染色质重塑
DNA甲基化
生物
体育锻炼的表观遗传学
MECP2
组蛋白
染色质
组蛋白甲基化
细胞生物学
遗传学
基因
基因表达
表型
作者
Keri Martinowich,Daisuke Hattori,Hao Wu,Shaun D. Fouse,Fei He,Yan Hu,Guoping Fan,Yi Sun
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2003-10-31
卷期号:302 (5646): 890-893
被引量:1313
标识
DOI:10.1126/science.1090842
摘要
In conjunction with histone modifications, DNA methylation plays critical roles in gene silencing through chromatin remodeling. Changes in DNA methylation perturb neuronal function, and mutations in a methyl-CpG–binding protein, MeCP2, are associated with Rett syndrome. We report that increased synthesis of brain-derived neurotrophic factor (BDNF) in neurons after depolarization correlates with a decrease in CpG methylation within the regulatory region of the Bdnf gene. Moreover, increased Bdnf transcription involves dissociation of the MeCP2–histone deacetylase–mSin3A repression complex from its promoter. Our findings suggest that DNA methylation–related chromatin remodeling is important for activity-dependent gene regulation that may be critical for neural plasticity.
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