Mat1 inhibits peroxisome proliferator-activated receptor gamma-mediated adipocyte differentiation

Mol Cell Biol. 2009 Jan;29(2):315-23. doi: 10.1128/MCB.00347-08. Epub 2008 Nov 3.

Abstract

Mammalian Cdk7, cyclin H, and Mat1 form the kinase submodule of transcription factor IIH (TFIIH) and have been considered ubiquitously expressed elements of the transcriptional machinery. Here we found that Mat1 and Cdk7 levels are undetectable in adipose tissues in vivo and downregulated during adipogenesis, where activation of peroxisome proliferator-activated receptor gamma (PPARgamma) acts as a critical differentiation switch. Using both Mat1(-/-) mouse embryonic fibroblasts and Cdk7 knockdown approaches, we show that the Cdk7 complex is an inhibitor of adipogenesis and is required for inactivation of PPARgamma through the phosphorylation of PPARgamma-S112. The results demonstrate that the Cdk7 submodule of TFIIH acts as a physiological roadblock to adipogenesis by inhibiting PPARgamma activity. The observation that components of TFIIH are absent from transcriptionally active adipose tissue prompts a reevaluation of the ubiquitous nature of basal transcription factors in mammalian tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / metabolism*
  • Adipogenesis* / genetics
  • Adipose Tissue, White / cytology
  • Adipose Tissue, White / metabolism
  • Amino Acid Transport Systems, Neutral / genetics
  • Amino Acid Transport Systems, Neutral / metabolism*
  • Animals
  • Cell Cycle Proteins
  • Cell Division
  • Cyclin-Dependent Kinase-Activating Kinase
  • Cyclin-Dependent Kinases / genetics
  • Cyclin-Dependent Kinases / metabolism*
  • Fibroblasts / metabolism
  • Mice
  • Mice, Knockout
  • PPAR gamma / metabolism*
  • Phosphorylation / physiology
  • Serine
  • Transcription Factor TFIIH / genetics
  • Transcription Factor TFIIH / metabolism*
  • Transcription Factors

Substances

  • Amino Acid Transport Systems, Neutral
  • Cell Cycle Proteins
  • Mnat1 protein, mouse
  • PPAR gamma
  • Transcription Factors
  • Transcription Factor TFIIH
  • Serine
  • Cyclin-Dependent Kinases
  • Cyclin-Dependent Kinase-Activating Kinase
  • Cdk7 protein, mouse