DNA去甲基化
5-甲基胞嘧啶
DNA甲基化
基底切除修复术
5-羟甲基胞嘧啶
去甲基化
化学
DNA修复
DNA复制
生物
胞嘧啶
DNA
DNA糖基化酶
甲基化
生物化学
基因
基因表达
作者
Rahul M. Kohli,Yi Zhang
出处
期刊:Nature
[Nature Portfolio]
日期:2013-10-23
卷期号:502 (7472): 472-479
被引量:1344
摘要
DNA methylation has a profound impact on genome stability, transcription and development. Although enzymes that catalyse DNA methylation have been well characterized, those that are involved in methyl group removal have remained elusive, until recently. The transformative discovery that ten-eleven translocation (TET) family enzymes can oxidize 5-methylcytosine has greatly advanced our understanding of DNA demethylation. 5-Hydroxymethylcytosine is a key nexus in demethylation that can either be passively depleted through DNA replication or actively reverted to cytosine through iterative oxidation and thymine DNA glycosylase (TDG)-mediated base excision repair. Methylation, oxidation and repair now offer a model for a complete cycle of dynamic cytosine modification, with mounting evidence for its significance in the biological processes known to involve active demethylation.
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