Published 2 September 2003. doi:10.1083/jcb.200303164
© The Rockefeller University Press,
0021-9525/2003/9/843 $5.00
The Journal of Cell Biology, Volume 162, Number 5, 843-850
Repression of slow myosin heavy chain 2 gene expression in fast skeletal muscle fibers by muscarinic acetylcholine receptor and G
q signaling
Theresa Jordan,
Jinyuan Li,
Hongbin Jiang and
Joseph X. DiMario
Department of Cell Biology and Anatomy, Chicago Medical School, North Chicago, IL 60064
Address correspondence to Joseph X. DiMario, Dept. of Cell Biology and Anatomy, Chicago Medical School, 3333 Green Bay Rd., North Chicago, IL 60064. Tel: (847) 578-8633. Fax: (847) 578-3253. email: dimarioj{at}finchcms.edu
Gene expression in skeletal muscle fibers is regulated by innervation and intrinsic fiber properties. To determine the mechanism of repression of slow MyHC2 expression in innervated fast pectoralis major (PM) fibers, we investigated the function of the muscarinic acetylcholine receptor (mAchR) and G
q. Both mAchR and G
q are abundant in medial adductor (MA) and PM fibers, and mAchR and G
q interact in these fibers. Whereas innervation of PM fibers was insufficient to induce slow MyHC2 expression, inhibition of mAchR activity with atropine in innervated PM fibers induced slow MyHC2 expression. Increased G
q activity repressed slow MyHC2 expression to nondetectable levels in innervated MA fibers. Reduced mAchR activity decreased PKC activity in PM fibers, and increased G
q activity increased PKC activity in PM and MA fibers. Decreased PKC activity in atropine-treated innervated PM fibers correlated with slow MyHC2 expression. These data suggest that slow MyHC2 repression in innervated fast PM fibers is mediated by cell signaling involving mAchRs, G
q, and PKC.
Key Words: mAchR; innervation; fiber type; MyHC; PKC
Abbreviations used in this paper: DAG, diacylglycerol; ED, embryonic day; IP3, inositol triphosphate; MA, medial adductor; mAchR, muscarinic acetylcholine receptor; MyHC, myosin heavy chain; nAchR, nicotinic AchR; PM, pectoralis major.

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