Regulation of skeletal muscle development and homeostasis by gene imprinting, histone acetylation and microRNA

被引:46
|
作者
Moresi, Viviana [1 ]
Marroncelli, Nicoletta [1 ]
Coletti, Dario [1 ]
Adamo, Sergio [1 ]
机构
[1] Univ Roma La Sapienza, Dept Anat Histol Forens & Orthop Sci, Sect Histol & Med Embryol, I-00161 Rome, Italy
关键词
HDACs; HDACi; DNA methylase; MyomiRs; DUCHENNE MUSCULAR-DYSTROPHY; SATELLITE CELL ACTIVATION; NOVO DNA METHYLATION; NON-CPG METHYLATION; DEACETYLASE INHIBITORS; MOUSE MODEL; CATALYTIC-ACTIVITY; ADP-RIBOSYLATION; STEM; EXPRESSION;
D O I
10.1016/j.bbagrm.2015.01.002
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
Epigenetics is defined as heritable information other than the DNA sequence itself. The concept implies that the regulation of gene expression is a highly complex process in which epigenetics plays a major role that ranges from fine-tuning to permanent gene activation/deactivation. Skeletal muscle is the main tissue involved in locomotion and energy metabolism in the body, accounting for at least 40% of the body mass. Body mass and function vary according to age but also quickly adapt to both physiological and pathological cues. Besides transcriptional mechanisms that control muscle differentiation, postnatal growth and remodeling, there are numerous epigenetic mechanisms of regulation that modulate muscle gene expression. In this review, we describe and discuss only some of the mechanisms underlying epigenetic regulation, such as DNA methylation, histone modifications and microRNAs, which we believe are crucial to skeletal muscle development and disease. (C) 2015 The Authors. Published by Elsevier B.V.
引用
收藏
页码:309 / 316
页数:8
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