Adaptive responses of histone modifications to resistance exercise in human skeletal muscle

PLoS One. 2020 Apr 9;15(4):e0231321. doi: 10.1371/journal.pone.0231321. eCollection 2020.

Abstract

Exercise training causes epigenetic changes in skeletal muscle, although it is unclear how resistance exercise (RE) affects histone modifications. The present study was carried out to investigate the effects of acute RE and RE training on gene expression profiles and histone modifications in human skeletal muscle. Healthy male adults were assigned to acute RE (n = 9, age = 20.5±4.3yr, BMI = 28.0±6.8kg/m2) or RE training (n = 21, age = 23.7±2.5yr, BMI = 24.2±2.7kg/m2) groups. Biopsy samples were obtained from the vastus lateralis muscle before and three hours after a single bout of acute RE, or 3-days after 10 weeks of RE training. RNA sequencing analysis revealed that 153 genes with GO terms including muscle development, stress response, metabolism, cell death, and transcription factor were significantly up-regulated (+291% vs. pre-acute RE) upon acute RE. Expressions of these genes were also greater (+9.6% vs. pre-RE training, p<0.05) in RE trained subjects. Significant up-regulation of acetylated histone 3 (H3) (+235%) and H3 mono-methylated at lysine 4 (+290%) and tri-methylated at lysine 27 (+849%), whereas down-regulation of H3.3 variant (-39%) distributions relative to total H3 were observed at transcriptionally activated loci after acute RE compared to pre-acute RE levels. Interestingly, the distribution of acetylated H3 was found to be up-regulated as compared to the level of total H3 after RE training (+40%, p<0.05). These results indicate that a single bout of RE drastically alters both gene expressions and histone modifications in human skeletal muscle. It is also suggested that enhanced histone acetylation is closely related to up-regulation of gene expressions after RE training.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Adult
  • Down-Regulation
  • Exercise
  • Histones / metabolism*
  • Humans
  • Male
  • Methylation
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • RNA / chemistry
  • RNA / metabolism
  • Resistance Training*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Up-Regulation
  • Young Adult

Substances

  • Histones
  • Transcription Factors
  • RNA

Grants and funding

The present study was supported by Japan Society for the Promotion of Science KAKENHI Grant-in-Aid 16H03263 and 18H04987 to F. Kawano.