DNA甲基化
表观遗传学
CpG站点
生物
DNA去甲基化
体育锻炼的表观遗传学
运动前神经元活动
甲基化
神经发生
神经科学
表观遗传学
DNA
基因
遗传学
基因表达
作者
Junjie U. Guo,K. Dengke,Huan Mo,Mad Price Ball,Mi Hyeon Jang,Michael A. Bonaguidi,Jacob A. Balazer,Hugh L. Eaves,Bo Xie,Eric Ford,Kun Zhang,Ming Guo,Yuan Gao,Hongjun Song
摘要
DNA methylation has been traditionally viewed as a highly stable epigenetic mark in postmitotic cells. However, postnatal brains appear to show stimulus-induced methylation changes, at least in a few identified CpG dinucleotides. How extensively the neuronal DNA methylome is regulated by neuronal activity is unknown. Using a next-generation sequencing-based method for genome-wide analysis at single-nucleotide resolution, we quantitatively compared the CpG methylation landscape of adult mouse dentate granule neurons in vivo before and after synchronous neuronal activation. About 1.4% of 219,991 CpGs measured showed rapid active demethylation or de novo methylation. Some modifications remained stable for at least 24 h. These activity-modified CpGs showed a broad genomic distribution with significant enrichment in low-CpG density regions, and were associated with brain-specific genes related to neuronal plasticity. Our study implicates modification of the neuronal DNA methylome as a previously underappreciated mechanism for activity-dependent epigenetic regulation in the adult nervous system.
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