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Sterol Regulatory Element Binding Protein-1c Expression and Action in Rat Muscles: Insulin-Like Effects on the Control of Glycolytic and Lipogenic Enzymes and UCP3 Gene Expression

  1. Isabelle Guillet-Deniau1,
  2. Virginie Mieulet1,
  3. Soazig Le Lay2,
  4. Younes Achouri2,
  5. Denis Carré1,
  6. Jean Girard1,
  7. Fabienne Foufelle2 and
  8. Pascal Ferré2
  1. 1UPR 1524 CNRS, Institut Cochin de Génétique Moléculaire, Paris, France
  2. 2Unité INSERM 465, Centre de Recherches Biomédicales des Cordeliers, Université Paris VI, Paris, France

    Abstract

    Sterol regulatory element binding protein-1c (SREBP-1c) is a transcription factor that mediates insulin effects on hepatic gene expression. It is itself transcriptionally stimulated by insulin in hepatocytes. Here we show that SREBP-1c mRNA is expressed in adult rat skeletal muscles and that this expression is decreased by diabetes. The regulation of SREBP-1c expression was then assessed in cultures of adult muscle satellite cells. These cells form spontaneously contracting multinucleated myotubes within 7 days of culture. SREBP-1c mRNA is expressed in contracting myotubes. A 4-h treatment with 100 nmol/l insulin increases SREBP-1c expression and nuclear abundance by two- to threefold in myotubes. In cultured myotubes, insulin increases the expression of glycolytic and lipogenic enzyme genes and inhibits the 9-cis retinoic acid-induced UCP3 expression. These effects of insulin are mimicked by adenovirus-mediated expression of a transcriptionally active form of SREBP-1c. We conclude that in skeletal muscles, SREBP-1c expression is sensitive to insulin and can transduce the positive and negative actions of the hormone on specific genes and thus has a pivotal role in long-term muscle insulin sensitivity.

    Footnotes

    • Address correspondence and reprint requests to Isabelle Guillet-Deniau, Institut Cochin de Génétique Moléculaire, 24 rue du Faubourg St-Jacques, 75014, Paris, France. E-mail: guillet-deniau{at}cochin.inserm.fr.

      Received for publication 14 August 2001 and accepted in revised form 27 February 2002.

      EDL, extensor digitorum longus; FAS, fatty acid synthase; HK, hexokinase; PPAR, peroxisome proliferator-activated receptor; SREBP, sterol regulatory element binding protein; STZ, streptozotocin.

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