Dual control of mitochondrial biogenesis by sirtuin 1 and sirtuin 3

Mitochondrion. 2013 Nov;13(6):755-61. doi: 10.1016/j.mito.2013.04.002. Epub 2013 Apr 11.

Abstract

In this review, we discuss the dual control of mitochondrial biogenesis and energy metabolism by silent information regulator-1 and -3 (SIRT1 and SIRT3). SIRT1 activates the peroxisome proliferator activated receptor γ co-activator 1α (PGC-1α)-mediated transcription of nuclear and mitochondrial genes encoding for proteins promoting mitochondria proliferation, oxidative phosphorylation and energy production, whereas SIRT3 directly acts as an activator of proteins important for oxidative phosphorylation, tricarboxylic acid (TCA) cycle and fatty-acid oxidation and indirectly of PGC-1α and AMP-activated protein kinase (AMPK). The complex network involves different cellular compartments, transcriptional activation, post-translational modification and a plethora of secondary effectors. Overall, the mode of interaction between both sirtuin family members may be considered as a prominent case of molecular job-sharing.

Keywords: AMPK; FoxO3; Mitochondrial biogenesis; PGC-1α; Sirtuin; mtTFA.

Publication types

  • Review

MeSH terms

  • Acetylation
  • Adenylate Kinase / metabolism
  • Citric Acid Cycle
  • Humans
  • Mitochondria / metabolism*
  • Oxidative Phosphorylation
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Sirtuin 1 / metabolism*
  • Sirtuin 3 / metabolism*
  • Transcription Factors / antagonists & inhibitors
  • Transcription Factors / metabolism

Substances

  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Transcription Factors
  • Adenylate Kinase
  • SIRT1 protein, human
  • SIRT3 protein, human
  • Sirtuin 1
  • Sirtuin 3