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
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-06-18
卷期号:392 (6804): eaea4922-eaea4922
被引量:1
标识
DOI:10.1126/science.aea4922
摘要
Age and early life adversity (ELA) are key determinants of health, but whether they affect similar physiological mechanisms across tissues is unknown. We generated DNA methylation (DNAm) profiles across 14 tissues in 237 semi-free-ranging rhesus macaques with naturally occurring ELA. Age-associated DNAm was predominantly tissue dependent, yet tissue-specific epigenetic clocks showed that epigenetic aging was relatively consistent within individuals. ELA effects were adversity dependent, but each ELA exerted coordinated effects across tissues. Although ELA targeted many of the same loci as age, the directions of effects differed, which indicates that ELA does not uniformly increase epigenetic age. Instead, ELA leaves a coordinated, cross-tissue epigenetic signature that is distinct from-yet intertwined with-age-related differences, which advances our understanding of how early environments sculpt the molecular foundations of aging and disease.
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