Rac1 and Cdc42 capture microtubules through IQGAP1 and CLIP-170

被引:497
作者
Fukata, M
Watanabe, T
Noritake, J
Nakagawa, M
Yamaga, M
Kuroda, S
Matsuura, Y
Iwamatsu, A
Perez, F
Kaibuchi, K
机构
[1] Nagoya Univ, Grad Sch Med, Dept Cell Pharmacol, Showa Ku, Aichi 4668550, Japan
[2] Nara Inst Sci & Technol, Div Signal Transduct, Nara 6300101, Japan
[3] Osaka Univ, Res Ctr Emerging Infect Dis, Suita, Osaka 5650871, Japan
[4] Kirin Brewery Co Ltd, Cent Labs Key Technol, Kanagawa 2360004, Japan
[5] Inst Curie, CNRS, UMR 144, Paris 05, France
基金
日本学术振兴会;
关键词
D O I
10.1016/S0092-8674(02)00800-0
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
Linkage of microtubules to special cortical regions is essential for cell polarization. CLIP-170 binds to the growing ends of microtubules and plays pivotal roles in orientation. We have found that IQGAP1, an effector of Rac1 and Cdc42, interacts with CLIP-170. In Vero fibroblasts, IQGAP1 localizes at the polarized leading edge. Expression of carboxy-terminal fragment of 1Q-GAP1, which includes the CLIP-170 binding region, delocalizes GFP-CLIP-170 from the tips of microtubules and alters the microtubule array. Activated Rac1/Cdc42, IQGAP1, and CLIP-170 form a tripartite complex. Furthermore, expression of an IQGAP1 mutant defective in Rac1/Cdc42 binding induces multiple leading edges. These results indicate that Rac1/Cdc42 marks special cortical spots where the IQGAP1 and CLIP-170 complex is targeted, leading to a polarized microtubule array and cell polarization.
引用
收藏
页码:873 / 885
页数:13
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