Understanding the interplay between CpG island-associated gene promoters and H3K4 methylation

被引:91
作者
Hughes, Amy L. [1 ]
Kelley, Jessica R. [1 ]
Klose, Robert J. [1 ]
机构
[1] Univ Oxford, Dept Biochem, South Pk Rd, Oxford OX1 3QU, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2020年 / 1863卷 / 08期
基金
英国惠康基金; 欧洲研究理事会;
关键词
Chromatin; Transcription; DNA methylation; CpG islands; H3K4me3; TRANSCRIPTION START SITES; NOVO DNA METHYLATION; HISTONE-H3; LYSINE-4; METHYLATION; DOMAIN-CONTAINING PROTEINS; EMBRYONIC STEM-CELLS; PLANT HOMEODOMAIN; CXXC DOMAIN; PHD FINGER; SET DOMAIN; DYNAMIC ACETYLATION;
D O I
10.1016/j.bbagrm.2020.194567
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
The precise regulation of gene transcription is required to establish and maintain cell type-specific gene expression programs during multicellular development. In addition to transcription factors, chromatin, and its chemical modification, play a central role in regulating gene expression. In vertebrates, DNA is pervasively methylated at CG dinucleotides, a modification that is repressive to transcription. However, approximately 70% of vertebrate gene promoters are associated with DNA elements called CpG islands (CGIs) that are refractory to DNA methylation. CGIs integrate the activity of a range of chromatin-regulating factors that can post-translationally modify histones and modulate gene expression. This is exemplified by the trimethylation of histone H3 at lysine 4 (H3K4me3), which is enriched at CGI-associated gene promoters and correlates with transcriptional activity. Through studying H3K4me3 at CGIs it has become clear that CGIs shape the distribution of H3K4me3 and, in turn, H3K4me3 influences the chromatin landscape at CGIs. Here we will discuss our understanding of the emerging relationship between CGIs, H3K4me3, and gene expression.
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页数:15
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