Transcriptomic Signatures and Upstream Regulation in Human Skeletal Muscle Adapted to Disuse and Aerobic Exercise

Int J Mol Sci. 2021 Jan 26;22(3):1208. doi: 10.3390/ijms22031208.

Abstract

Inactivity is associated with the development of numerous disorders. Regular aerobic exercise is broadly used as a key intervention to prevent and treat these pathological conditions. In our meta-analysis we aimed to identify and compare (i) the transcriptomic signatures related to disuse, regular and acute aerobic exercise in human skeletal muscle and (ii) the biological effects and transcription factors associated with these transcriptomic changes. A standardized workflow with robust cut-off criteria was used to analyze 27 transcriptomic datasets for the vastus lateralis muscle of healthy humans subjected to disuse, regular and acute aerobic exercise. We evaluated the role of transcriptional regulation in the phenotypic changes described in the literature. The responses to chronic interventions (disuse and regular training) partially correspond to the phenotypic effects. Acute exercise induces changes that are mainly related to the regulation of gene expression, including a strong enrichment of several transcription factors (most of which are related to the ATF/CREB/AP-1 superfamily) and a massive increase in the expression levels of genes encoding transcription factors and co-activators. Overall, the adaptation strategies of skeletal muscle to decreased and increased levels of physical activity differ in direction and demonstrate qualitative differences that are closely associated with the activation of different sets of transcription factors.

Keywords: disuse; exercise; extracellular matrix; heterodimer; mitochondrion; skeletal muscle; transcription factors; transcriptome.

MeSH terms

  • Adaptation, Physiological*
  • Computational Biology / methods
  • Exercise*
  • Gene Expression Profiling*
  • Gene Expression Regulation*
  • Gene Regulatory Networks
  • Humans
  • Molecular Sequence Annotation
  • Muscle, Skeletal / metabolism*
  • Phenotype
  • Resistance Training
  • Transcriptome*