier,Elisabeth A. Goldman,Josué E. Negrón-Del Valle,Daniel Phillips,Indya Thompson,Samuel E. Bauman Surratt,Olga González,Nicole Compo,Armando Burgos-Rodriguez,Alex R. DeCasien
标识
DOI:10.1101/2025.07.13.664445
摘要
Age and early life adversity (ELA) are both key determinants of health, but whether they target similar physiological mechanisms across the body is unknown due to limited multi-tissue datasets from well-characterized cohorts. We generated DNA methylation (DNAm) profiles across 14 tissues in 237 semi-free ranging rhesus macaques, with records of naturally occurring ELA. We show that age-associated DNAm variation is predominantly tissue-dependent, yet tissue-specific epigenetic clocks reveal that the pace of epigenetic aging is relatively consistent within individuals. ELA effects on loci are adversity-dependent, but a given ELA has a coordinated impact across tissues. Finally, ELA targeted many of the same loci as age, but the direction of these effects varied, indicating that ELA does not uniformly contribute to accelerated age in the epigenome. ELA thus imprints a coordinated, tissue-spanning epigenetic signature that is both distinct from and intertwined with age-related change, advancing our understanding of how early environments sculpt the molecular foundations of aging and disease.
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