How Vav proteins discriminate the GTPases Rac1 and RhoA from Cdc42

被引:59
作者
Movilla, N
Dosil, M
Zheng, Y
Bustelo, XR [1 ]
机构
[1] Univ Salamanca, CSIC, Ctr Invest Canc, Salamanca 37007, Spain
[2] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, Salamanca 37007, Spain
[3] Univ Tennessee, Dept Mol Sci, Memphis, TN 38163 USA
[4] Univ Salamanca, Dept Biochem, Salamanca 37007, Spain
关键词
Vav family; Rho GEFs; DH domain; RhoA; Rac; Cdc42; cytoskeleton;
D O I
10.1038/sj.onc.1205000
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
Vav proteins are GDP/GTP exchange factors for Rho/Rac GTPases that are activated by tyrosine phosphorylation. These proteins activate Rac1, RhoG, and RhoA but not the highly related Cdc42 protein. At present, there is no available information to explain this substrate selectivity at the structural level. Here we show that the selection of Vav proteins substrates is achieved at two different levels. On one hand, Vav proteins utilize some residues of the beta2/beta3 region of Rho/Rac GTPases (D49 and E54) to assure the specific binding to its substrate. In addition, these exchange factors need a second structural signal located in the beta5 region of Rho/Rac proteins (residue K118) to promote proper GDP/GTP exchange. These results identify the amino acid residues that allow the discrimination of the Vav family substrates from Cdc42 and, in addition, demonstrate that the activation of specific Rho/Rac GTPases by these GEFs requires two concatenated events, binding and subsequent enzyme reaction, whose specificities are determined by two separate regions of Rho proteins.
引用
收藏
页码:8057 / 8065
页数:9
相关论文
共 17 条
[1]   Structural basis for relief of autoinhibition of the Dbl homology domain of proto-oncogene Vav by tyrosine phosphorylation [J].
Aghazadeh, B ;
Lowry, WE ;
Huang, XY ;
Rosen, MK .
CELL, 2000, 102 (05) :625-633
[2]   Regulatory and signaling properties of the Vav family [J].
Bustelo, XR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1461-1477
[3]   Phosphotyrosine-dependent activation of Rac-1 GDP/GTP exchange by the vav proto-oncogene product [J].
Crespo, P ;
Schuebel, KE ;
Ostrom, AA ;
Gutkind, JS ;
Bustelo, XR .
NATURE, 1997, 385 (6612) :169-172
[4]   Activation of Vav by Nef induces cytoskeletal rearrangements and downstream effector functions [J].
Fackler, OT ;
Luo, W ;
Geyer, M ;
Alberts, AS ;
Peterlin, BM .
MOLECULAR CELL, 1999, 3 (06) :729-739
[5]   DEFECTIVE T-CELL RECEPTOR SIGNALING AND POSITIVE SELECTION OF VAV-DEFICIENT CD4(+) CD8(+) THYMOCYTES [J].
FISCHER, KD ;
ZMUIDZINAS, A ;
GARDNER, S ;
BARBACID, M ;
BERNSTEIN, A ;
GUIDOS, C .
NATURE, 1995, 374 (6521) :474-477
[6]   Structure of the Rho family GTP-binding protein Cdc42 in complex with the multifunctional regulator RhoGDI [J].
Hoffman, GR ;
Nassar, N ;
Cerione, RA .
CELL, 2000, 100 (03) :345-356
[7]   Flipping the switch: The structural basis for signaling through the CRIB motif [J].
Hoffman, GR ;
Cerione, RA .
CELL, 2000, 102 (04) :403-406
[8]   A guanine nucleotide exchange factor-independent function of Vav1 in transcriptional activation [J].
Kuhne, MR ;
Ku, G ;
Weiss, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (03) :2185-2190
[9]   Residues of the Rho family GTPases Rho and Cdc42 that specify sensitivity to Dbl-like guanine nucleotide exchange factors [J].
Li, R ;
Zheng, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :4671-4679
[10]  
Movilla N, 1999, MOL CELL BIOL, V19, P7870