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[Histone H3K27me3 in the regulation of skeletal muscle development].

Authors :
Gan YM
Zhou J
Quan R
Hong LJ
Li ZC
Zheng EQ
Liu W
Wu ZF
Cai GY
Gu T
Source :
Yi chuan = Hereditas [Yi Chuan] 2019 Apr 20; Vol. 41 (4), pp. 285-292.
Publication Year :
2019

Abstract

Histone methylation is a modification which occurs in the N-terminal peptide chains of the histone nucleosome. The 4th, 9th, 27th, 36th and 79th lysines in N-terminal peptide chain of histone H3 are hot spots for this modification, including mono-, di-, and tri-methylation. H3K27me3 is the tri-methylation modification on histone H3 lysine 27, which mainly functions as a transcriptional repressor regulating skeletal muscle development. Studies have shown that H3K27me3 can finely regulate skeletal muscle proliferation, including the level and duration of skeletal muscle development by specifically binding to myogenic regulatory factors (e.g., MyoD, MyoG, etc.), cell cycling regulators, and epigenetic regulators including lncRNA and miRNA. In this review, we introduce the types and mechanisms of histone methylation and de-methylation of H3K27. We also summarize how H3K27me3 functions in the proliferation and differentiation of skeletal muscle cell. This review will contribute to the comprehension of the function of H3K27me3 in regulating skeletal muscle development and provide reference for further improving our understanding of mammalian muscle.

Details

Language :
Chinese
ISSN :
0253-9772
Volume :
41
Issue :
4
Database :
MEDLINE
Journal :
Yi chuan = Hereditas
Publication Type :
Academic Journal
Accession number :
30992250
Full Text :
https://doi.org/10.16288/j.yczz.18-272