Vav proteins, adaptors and cell signaling

被引:175
作者
Bustelo, XR
机构
[1] Univ Salamanca, Ctr Invest Canc, E-37007 Salamanca, Spain
[2] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, E-37007 Salamanca, Spain
关键词
Vav; exchange factors; Rho/Rac proteins; tyrosine kinase; adaptor proteins; Ca2+;
D O I
10.1038/sj.onc.1204780
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
The Vav family is a group of signal transduction molecules with oncogenic potential that play important roles in development and cell signaling. Members of this family are distributed in all animal metazoans but not in unicellular organisms. Recent genomic studies suggest that the function of Vav proteins co-evolved with tyrosine kinase pathways, probably to assure the optimal conversion of extracellular signals into biological responses coupled to the cytoskeleton and gene transcription. To date, the best-known function of Vav proteins is their role as GDP/GTP exchange factors for Rho/Rac molecules, a function strictly controlled by tyrosine phosphorylation. Recent publications indicate that this function is highly dependent on the interaction of adaptor proteins that aid in the proper phosphorylation of Vav proteins, their interaction with other signaling molecules, and in modulating the strength of their signal outputs. In addition to the function of Vav proteins as exchange factors, there is increasing evidence suggesting that Vav proteins can mediate other cellular functions independently of their exchange activities, probably by working themselves as adaptor molecules. In this review, we will give a summary of the recent advances in this field, placing special emphasis on the non-catalytic roles of Vav and its interaction with other adaptor molecules.
引用
收藏
页码:6372 / 6381
页数:10
相关论文
共 55 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]   The Src homology 2 domain of Vav is required for its compartmentation to the plasma membrane and activation of C-jun NH2-terminal kinase 1 [J].
Arudchandran, R ;
Brown, MJ ;
Peirce, MJ ;
Song, JS ;
Zhang, JA ;
Siraganian, RP ;
Blank, U ;
Rivera, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (01) :47-59
[3]   Specific subdomains of Vav differentially affect T cell and NK cell activation [J].
Billadeau, DD ;
Mackie, SM ;
Schoon, RA ;
Leibson, PJ .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :3971-3981
[4]   SH3-mediated Hck tyrosine kinase activation and fibroblast transformation by the Nef protein of HIV-1 [J].
Briggs, SD ;
Sharkey, M ;
Stevenson, M ;
Smithgall, TE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (29) :17899-17902
[5]   Regulatory and signaling properties of the Vav family [J].
Bustelo, XR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1461-1477
[6]   The Rho-family GTP exchange factor Vav is a critical transducer of T cell receptor signals to the calcium, ERK, and NF-κB pathways [J].
Costello, PS ;
Walters, AE ;
Mee, PJ ;
Turner, M ;
Reynolds, LF ;
Prisco, A ;
Sarner, N ;
Zamoyska, R ;
Tybulewicz, VLJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :3035-3040
[7]   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
[8]   Vav-2 controls NFAT-dependent transcription in B- but not T-lymphocytes [J].
Doody, GM ;
Billadeau, DD ;
Clayton, E ;
Hutchings, A ;
Berland, R ;
McAdam, S ;
Leibson, PJ ;
Turner, M .
EMBO JOURNAL, 2000, 19 (22) :6173-6184
[9]  
DOODY GM, 2001, NAT IMMUNOL, V6, P482
[10]   RasGRP essential for mouse thymocyte differentiation and TCR signaling [J].
Dower, NA ;
Stang, SL ;
Bottorff, DA ;
Ebinu, JO ;
Dickie, P ;
Ostergaard, HL ;
Stone, JC .
NATURE IMMUNOLOGY, 2000, 1 (04) :317-321