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Originally published In Press as doi:10.1074/jbc.M203680200 on May 31, 2002

J. Biol. Chem., Vol. 277, Issue 32, 28742-28748, August 9, 2002
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Inhibition of myogenin Expression by Activated Raf Is Not Responsible for the Block to Avian Myogenesis*

Sally E. JohnsonDagger , Christine M. Dorman, and Stacey A. Bolanowski

From the Department of Poultry Science, The Pennsylvania State University, University Park, Pennsylvania 16802

Activated Raf is a potent inhibitor of skeletal muscle gene transcription and myocyte formation through stimulation of downstream MAPK. However, the molecular targets of elevated MAPK with regard to myogenic repression remain elusive. We examined the effects of activated Raf on myogenin gene expression in avian myoblasts. Overexpression of activated Raf in embryonic chick myoblasts prevented myogenin gene transcription and myocyte differentiation. Treatment with PD98059, an inhibitor of MAPK kinase (MEK), restored myogenin expression but did not reinstate the myogenic program. Using a panel of myogenin promoter deletion mutants, we were unable to identify a region within the proximal 829-bp promoter that confers responsiveness to MEK. Interestingly, our experiments identified MEF2A as a target of Raf-mediated inhibition in mouse myoblasts but not in avian myogenic cells. Embryonic myoblasts overexpressing activated Raf were unable to drive transcription from a minimal myogenin promoter reporter, containing a single E-box and MEF2 site, to levels comparable with controls. Unlike mouse myoblasts, forced expression of MEF2A did not synergistically enhance transcription from the myogenin promoter in chick myoblasts, indicating that additional molecular determinants of the block to myogenesis exist. Results of these experiments further exemplify specie differences in the mode of Raf-mediated inhibition of muscle differentiation.


* This work was supported by Grant RPG-00-253-01-DDC from the American Cancer Society (to S. E. J.) and Grant NRICGP 9803668 from the United States Department of Agriculture (to S. E. J.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence should be addressed: The Pennsylvania State University, Dept. of Poultry Science, 206 Henning, University Park, PA 16802. Tel.: 814-863-2137; Fax: 814-865-5691; E-mail: sej4@psu.edu.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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