Peroxisome proliferator-activated receptor-gamma coactivator-1alpha controls transcription of the Sirt3 gene, an essential component of the thermogenic brown adipocyte phenotype

J Biol Chem. 2011 May 13;286(19):16958-66. doi: 10.1074/jbc.M110.202390. Epub 2011 Mar 27.

Abstract

Sirt3 (silent mating type information regulation 2, homolog 3), a member of the sirtuin family of protein deacetylases with multiple actions on metabolism and gene expression is expressed in association with brown adipocyte differentiation. Using Sirt3-null brown adipocytes, we determined that Sirt3 is required for an appropriate responsiveness of cells to noradrenergic, cAMP-mediated activation of the expression of brown adipose tissue thermogenic genes. The transcriptional coactivator Pgc-1α (peroxisome proliferator-activated receptor-γ coactivator-1α) induced Sirt3 gene expression in white adipocytes and embryonic fibroblasts as part of its overall induction of a brown adipose tissue-specific pattern of gene expression. In cells lacking Sirt3, Pgc-1α failed to fully induce the expression of brown fat-specific thermogenic genes. Pgc-1α activates Sirt3 gene transcription through coactivation of the orphan nuclear receptor Err (estrogen-related receptor)-α, which bound the proximal Sirt3 gene promoter region. Errα knockdown assays indicated that Errα is required for full induction of Sirt3 gene expression in response to Pgc-1α. The present results indicate that Pgc-1α controls Sirt3 gene expression and this action is an essential component of the overall mechanisms by which Pgc-1α induces the full acquisition of a brown adipocyte differentiated phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Cell Nucleus / metabolism
  • Cloning, Molecular
  • Cyclic AMP / metabolism
  • ERRalpha Estrogen-Related Receptor
  • Fibroblasts / cytology
  • Gene Expression Regulation*
  • Mice
  • Mice, Inbred C57BL
  • Models, Biological
  • Phenotype
  • RNA, Messenger / metabolism
  • Receptors, Estrogen / metabolism
  • Sirtuin 3 / metabolism*
  • Transcription Factors / metabolism*

Substances

  • RNA, Messenger
  • Receptors, Estrogen
  • Sirt3 protein, mouse
  • Transcription Factors
  • peroxisome-proliferator-activated receptor-gamma coactivator-1
  • Cyclic AMP
  • Sirtuin 3