Decreased transcriptional corepressor p107 is associated with exercise-induced mitochondrial biogenesis in human skeletal muscle

Physiol Rep. 2017 Mar;5(5):e13155. doi: 10.14814/phy2.13155.

Abstract

Increased mitochondrial content is a hallmark of exercise-induced skeletal muscle remodeling. For this process, considerable evidence underscores the involvement of transcriptional coactivators in mediating mitochondrial biogenesis. However, our knowledge regarding the role of transcriptional corepressors is lacking. In this study, we assessed the association of the transcriptional corepressor Rb family proteins, Rb and p107, with endurance exercise-induced mitochondrial adaptation in human skeletal muscle. We showed that p107, but not Rb, protein levels decrease by 3 weeks of high-intensity interval training. This is associated with significant inverse association between p107 and exercise-induced improved mitochondrial oxidative phosphorylation. Indeed, p107 showed significant reciprocal correlations with the protein contents of representative markers of mitochondrial electron transport chain complexes. These findings in human skeletal muscle suggest that attenuated transcriptional repression through p107 may be a novel mechanism by which exercise stimulates mitochondrial biogenesis following exercise.

Keywords: OXPHOS; Exercise; Rb family; human; mitochondrial biogenesis.

MeSH terms

  • Adult
  • Exercise / physiology*
  • Humans
  • Male
  • Muscle, Skeletal / metabolism*
  • Organelle Biogenesis*
  • Oxidative Phosphorylation
  • Physical Endurance / physiology
  • Retinoblastoma Protein / genetics
  • Retinoblastoma Protein / metabolism
  • Retinoblastoma-Like Protein p107 / genetics
  • Retinoblastoma-Like Protein p107 / metabolism*
  • Young Adult

Substances

  • RBL1 protein, human
  • Retinoblastoma Protein
  • Retinoblastoma-Like Protein p107