The interplay between DNA and histone methylation: molecular mechanisms and disease implications

被引:149
作者
Li, Yinglu [1 ,2 ]
Chen, Xiao [1 ,2 ]
Lu, Chao [1 ]
机构
[1] Columbia Univ, Irving Med Ctr, Dept Genet & Dev, New York, NY 10032 USA
[2] Columbia Univ, Irving Med Ctr, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
cancer; chromatin; developmental disorder; DNA methylation; histone methylation; DE-NOVO METHYLATION; LYSINE METHYLTRANSFERASE G9A; MAJOR SATELLITE REPEATS; REPRESSIVE COMPLEX 2; PWWP DOMAIN; DNMT3A MUTATIONS; STRUCTURAL BASIS; WEAVER SYNDROME; TUDOR DOMAIN; GENE EZH2;
D O I
10.15252/embr.202051803
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
Methylation of cytosine in CpG dinucleotides and histone lysine and arginine residues is a chromatin modification that critically contributes to the regulation of genome integrity, replication, and accessibility. A strong correlation exists between the genome-wide distribution of DNA and histone methylation, suggesting an intimate relationship between these epigenetic marks. Indeed, accumulating literature reveals complex mechanisms underlying the molecular crosstalk between DNA and histone methylation. These in vitro and in vivo discoveries are further supported by the finding that genes encoding DNA- and histone-modifying enzymes are often mutated in overlapping human diseases. Here, we summarize recent advances in understanding how DNA and histone methylation cooperate to maintain the cellular epigenomic landscape. We will also discuss the potential implication of these insights for understanding the etiology of, and developing biomarkers and therapies for, human congenital disorders and cancers that are driven by chromatin abnormalities.
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页数:21
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