4.8 Article

The transcriptional coactivator PGC-1β drives the formation of oxidative type IIX fibers in skeletal muscle

Journal

CELL METABOLISM
Volume 5, Issue 1, Pages 35-46

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2006.12.003

Keywords

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Funding

  1. NHLBI NIH HHS [HL079172] Funding Source: Medline
  2. NIDDK NIH HHS [R01 DK054477, DK61562, DK54477] Funding Source: Medline

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Skeletal muscle must perform different kinds of work, and distinct fiber types have evolved to accommodate these. Previous work had shown that the transcriptional coactivator PGC-1 alpha drives the formation of type I and IIA muscle fibers, which are slow-twitch and highly oxidative. We show here that transgenic expression of PGC-1 beta, a coactivator functionally similar to but distinct from PGC-1 alpha, causes a marked induction of IN fibers, which are oxidative but have fast-twitch biophysical properties. PGC-1 beta coactivates the MEF2 family of transcription factors to stimulate the type IIX myosin heavy chain (MHC) promoter. PGC-1 beta transgenic muscle fibers are rich in mitochondria and are highly oxidative, at least in part due to coactivation by PGC-1 beta of ERR alpha and PPAR alpha. Consequently, these transgenic animals can run for longer and at higher work loads than wild-type animals. Together, these data indicate that PGC-1 beta drives the formation of highly oxidative fibers containing type IIX MHC.

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