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

Abstract

The transcriptional coactivator PPAR gamma coactivator 1 α (PGC-1α) is a key regulator of metabolic processes such as mitochondrial biogenesis and respiration in muscle and gluconeogenesis in liver. Reduced levels of PGC-1α in humans have been associated with type II diabetes. PGC-1α contains a negative regulatory domain that attenuates its transcriptional activity. This negative regulation is removed by phosphorylation of PGC-1α by p38 MAPK, an important kinase downstream of cytokine signaling in muscle and β-adrenergic signaling in brown fat. We describe here the identification of p160 myb binding protein (p160^MBP) as a repressor of PGC-1α. The binding and repression of PGC-1α by p160^MBP is disrupted by p38 MAPK phosphorylation of PGC-1α. Adenoviral expression of p160^MBP in myoblasts strongly reduces PGC-1α'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-1α from chromatin, suggesting that p160^MBP is or recruits a direct transcriptional suppressor. Overall, these data indicate that p160^MBP is a powerful negative regulator of PGC-1α function and provide a molecular mechanism for the activation of PGC-1α by p38 MAPK. The discovery of p160^MBP as a PGC-1α regulator has important implications for the understanding of energy balance and diabetes.

Keywords

• PGC-1α
• Mybbp1a
• mitochondria
• repressor
• p38 MAPK