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与IQGAP相关的蛋白质DGAP1与Rac相互作用,参与F-肌动蛋白细胞骨架的调节和细胞运动的控制。

The IQGAP-related protein DGAP1 interacts with Rac and is involved in the modulation of the F-actin cytoskeleton and control of cell motility.

作者信息

Faix J, Clougherty C, Konzok A, Mintert U, Murphy J, Albrecht R, Mühlbauer B, Kuhlmann J

机构信息

Max-Planck-Institut für Biochemie, D-82152 Martinsried, Germany.

出版信息

J Cell Sci. 1998 Oct;111 ( Pt 20):3059-71. doi: 10.1242/jcs.111.20.3059.

DOI:10.1242/jcs.111.20.3059
PMID:9739079
Abstract

DGAP1 of Dictyostelium discoideum is a cell cortex associated 95 kDa protein that shows homology to both RasGTPase-activating proteins (RasGAPs) and RasGAP-related proteins. When tested for RasGAP activity, recombinant DGAP1 protein did not promote the GTPase activity of human H-Ras or of Dictyostelium RasG in vitro. Instead, DGAP1 bound to Dictyostelium Rac1A and human Rac1, but not to human Cdc42. DGAP1 preferentially interacted with the activated GTP-bound forms of Rac1 and Rac1A, but did not affect the GTPase activities. Since Rho-type GTPases are implicated in the formation of specific F-actin structures and in the control of cell morphology, the microfilament system of mutants that either lack or overexpress DGAP1 has been analysed. DGAP1-null mutants showed elevated levels of F-actin that was organised in large leading edges, membrane ruffles or numerous large filopods. Expression of actin fused to green fluorescent protein (GFP) was used to monitor the actin dynamics in these cells, and revealed that the F-actin cytoskeleton of DGAP1-null cells was rapidly re-arranged to form ruffles and filopods. Conversely, in DGAP1-overexpressing cells, the formation of cellular projections containing F-actin was largely suppressed. Measurement of cell migration demonstrated that DGAP1 expression is inversely correlated with the speed of cell motility.

摘要

盘基网柄菌的DGAP1是一种与细胞皮层相关的95 kDa蛋白,与RasGTP酶激活蛋白(RasGAPs)和RasGAP相关蛋白均具有同源性。在检测其RasGAP活性时,重组DGAP1蛋白在体外并未促进人H-Ras或盘基网柄菌RasG的GTP酶活性。相反,DGAP1与盘基网柄菌Rac1A和人Rac1结合,但不与人Cdc42结合。DGAP1优先与Rac1和Rac1A的活化GTP结合形式相互作用,但不影响GTP酶活性。由于Rho型GTP酶与特定F-肌动蛋白结构的形成及细胞形态的控制有关,因此对缺乏或过表达DGAP1的突变体的微丝系统进行了分析。DGAP1基因缺失突变体显示F-肌动蛋白水平升高,这些F-肌动蛋白组织成大的前缘、膜皱褶或众多大的丝状伪足。利用与绿色荧光蛋白(GFP)融合的肌动蛋白的表达来监测这些细胞中的肌动蛋白动态,结果显示DGAP1基因缺失细胞的F-肌动蛋白细胞骨架迅速重新排列形成皱褶和丝状伪足。相反,在过表达DGAP1的细胞中,含有F-肌动蛋白的细胞突起的形成受到很大抑制。细胞迁移的测量表明,DGAP1的表达与细胞运动速度呈负相关。

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