JunB Transcription Factor Maintains Skeletal Muscle Mass and Promotes Hypertrophy

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JunB Transcription Factor Maintains Skeletal Muscle Mass and Promotes Hypertrophy

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Title: JunB Transcription Factor Maintains Skeletal Muscle Mass and Promotes Hypertrophy
Author: Raffaello, Anna; Milan, Giulia; Masiero, Eva; Carnio, Silvia; Lanfranchi, Gerolamo; Sandri, Marco; Goldberg, Alfred L.; Lee, Dong-Hoon

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Citation: Raffaello, Anna, Giulia Milan, Eva Masiero, Silvia Carnio, Dong-Hoon Lee, Gerolamo Lanfranchi, Alfred Lewis Goldberg, and Marco Sandri. 2010. JunB transcription factor maintains skeletal muscle mass and promotes hypertrophy. The Journal of Cell Biology 191(1): 101-113.
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Abstract: The size of skeletal muscle cells is precisely regulated by intracellular signaling networks that determine the balance between overall rates of protein synthesis and degradation. Myofiber growth and protein synthesis are stimulated by the IGF-1/Akt/mammalian target of rapamycin (mTOR) pathway. In this study, we show that the transcription factor JunB is also a major determinant of whether adult muscles grow or atrophy. We found that in atrophying myotubes, JunB is excluded from the nucleus and that decreasing JunB expression by RNA interference in adult muscles causes atrophy. Furthermore, JunB overexpression induces hypertrophy without affecting satellite cell proliferation and stimulated protein synthesis independently of the Akt/mTOR pathway. When JunB is transfected into denervated muscles, fiber atrophy is prevented. JunB blocks FoxO3 binding to atrogin-1 and MuRF-1 promoters and thus reduces protein breakdown. Therefore, JunB is important not only in dividing populations but also in adult muscle, where it is required for the maintenance of muscle size and can induce rapid hypertrophy and block atrophy.
Published Version: doi://10.1083/jcb.201001136
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953439/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:7351760

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