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pubmed-article:10543731pubmed:abstractTextSM-20 is a novel, evolutionarily conserved "early response" gene originally cloned from a rat aortic smooth muscle cell (SMC) cDNA library. SM-20 encodes a cytoplasmic protein, which is induced by platelet-derived growth factor and angiotensin II in cultured SMC and is upregulated in intimal SMC of atherosclerotic plaques and injured arteries. We have now examined SM-20 expression during differentiation of cultured skeletal myoblasts and during skeletal myogenesis in vivo. Low levels of SM-20 mRNA and protein were expressed in proliferating mouse C2C12 myoblasts. Differentiation by serum withdrawal was associated with a marked induction of SM-20 mRNA and the expression of high levels of SM-20 antigen in myotubes. The induction was partially inhibited by blocking differentiation with bFGF or TGFbeta. Similar results were obtained with the nonfusing mouse C25 myoblast line, suggesting that SM-20 upregulation is a consequence of biochemical differentiation and is fusion independent. During mouse embryogenesis, SM-20 was first observed at 8.5E in the dermomyotomal cells of the rostral somites. SM-20 expression progressed in a rostral to caudal pattern, with highest levels seen in the muscle primordia and mature muscles. SM-20 thus represents a novel intracellular protein that is regulated during skeletal muscle differentiation and development.lld:pubmed
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pubmed-article:10543731pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:10543731pubmed:articleTitleSM-20 is a novel growth factor-responsive gene regulated during skeletal muscle development and differentiation.lld:pubmed
pubmed-article:10543731pubmed:affiliationThe Michael A. and Zena Wiener Cardiovascular Institute, Department of Medicine, The Mount Sinai School of Medicine, New York, NY 10029, USA.lld:pubmed
pubmed-article:10543731pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10543731pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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