Abstract
SREBP-1 are ubiquitously expressed transcription factors, strongly expressed in lipogenic tissues where they regulate several metabolic processes like fatty acid synthesis. In skeletal muscle, SREBP-1 proteins regulate the expression of hundreds of genes, and we previously showed that their overexpression induced muscle atrophy together with a combined lack of expression of myogenic regulatory factors. Here we present evidences that SREBP-1 regulate muscle protein synthesis through the downregulation of the expression of MYOD1, MYOG and MEF2C factors. In myotubes overexpressing SREBP-1, restoring the expression of myogenic factors prevented atrophy and rescued protein synthesis, without affecting SREBP-1 action on atrogenes and proteolysis. Our results point out the roles of MRFs in the maintenance of the protein content and cell size in adult muscle fibre, and contribute to decipher the mechanisms by which SREBP-1 regulate muscle mass.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell Size*
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Humans
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MADS Domain Proteins / metabolism
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MEF2 Transcription Factors
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Muscle Fibers, Skeletal / metabolism
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Muscle Fibers, Skeletal / pathology
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Muscle, Skeletal / pathology*
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MyoD Protein / metabolism
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Myogenic Regulatory Factors / metabolism*
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Myogenin / metabolism
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Protein Biosynthesis*
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Proteolysis
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RNA, Small Interfering / metabolism
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Sarcomeres / metabolism
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Sterol Regulatory Element Binding Protein 1 / metabolism*
Substances
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MADS Domain Proteins
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MEF2 Transcription Factors
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MEF2C protein, human
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MYOG protein, human
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MyoD Protein
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MyoD1 myogenic differentiation protein
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Myogenic Regulatory Factors
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Myogenin
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RNA, Small Interfering
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SREBF1 protein, human
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Sterol Regulatory Element Binding Protein 1
Grants and funding
This work was supported by INSERM, INRA, and a grant from the Cancéropôle Lyon Rhône-Alpes (Procan Axe III 2010). KD and JDL are recipients of PhD fellowships from the French Ministry of Higher Education. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.