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J Biol Chem. 2008 Mar 28;283(13):8070-4. doi: 10.1074/jbc.C700221200. Epub 2008 Feb 5.

Deregulated protein kinase A signaling and myospryn expression in muscular dystrophy.

Author information

1
Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, MA 02215, USA.

Abstract

Alterations in signaling pathway activity have been implicated in the pathogenesis of Duchenne muscular dystrophy, a degenerative muscle disease caused by a deficiency in the costameric protein dystrophin. Accordingly, the notion of the dystrophin-glycoprotein complex, and by extension the costamere, as harboring signaling components has received increased attention in recent years. The localization of most, if not all, signaling enzymes to this subcellular region relies on interactions with scaffolding proteins directly or indirectly associated with the dystrophin-glycoprotein complex. One of these scaffolds is myospryn, a large, muscle-specific protein kinase A (PKA) anchoring protein or AKAP. Previous studies have demonstrated a dysregulation of myospryn expression in human Duchenne muscular dystrophy, suggesting a connection to the pathophysiology of the disorder. Here we report that dystrophic muscle exhibits reduced PKA activity resulting, in part, from severely mislocalized myospryn and the type II regulatory subunit (RIIalpha) of PKA. Furthermore, we show that myospryn and dystrophin coimmunoprecipitate in native muscle extracts and directly interact in vitro. Our findings reveal for the first time abnormalities in the PKA signal transduction pathway and myospryn regulation in dystrophin deficiency.

PMID:
18252718
PMCID:
PMC2276392
DOI:
10.1074/jbc.C700221200
[Indexed for MEDLINE]
Free PMC Article
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