共 50 条
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.
引用
收藏
页码:S243 / S248
页数:6
相关论文