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The control of gene expression and cell identity by H3K9 trimethylation
Author(s) -
Maria Ninova,
Katalin Fejes Tóth,
Alexei A. Aravin
Publication year - 2019
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.181180
Subject(s) - biology , heterochromatin , histone , heterochromatin protein 1 , chromatin , genetics , gene silencing , chromodomain , sumo protein , regulation of gene expression , histone h3 , microbiology and biotechnology , epigenetics , gene , rna , helicase , ubiquitin
Histone 3 lysine 9 trimethylation (H3K9me3) is a conserved histone modification that is best known for its role in constitutive heterochromatin formation and the repression of repetitive DNA elements. More recently, it has become evident that H3K9me3 is also deposited at certain loci in a tissue-specific manner and plays important roles in regulating cell identity. Notably, H3K9me3 can repress genes encoding silencing factors, pointing to a fundamental principle of repressive chromatin auto-regulation. Interestingly, recent studies have shown that H3K9me3 deposition requires protein SUMOylation in different contexts, suggesting that the SUMO pathway functions as an important module in gene silencing and heterochromatin formation. In this Review, we discuss the role of H3K9me3 in gene regulation in various systems and the molecular mechanisms that guide the silencing machinery to target loci.

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