PAK4, a novel effector for Cdc42Hs, is implicated in the reorganization of the actin cytoskeleton and in the formation of filopodia

被引:313
作者
Abo, A
Qu, J
Cammarano, MS
Dan, CT
Fritsch, A
Baud, V
Belisle, B
Minden, A
机构
[1] Onyx Pharmaceut, Richmond, CA 94806 USA
[2] Columbia Univ, Biol Sci MC 2460, Sherman Fairchild Ctr, New York, NY 10027 USA
[3] Univ Calif San Diego, Sch Med, Dept Pharmacol, La Jolla, CA 92093 USA
关键词
Cdc42Hs; cytoskeleton; filopodia; PAK;
D O I
10.1093/emboj/17.22.6527
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 GTPases Rac and Cdc42Hs control diverse cellular functions. In addition to being mediators of intracellular signaling cascades, they have important roles in cell morphogenesis and mitogenesis. We have identified a novel PAK-related kinase, PAK4, as a new effector molecule for Cdc42Hs. PAK4 interacts only with the activated form of Gdc42Hs through its GTPase-binding domain (GBD). Go-expression of PAK4 and the constitutively active Cdc42HsV12 causes the redistribution of PAK4 to the brefeldin A-sensitive compartment of the Golgi membrane and the subsequent induction of filopodia and actin polymerization. Importantly, the reorganization of the actin cytoskeleton is dependent on PAK4 kinase activity and on its interaction with Cdc42Hs. Thus, unlike other members of the PAK family, PAK4 provides a novel link between Cdc42Hs and the actin cytoskeleton. The cellular locations of PAK4 and Cdc42Hs suggest a role for the Golgi in cell morphogenesis.
引用
收藏
页码:6527 / 6540
页数:14
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