Phospholipase C isozymes as effectors of Ras superfamily GTPases

被引:33
|
作者
Harden, T. Kendall [1 ,2 ]
Hicks, Stephanie N. [1 ]
Sondek, John [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Dept Pharmacol, Sch Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Sch Med, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
inositol lipid signaling; Rac; Rho; Rap; PLECKSTRIN HOMOLOGY DOMAIN; G-PROTEINS; DEPENDENT ACTIVATION; CRYSTAL-STRUCTURE; CRUCIAL ROLE; RHO GTPASES; EPSILON; STIMULATION; C-BETA(2); SITE;
D O I
10.1194/jlr.R800045-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The physiological effects of many extracellular stimuli are initiated through receptor-promoted activation of phospholipase C and inositol lipid signaling pathways. The historical view that phospholipase C-promoted signaling primarily occurs through activation of heterotrimeric G proteins or tyrosine kinases has expanded in recent years with the realization that at least three different mammalian phospholipase C isozymes are directly activated by members of the Ras superfamily of GTPases. jlr Thus, Ras, Rap, Rac, and Rho GTPases all specifically regulate certain phospholipase C isozymes, and insight into the physiological significance of these signaling responses is beginning to accrue. High resolution three-dimensional structures of phospholipase C isozymes also are beginning to shed light on their mechanism of activation.-Harden, T. K., S. N. Hicks, and J. Sondek. Phospholipase C isozymes as effectors of Ras superfamily GTPases. J. Lipid Res. 2009. S243-S248.
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页码:S243 / S248
页数:6
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