Mitochondrial fusion is increased by the nuclear coactivator PGC-1beta

PLoS One. 2008;3(10):e3613. doi: 10.1371/journal.pone.0003613. Epub 2008 Oct 31.

Abstract

Background: There is no evidence to date on whether transcriptional regulators are able to shift the balance between mitochondrial fusion and fission events through selective control of gene expression.

Methodology/principal findings: Here, we demonstrate that reduced mitochondrial size observed in knock-out mice for the transcriptional regulator PGC-1beta is associated with a selective reduction in Mitofusin 2 (Mfn2) expression, a mitochondrial fusion protein. This decrease in Mfn2 is specific since expression of the remaining components of mitochondrial fusion and fission machinery were not affected. Furthermore, PGC-1beta increases mitochondrial fusion and elongates mitochondrial tubules. This PGC-1beta-induced elongation specifically requires Mfn2 as this process is absent in Mfn2-ablated cells. Finally, we show that PGC-1beta increases Mfn2 promoter activity and transcription by coactivating the nuclear receptor Estrogen Related Receptor alpha (ERRalpha).

Conclusions/significance: Taken together, our data reveal a novel mechanism by which mammalian cells control mitochondrial fusion. In addition, we describe a novel role of PGC-1beta in mitochondrial physiology, namely the control of mitochondrial fusion mainly through Mfn2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Fusion
  • Cells, Cultured
  • ERRalpha Estrogen-Related Receptor
  • GTP Phosphohydrolases / genetics
  • Gene Expression Regulation
  • HeLa Cells
  • Humans
  • Liver / metabolism
  • Mice
  • Mice, Knockout
  • Mitochondria / physiology*
  • Mitochondrial Size / genetics*
  • Muscle, Skeletal / metabolism
  • Myocardium / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Receptors, Estrogen / metabolism
  • Receptors, Estrogen / physiology
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription Factors
  • Transcription, Genetic

Substances

  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • Receptors, Estrogen
  • Trans-Activators
  • Transcription Factors
  • GTP Phosphohydrolases
  • Mfn2 protein, mouse