Functional interaction of RasGAP-binding proteins Dok-1 and Dok-2 with the Tec protein tyrosine kinase

被引:33
作者
Gérard, A
Favre, C
Garçon, F
Némorin, JG
Duplay, P
Pastor, S
Collette, Y
Olive, D
Nunès, JA
机构
[1] Univ Mediterranee, Inst Canc & Immunol Marseille, INSERM, U119, F-13009 Marseille, France
[2] Univ Quebec, Inst Armand Frappier, Inst Natl Rech Sci, Laval, PQ, Canada
基金
加拿大健康研究院;
关键词
Dok adaptor proteins; Tec tyrosine kinase; signal transduction; tumor suppressors; T cells;
D O I
10.1038/sj.onc.1207283
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 Dok adaptor family of proteins binding to RasGAP, consisting of Dok-1 and Dok-2, are critical regulators in cell proliferation. These molecules are partners and/or substrates of different protein tyrosine kinases considered as oncoproteins. Here, we show that Dok-1 and Dok-2 are the major tyrosine-phosphorylated proteins associated to Tec, a protein tyrosine kinase expressed in T cells. Furthermore, we evaluate the effect of Dok-1 or Dok-2 on Tec-mediated signalling pathways in T cells. Here, we provide evidence that Dok-1 and Dok-2 proteins are involved in a negative feedback regulation of Tec via a downregulation of its tyrosine phosphorylation and downstream signalling pathways including the Ras pathway. Either Dok-1 or Dok-2 therefore represents a mean of potent retrograde control for protein tyrosine kinase signalling, and then possibly of tumor development.
引用
收藏
页码:1594 / 1598
页数:5
相关论文
共 23 条
[1]   Interactions of p62dok with p210bcr-abl and Bcr-Abl-associated proteins [J].
Bhat, A ;
Johnson, KJ ;
Oda, T ;
Corbin, AS ;
Druker, BJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :32360-32368
[2]   p62(dok): A constitutively tyrosine-phosphorylated, GAP-associated protein in chronic myelogenous leukemia progenitor cells [J].
Carpino, N ;
Wisniewski, D ;
Strife, A ;
Marshak, D ;
Kobayashi, R ;
Stillman, B ;
Clarkson, B .
CELL, 1997, 88 (02) :197-204
[3]  
CLARKSON B, 1993, LEUKEMIA, V7, P1683
[4]   Molecular cloning and characterization of p56dok-2 defines a new family of RasGAP-binding proteins [J].
Di Cristofano, A ;
Carpino, N ;
Dunant, N ;
Friedland, G ;
Kobayashi, R ;
Strife, A ;
Wisniewski, D ;
Clarkson, B ;
Pandolfi, PP ;
Resh, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :4827-4830
[5]   p62dok, a negative regulator of Ras and mitogen-activated protein kinase (MAPK) activity, opposes leukemogenesis by p210bcr-abl [J].
Di Cristofano, A ;
Niki, M ;
Zhao, MM ;
Karnell, FG ;
Clarkson, B ;
Pear, WS ;
Van Aelst, L ;
Pandolfi, PP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (03) :275-284
[6]   Dok-related protein negatively regulates T cell development via its RasGTPase-activating protein and Nck docking sites [J].
Gugasyan, R ;
Quilici, C ;
I, STT ;
Grail, D ;
Verhagen, AM ;
Roberts, A ;
Kitamura, T ;
Dunn, AR ;
Lock, P .
JOURNAL OF CELL BIOLOGY, 2002, 158 (01) :115-125
[7]   Dockers at the crossroads [J].
Guy, GR ;
Yusoff, P ;
Bangarusamy, D ;
Fong, CW ;
Wong, ESM .
CELLULAR SIGNALLING, 2002, 14 (01) :11-20
[8]   P21(RAS) COUPLES THE T-CELL ANTIGEN RECEPTOR TO EXTRACELLULAR SIGNAL-REGULATED KINASE-2 IN T-LYMPHOCYTES [J].
IZQUIERDO, M ;
LEEVERS, SJ ;
MARSHALL, CJ ;
CANTRELL, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) :1199-1208
[9]   Recruitment of Dok-R to the EGF receptor through its PTB domain is required for attenuation of Erk MAP kinase activation [J].
Jones, N ;
Dumont, DJ .
CURRENT BIOLOGY, 1999, 9 (18) :1057-1060
[10]   Phosphatidylinositol 3-kinase and Src family kinases are required for phosphorylation and membrane recruitment of Dok-1 in c-Kit signaling [J].
Liang, XQ ;
Wisniewski, D ;
Strife, A ;
Shivakrupa ;
Clarkson, B ;
Resh, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) :13732-13738