A Comprehensive Review of Structural Insights into DNA Methylation Maintenance.

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Amika Kikuchi, Kyohei Arita
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引用次数: 0

Abstract

DNA methylation is faithfully inherited during cell division, playing a crucial role in maintaining cellular identity. The process of DNA methylation maintenance relies on DNA methyltransferase DNMT1 and the ubiquitin E3 ligase UHRF1. UHRF1 facilitates the ubiquitination of both the replication factor PAF15 and histone H3, with each ubiquitin signal regulating replication-coupled and uncoupled DNA methylation maintenance, respectively. Over the past decades, advances in structural biology have significantly deepened our understanding of the molecular mechanisms governing DNA methylation maintenance. In particular, the emergence of cryo-electron microscopy (cryo-EM)-often referred to as the "Resolution Revolution"-has transformed many areas of biology, including epigenetics and chromatin biology. This review focuses on the structural mechanisms of DNA methylation maintenance, as revealed by the three-dimensional structures of key biomolecular complexes and discusses the potential development of inhibitors targeting DNA methylation maintenance factors based on structural insights.

DNA甲基化维持的结构研究综述。
DNA甲基化在细胞分裂过程中忠实地遗传,在维持细胞身份中起着至关重要的作用。DNA甲基化维持过程依赖于DNA甲基转移酶DNMT1和泛素E3连接酶UHRF1。UHRF1促进复制因子PAF15和组蛋白H3的泛素化,每个泛素信号分别调节复制偶联和非偶联DNA甲基化维持。在过去的几十年里,结构生物学的进步大大加深了我们对控制DNA甲基化维持的分子机制的理解。特别是,冷冻电子显微镜(cryo-EM)的出现-通常被称为“分辨率革命”-已经改变了生物学的许多领域,包括表观遗传学和染色质生物学。本文综述了DNA甲基化维持的结构机制,以及关键生物分子复合物的三维结构,并讨论了基于结构见解的DNA甲基化维持因子抑制剂的潜在开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genes & genetic systems
Genes & genetic systems 生物-生化与分子生物学
CiteScore
1.50
自引率
0.00%
发文量
22
审稿时长
>12 weeks
期刊介绍: Genes & Genetic Systems , formerly the Japanese Journal of Genetics , is published bimonthly by the Genetics Society of Japan.
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