表观遗传学
DNA甲基化
生物
生物年龄
后生
进化生物学
甲基化
遗传学
加速老化
衰老
细胞老化
计算生物学
健康衰老
生物信息学
作者
Subin Jang,Seongjun Kim,Dayeon Kang,Chae‐Yeon Hong,Eun‐Yeong Bok,Sung‐Lim Lee,Yong‐Ho Choe,Jaemin Kim
标识
DOI:10.1073/pnas.2528874123
摘要
Aging is accompanied by both increasing interindividual heterogeneity and systematic, age-associated alterations in DNA methylation (DNAm). Here, we investigated these complementary dimensions of epigenetic aging in dogs using global and locus-specific measures of epigenetic drift alongside clock-based estimates of biological aging. We observed pervasive, yet genomically structured epigenetic instability throughout the canine lifespan. The extent of age-associated epigenetic drift further varied by body size, suggesting biological stratification of methylation instability. Cross-national comparison of clock-derived epigenetic age acceleration (EAA) between South Korea and the United States revealed consistently higher EAA in Korean dogs, with sex-associated differences detected within the Korean cohort. We further identified CpGs with cohort-specific age-associated methylation patterns, indicating that population-level differences in epigenetic aging extend beyond clock-based estimates to locus-specific methylation dynamics. Together, these findings highlight population-level diversity in canine epigenetic aging and support dogs as a tractable model for investigating biological and environmental determinants of age-related epigenetic change.
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