Age-related sperm DNA methylation changes are transmitted to offspring and associated with abnormal behavior and dysregulated gene expression

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
出处
期刊:Molecular Psychiatry [Springer Nature]
卷期号:20 (8): 995-1001 被引量:168
标识
DOI:10.1038/mp.2014.84
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.
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