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

Biochim Biophys Acta. 2015 Mar;1849(3):309-16. doi: 10.1016/j.bbagrm.2015.01.002. Epub 2015 Jan 15.

Abstract

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.

Keywords: DNA methylase; HDACi; HDACs; MyomiRs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acetylation
  • DNA Methylation
  • Epigenesis, Genetic*
  • Genomic Imprinting*
  • Histones
  • Homeostasis / genetics
  • Humans
  • MicroRNAs
  • Muscle Development / genetics*
  • Muscle, Skeletal / growth & development*
  • Muscle, Skeletal / metabolism
  • Protein Processing, Post-Translational / genetics

Substances

  • Histones
  • MicroRNAs