Suppression of mitochondrial respiration through recruitment of p160 myb binding protein to PGC-1alpha: modulation by p38 MAPK

Genes Dev. 2004 Feb 1;18(3):278-89. doi: 10.1101/gad.1152204. Epub 2004 Jan 26.

Abstract

The transcriptional coactivator PPAR gamma coactivator 1 alpha (PGC-1alpha) is a key regulator of metabolic processes such as mitochondrial biogenesis and respiration in muscle and gluconeogenesis in liver. Reduced levels of PGC-1alpha in humans have been associated with type II diabetes. PGC-1alpha contains a negative regulatory domain that attenuates its transcriptional activity. This negative regulation is removed by phosphorylation of PGC-1alpha by p38 MAPK, an important kinase downstream of cytokine signaling in muscle and beta-adrenergic signaling in brown fat. We describe here the identification of p160 myb binding protein (p160MBP) as a repressor of PGC-1alpha. The binding and repression of PGC-1alpha by p160MBP is disrupted by p38 MAPK phosphorylation of PGC-1alpha. Adenoviral expression of p160MBP in myoblasts strongly reduces PGC-1alpha's ability to stimulate mitochondrial respiration and the expression of the genes of the electron transport system. This repression does not require removal of PGC-1alpha from chromatin, suggesting that p160MBP is or recruits a direct transcriptional suppressor. Overall, these data indicate that p160MBP is a powerful negative regulator of PGC-1alpha function and provide a molecular mechanism for the activation of PGC-1alpha by p38 MAPK. The discovery of p160MBP as a PGC-1alpha regulator has important implications for the understanding of energy balance and diabetes.

Publication types

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

MeSH terms

  • Animals
  • Carrier Proteins / metabolism
  • Carrier Proteins / pharmacology*
  • Cell Respiration*
  • Cells, Cultured
  • DNA-Binding Proteins
  • Energy Metabolism
  • Gene Expression Regulation
  • MAP Kinase Signaling System
  • Mitochondria, Muscle / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Muscle, Skeletal / metabolism
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / pharmacology*
  • Nucleocytoplasmic Transport Proteins
  • RNA-Binding Proteins
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Repressor Proteins / pharmacology*
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Transfection
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Carrier Proteins
  • DNA-Binding Proteins
  • MYBBP1A protein, human
  • Nuclear Proteins
  • Nucleocytoplasmic Transport Proteins
  • RNA-Binding Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Repressor Proteins
  • Transcription Factors
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases