科研之友
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摘要
PGC-1 alpha is a transcriptional coactivator promoting oxidative metabolism in many tissues. Its expression in skeletal muscle (SKM) is induced by hypoxia and reactive oxidative species (ROS) generated during exercise, suggesting that PGC-1 alpha might mediate the cross talk between oxidative metabolism and cellular responses to hypoxia and ROS. Here we found that PGC-1 alpha directly interacted with Bhlhe40, a basic helix-loop-helix (bHLH) transcriptional repressor induced by hypoxia, and protects SKM from ROS damage, and they cooccupied PGC-1 alpha-targeted gene promoters/enhancers, which in turn repressed PGC-1 alpha transactivational activity. Bhlhe40 repressed PGC-1 alpha activity through recruiting histone deacetylases (HDACs) and preventing the relief of PGC-1 alpha intramolecular repression caused by its own intrinsic suppressor domain. Knockdown of Bhlhe40 mRNA increased levels of ROS, fatty acid oxidation, mitochondrial DNA, and expression of PGC-1 alpha target genes. Similar effects were also observed when the Bhlhe40-mediated repression was rescued by a dominantly active form of the PGC-1 alpha-interacting domain (PID) from Bhlhe40. We further found that Bhlhe40-mediated repression can be largely relieved by exercise, in which its recruitment to PGC-1 alpha-targeted cis elements was significantly reduced. These observations suggest that Bhlhe40 is a novel regulator of PGC-1 alpha activity repressing oxidative metabolism gene expression and mitochondrion biogenesis in sedentary SKM.
- 出版日期2015-7
- 单位中央民族大学
