Comparative functional analysis of the Rac GTPases

被引:67
作者
Haeusler, LC [1 ]
Blumenstein, L [1 ]
Stege, P [1 ]
Dvorsky, R [1 ]
Ahmadian, MR [1 ]
机构
[1] Max Planck Inst Mol Physiol, Dept Biol Struct, D-44227 Dortmund, Germany
关键词
Rac1; Rac2; Rac3; Rae isoform; T-lymphoma invasion and metastasis; GTPase;
D O I
10.1016/S0014-5793(03)01351-6
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
Small GTPases of the Rho family including Rac, Rho and Cdc42 regulate different cellular processes like reorganization of the actin cytoskeleton by acting as molecular switches. The three distinct mammalian Rac proteins share very high sequence identity but how their specificity is achieved is hitherto unknown. Here we show that Rac1 and Rac3 are very closely related concerning their biochemical properties, such as effector interaction, nucleotide binding and hydrolysis. In contrast, Rac2 displays a slower nucleotide association and is more efficiently activated by the Rac-GEF Tiam1. Modeling and normal mode analysis support the idea that altered dynamics of Rac2 at the switch I region may be responsible for different biochemical properties. These results provide insight into the individual functionalities of the Rac isoforms. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:556 / 560
页数:5
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