后代
DNA甲基化
生物
甲基化
遗传学
生殖系
表观遗传学
自闭症
精子
基因
心理学
基因表达
怀孕
精神科
作者
Maria H. Milekic,Yurong Xin,Anne O’Donnell‐Luria,K K Kumar,Maria Bradley-Moore,Dolores Malaspina,Helen Moore,Daniela Brunner,Yulin Ge,John R. Edwards,Swagatika Paul,Fatemeh Haghighi,Jay A. Gingrich
摘要
Advanced paternal age (APA) has been shown to be a significant risk factor in the offspring for neurodevelopmental psychiatric disorders, such as schizophrenia and autism spectrum disorders. During aging, de novo mutations accumulate in the male germline and are frequently transmitted to the offspring with deleterious effects. In addition, DNA methylation during spermatogenesis is an active process, which is susceptible to errors that can be propagated to subsequent generations. Here we test the hypothesis that the integrity of germline DNA methylation is compromised during the aging process. A genome-wide DNA methylation screen comparing sperm from young and old mice revealed a significant loss of methylation in the older mice in regions associated with transcriptional regulation. The offspring of older fathers had reduced exploratory and startle behaviors and exhibited similar brain DNA methylation abnormalities as observed in the paternal sperm. Offspring from old fathers also had transcriptional dysregulation of developmental genes implicated in autism and schizophrenia. Our findings demonstrate that DNA methylation abnormalities arising in the sperm of old fathers are a plausible mechanism to explain some of the risks that APA poses to resulting offspring.
科研通智能强力驱动
Strongly Powered by AbleSci AI