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脊椎动物中DNA修复与5-甲基胞嘧啶的擦除

DNA repair and erasure of 5-methylcytosine in vertebrates.

作者信息

Schomacher Lars, Niehrs Christof

机构信息

Institute of Molecular Biology (IMB), Mainz, Germany.

Division of Molecular Embryology, German Cancer Research Center-Zentrum für Molekulare Biologie der Universität Heidelberg (DKFZ-ZMBH) Alliance, Heidelberg, Germany.

出版信息

Bioessays. 2017 Mar;39(3). doi: 10.1002/bies.201600218. Epub 2017 Jan 18.

Abstract

DNA methylation plays important roles in development and disease. Yet, only recently has the dynamic nature of this epigenetic mark via oxidation and DNA repair-mediated demethylation been recognized. A major conceptual challenge to the model that DNA methylation is reversible is the risk of genomic instability, which may come with widespread DNA repair activity. Here, we focus on recent advances in mechanisms of TET-TDG mediated demethylation and cellular strategies that avoid genomic instability. We highlight the recently discovered involvement of NEIL DNA glycosylases, which cooperate with TDG in oxidative demethylation to accelerate substrate turnover and promote the organized handover of harmful repair intermediates to maintain genome stability.

摘要

DNA甲基化在发育和疾病中发挥着重要作用。然而,直到最近,这种表观遗传标记通过氧化和DNA修复介导的去甲基化的动态性质才被认识到。DNA甲基化是可逆的这一模型面临的一个主要概念性挑战是基因组不稳定的风险,这可能伴随着广泛的DNA修复活性。在这里,我们关注TET-TDG介导的去甲基化机制以及避免基因组不稳定的细胞策略的最新进展。我们强调了最近发现的NEIL DNA糖基化酶的参与,它与TDG在氧化去甲基化中协同作用,以加速底物周转,并促进有害修复中间体的有序交接,从而维持基因组稳定性。

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