Differential expression of HDAC and HAT genes in atrophying skeletal muscle

Muscle Nerve. 2015 Dec;52(6):1098-101. doi: 10.1002/mus.24912. Epub 2015 Oct 10.

Abstract

Introduction: Histone deacetylase (HDAC) proteins, which counter the activity of histone acetyltransferases (HATs), are necessary for normal muscle atrophy in response to several pathophysiological conditions. Despite this, it remains unknown whether a common or unique transcriptional profile of HDAC and HAT genes exist during the progression of muscle atrophy.

Methods: Muscles were harvested from cast immobilized, denervated, or nutrient deprived animals for quantitative reverse transcriptase-polymerase chain reaction analysis of HDAC and HAT gene expression.

Results: The mRNA levels of Hdac2, Hdac4, Hdac6, Sirt1, p300, Cbp, and Pcaf increased, and Hdac7 decreased in skeletal muscle in each experimental model of muscle atrophy. Hdac1 and Hdac3 were increased only in cast immobilized and denervated muscles.

Conclusions: While specific HDACs and HATs are increased in multiple models of muscle atrophy, increased expression of class I HDACs was unique to muscle disuse, reinforcing that specific HDAC inhibitors may be more effective than pan-HDAC inhibitors at countering muscle atrophy.

Keywords: denervation; histone acetyltransferase; histone deacetylase; muscle disuse; muscle wasting.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Disease Models, Animal
  • Gene Expression Regulation / physiology*
  • Histone Acetyltransferases / genetics
  • Histone Acetyltransferases / metabolism*
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Muscular Atrophy / etiology
  • Muscular Atrophy / metabolism*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Restraint, Physical / adverse effects

Substances

  • RNA, Messenger
  • Histone Acetyltransferases
  • Histone Deacetylases