Why three Rho proteins? RhoA, RhoB, RhoC, and cell motility

被引:387
作者
Wheeler, AP
Ridley, AJ
机构
[1] Royal Free & Univ Coll Med Sch, Sch Med, Ludwig Inst Canc Res, Lab Cell Mol Biol, London W1W 7BS, England
[2] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[3] UCL, MRC, Cell Biol Unit, London WC1E 6BT, England
[4] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
关键词
vertebrate; isoform; protein;
D O I
10.1016/j.yexcr.2004.08.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Higher vertebrates have 3 Rho GTPases, RhoA, RhoB, and RhoC, which share 85% amino acid sequence identity. Here, we compare and contrast the roles of RhoA, B, and C in the regulation of the cytoskeleton and cell motility. Despite their similarity, some regulators and effectors show preferential interaction with RhoA, B, or C, and the three proteins show differences in function in cells. RhoA plays a key role in the regulation of actomyosin contractility. RhoB, which is localized primarily on endosomes, has been shown to regulate cytokine trafficking and cell survival, while RhoC may be more important in cell locomotion. In cancer cells, the expression and activity of RhoA, B, and C is altered in different ways. Together, this evidence suggests that although the 3 isoforms of Rho are structurally highly homologous, they have different cellular functions. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 45 条
[1]   INTRACELLULAR-LOCALIZATION OF THE P21(RHO) PROTEINS [J].
ADAMSON, P ;
PATERSON, HF ;
HALL, A .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :617-627
[2]   RhoB controls Akt trafficking and stage-specific survival of endothelial cells during vascular development [J].
Adini, I ;
Rabinovitz, I ;
Sun, JF ;
Prendergast, GC ;
Benjamin, LE .
GENES & DEVELOPMENT, 2003, 17 (21) :2721-2732
[3]   RhoB, not RhoA, represses the transcription of the transforming growth factor β type II receptor by a mechanism involving activator protein 1 [J].
Adnane, J ;
Seijo, E ;
Chen, Z ;
Bizouarn, F ;
Leal, M ;
Sebti, SM ;
Muñoz-Antonia, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8500-8507
[4]   RhoA prenylation is required for promotion of cell growth and transformation and cytoskeleton organization but not for induction of serum response element transcription [J].
Allal, C ;
Favre, G ;
Couderc, B ;
Salicio, S ;
Sixou, S ;
Hamilton, AD ;
Sebti, SM ;
Lajoie-Mazenc, I ;
Pradines, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) :31001-31008
[5]   Farnesylated RhoB Prevents Cell Cycle Arrest and Actin Cytoskeleton Disruption Caused by the Geranylgeranyltransferase I Inhibitor GGTI-298 [J].
Allal, Cuider ;
Pradines, Anne ;
Hamilton, Andrew D. ;
Sebti, Said M. ;
Favre, Gilles .
CELL CYCLE, 2002, 1 (06) :430-437
[6]   XPLN, a guanine nucleotide exchange factor for RhoA and RhoB, but not RhoC [J].
Arthur, WT ;
Ellerbroek, SM ;
Der, CJ ;
Burridge, K ;
Wennerberg, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) :42964-42972
[7]   Characterization of Gα13-dependent plasma membrane recruitment of p115RhoGEF [J].
Bhattacharyya, R ;
Wedegaertner, PB .
BIOCHEMICAL JOURNAL, 2003, 371 :709-720
[8]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255
[9]   Rho and Rac take center stage [J].
Burridge, K ;
Wennerberg, K .
CELL, 2004, 116 (02) :167-179
[10]   CHROMOSOME LOCALIZATION OF HUMAN ARH GENES, A RAS-RELATED GENE FAMILY [J].
CANNIZZARO, LA ;
MADAULE, P ;
HECHT, F ;
AXEL, R ;
CROCE, CM ;
HUEBNER, K .
GENOMICS, 1990, 6 (02) :197-203