p38 mitogen-activated protein kinase is the central regulator of cyclic AMP-dependent transcription of the brown fat uncoupling protein 1 gene

Mol Cell Biol. 2004 Apr;24(7):3057-67. doi: 10.1128/MCB.24.7.3057-3067.2004.

Abstract

It is well established that catecholamine-stimulated thermogenesis in brown fat requires beta-adrenergic elevations in cyclic AMP (cAMP) to increase expression of the uncoupling protein 1 (UCP1) gene. However, little is known about the downstream components of the signaling cascade or the relevant transcription factor targets thereof. Here we demonstrate that cAMP- and protein kinase A-dependent activation of p38 mitogen-activated protein kinase (MAPK) in brown adipocytes is an indispensable step in the transcription of the UCP1 gene in mice. By phosphorylating activating transcription factor 2 (ATF-2) and peroxisome proliferator-activated receptor gamma (PPARgamma) coativator 1alpha (PGC-1alpha), members of two distinct nuclear factor families, p38 MAPK controls the expression of the UCP1 gene through their respective interactions with a cAMP response element and a PPAR response element that both reside within a critical enhancer motif of the UCP1 gene. Activation of ATF-2 by p38 MAPK additionally serves as the cAMP sensor that increases expression of the PGC-1alpha gene itself in brown adipose tissue. In conclusion, our findings illustrate that by orchestrating the activity of multiple transcription factors, p38 MAPK is a central mediator of the cAMP signaling mechanism of brown fat that promotes thermogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / metabolism
  • Adipose Tissue, Brown / physiology*
  • Animals
  • Carrier Proteins / genetics*
  • Cells, Cultured
  • Cold Temperature
  • Cyclic AMP / metabolism*
  • Enhancer Elements, Genetic
  • Enzyme Activation
  • Enzyme Inhibitors / metabolism
  • Gene Expression Regulation*
  • Humans
  • Ion Channels
  • Membrane Proteins / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mitochondrial Proteins
  • Mitogen-Activated Protein Kinases / metabolism*
  • Random Allocation
  • Signal Transduction / physiology
  • Thermogenesis / physiology
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic*
  • Uncoupling Agents
  • Uncoupling Protein 1
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Carrier Proteins
  • Enzyme Inhibitors
  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • Transcription Factors
  • UCP1 protein, human
  • Ucp1 protein, mouse
  • Uncoupling Agents
  • Uncoupling Protein 1
  • peroxisome-proliferator-activated receptor-gamma coactivator-1
  • Cyclic AMP
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases