Mechanisms of DNA Methylation Regulatory Function and Crosstalk with Histone Lysine Methylation

被引:4
|
作者
Tibben, Bailey M. [1 ]
Rothbart, Scott B. [1 ]
机构
[1] Van Andel Inst, Dept Epigenet, Grand Rapids, MI 49503 USA
基金
美国国家卫生研究院;
关键词
DNA methylation; histone methylation; gene regulation; cancer; neurodevelopmental disorders; METHYLTRANSFERASE GENE DNMT3A; MAJOR SATELLITE REPEATS; ACUTE MYELOID-LEUKEMIA; DE-NOVO METHYLATION; SOMATIC MUTATIONS; OVERGROWTH SYNDROME; H3K36; METHYLATION; PRC2; COMPLEX; PWWP DOMAIN; CPG ISLANDS;
D O I
10.1016/j.jmb.2023.168394
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation is a well-studied epigenetic modification that has key roles in regulating gene expression, maintaining genome integrity, and determining cell fate. Precisely how DNA methylation patterns are established and maintained in specific cell types at key developmental stages is still being elucidated. However, research over the last two decades has contributed to our understanding of DNA methylation regulation by other epigenetic processes. Specifically, lysine methylation on key residues of histone proteins has been shown to contribute to the allosteric regulation of DNA methyltransferase (DNMT) activities. In this review, we discuss the dynamic interplay between DNA methylation and histone lysine methylation as epigenetic regulators of genome function by synthesizing key recent studies in the field. With a focus on DNMT3 enzymes, we discuss mechanisms of DNA methylation and histone lysine methylation crosstalk in the regulation of gene expression and the maintenance of genome integrity. Further, we discuss how alterations to the balance of various sites of histone lysine methylation and DNA methylation contribute to human developmental disorders and cancers. Finally, we provide perspectives on the current direction of the field and highlight areas for continued research and development. (c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:31
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