Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2

Osamu Nakagawa(Southwestern Medical Center), Michael Arnold(Howard Hughes Medical Institute), Masayo Nakagawa(Howard Hughes Medical Institute), Hideaki Hamada(Howard Hughes Medical Institute), John M. Shelton(Howard Hughes Medical Institute), Hajime Kusano(University of Iowa), Thomas M. Harris(Albert Einstein College of Medicine), Geoffrey Childs(Albert Einstein College of Medicine), Kevin P. Campbell(University of Iowa), James A. Richardson(Howard Hughes Medical Institute), Ichizo Nishino(Howard Hughes Medical Institute), Eric N. Olson(Howard Hughes Medical Institute)
Genes & Development
September 1, 2005
Cited by 124Open Access
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Abstract

Myocyte enhancer factor 2 (MEF2) plays essential roles in transcriptional control of muscle development. However, signaling pathways acting downstream of MEF2 are largely unknown. Here, we performed a microarray analysis using Mef2c-null mouse embryos and identified a novel MEF2-regulated gene encoding a muscle-specific protein kinase, Srpk3, belonging to the serine arginine protein kinase (SRPK) family, which phosphorylates serine/arginine repeat-containing proteins. The Srpk3 gene is specifically expressed in the heart and skeletal muscle from embryogenesis to adulthood and is controlled by a muscle-specific enhancer directly regulated by MEF2. Srpk3-null mice display a new entity of type 2 fiber-specific myopathy with a marked increase in centrally placed nuclei; while transgenic mice overexpressing Srpk3 in skeletal muscle show severe myofiber degeneration and early lethality. We conclude that normal muscle growth and homeostasis require MEF2-dependent signaling by Srpk3.


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