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Molecular and Cellular Biology, May 2008, p. 2952-2970, Vol. 28, No. 9
0270-7306/08/$08.00+0     doi:10.1128/MCB.00248-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Protein Kinase A Represses Skeletal Myogenesis by Targeting Myocyte Enhancer Factor 2D ^,

Min Du,^1,2 Robert L. S. Perry,¹ Nathaniel B. Nowacki,¹ Joseph W. Gordon,¹ Jahan Salma,¹ Jianzhong Zhao,¹ Arif Aziz,¹ Joseph Chan,¹ K. W. Michael Siu,^1,2,3 and John C. McDermott^1,2*

Department of Biology, York University, Toronto M3J 1P3, Ontario, Canada,¹ Centre for Research in Mass Spectrometry, York University, Toronto M3J 1P3, Ontario, Canada,² Department of Chemistry, York University, Toronto M3J 1P3, Ontario, Canada³

Received 14 February 2008/ Accepted 19 February 2008

Activation of protein kinase A (PKA) by elevation of the intracellular cyclic AMP (cAMP) level inhibits skeletal myogenesis. Previously, an indirect modulation of the myogenic regulatory factors (MRFs) was implicated as the mechanism. Because myocyte enhancer factor 2 (MEF2) proteins are key regulators of myogenesis and obligatory partners for the MRFs, here we assessed whether these proteins could be involved in PKA-mediated myogenic repression. Initially, in silico analysis revealed several consensus PKA phosphoacceptor sites on MEF2, and subsequent analysis by in vitro kinase assays indicated that PKA directly and efficiently phosphorylates MEF2D. Using mass spectrometric determination of phosphorylated residues, we document that MEF2D serine 121 and serine 190 are targeted by PKA. Transcriptional reporter gene assays to assess MEF2D function revealed that PKA potently represses the transactivation properties of MEF2D. Furthermore, engineered mutation of MEF2D PKA phosphoacceptor sites (serines 121 and 190 to alanine) rendered a PKA-resistant MEF2D protein, which efficiently rescues myogenesis from PKA-mediated repression. Concomitantly, increased intracellular cAMP-mediated PKA activation also resulted in an enhanced nuclear accumulation of histone deacetylase 4 (HDAC4) and a subsequent increase in the MEF2D-HDAC4 repressor complex. Collectively, these data identify MEF2D as a primary target of PKA signaling in myoblasts that leads to inhibition of the skeletal muscle differentiation program.

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* Corresponding author. Mailing address: Department of Biology, York University, 4700 Keele Street, Toronto M3J 1P3, Ontario, Canada. Phone: (416) 736-2100, ext. 30389. Fax: (416) 736-5698. E-mail: jmcderm{at}yorku.ca

Published ahead of print on 25 February 2008.

Supplemental material for this article may be found at http://mcb.asm.org/.

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Molecular and Cellular Biology, May 2008, p. 2952-2970, Vol. 28, No. 9
0270-7306/08/$08.00+0     doi:10.1128/MCB.00248-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

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