Functional and physical interactions of Syk family kinases with the Vav proto-oncogene product

被引:244
作者
Deckert, M
TartareDeckert, S
Couture, C
Mustelin, T
Altman, A
机构
[1] LA JOLLA INST ALLERGY & IMMUNOL, DIV CELL BIOL, SAN DIEGO, CA 92121 USA
[2] FAC MED NICE, INSERM, U145, F-06107 NICE 2, FRANCE
关键词
D O I
10.1016/S1074-7613(00)80273-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Syk family kinases are essential for lymphocyte development and activation. Therefore the identification of their direct effecters is of critical importance. Here, we report that Syk interacts in the yeast two-hybrid system with Vav, a proto-oncogene product exclusively expressed in hematopoietic cells. This interaction was direct, required the catalytic activity of Syk, the SH2 domain of Vav, and tyrosine residues in the linker domain of Syk. Vav also associated with Syk and Zap in antigen receptor-stimulated B or T cells, respectively. Functionally, Vav was phosphorylated by Syk family kinases both in vivo and in vitro. Furthermore, Syk and Vav cooperated to activate NF-AT synergistically, These results indicate that the interaction between Syk family kinases and Vav plays an important role in coupling immune recognition receptors to signaling pathways involved in lymphokine production.
引用
收藏
页码:591 / 604
页数:14
相关论文
共 52 条
[1]   DEFECTIVE T-CELL RECEPTOR SIGNALING AND CD8(+) THYMIC SELECTION IN HUMANS LACKING ZAP-70 KINASE [J].
ARPAIA, E ;
SHAHAR, M ;
DADI, H ;
COHEN, A ;
ROIFMAN, CM .
CELL, 1994, 76 (05) :947-958
[2]  
Ausubel F.M., 1992, CURRENT PROTOCOLS MO
[3]  
BARTEL PL, 1995, METHOD ENZYMOL, V254, P241
[4]   Vav: Function and regulation in hematopoietic cell signaling [J].
BonnefoyBerard, N ;
Munshi, A ;
Yron, I ;
Wu, SK ;
Collins, TL ;
Deckert, M ;
ShalomBarak, T ;
Giampa, L ;
Herbert, E ;
Hernandez, J ;
Meller, N ;
Couture, C ;
Altman, A .
STEM CELLS, 1996, 14 (03) :250-268
[5]   SITE-SPECIFICITY OF P72(SYK) PROTEIN-TYROSINE KINASE - EFFICIENT PHOSPHORYLATION OF MOTIFS RECOGNIZED BY SRC HOMOLOGY-2 DOMAINS OF THE SRC FAMILY [J].
BRUNATI, AM ;
DONELLADEANA, A ;
RUZZENE, M ;
MARIN, O ;
PINNA, LA .
FEBS LETTERS, 1995, 367 (02) :149-152
[6]   PRODUCT OF VAV PROTOONCOGENE DEFINES A NEW CLASS OF TYROSINE PROTEIN-KINASE SUBSTRATES [J].
BUSTELO, XR ;
LEDBETTER, JA ;
BARBACID, M .
NATURE, 1992, 356 (6364) :68-71
[7]   NEW NOMENCLATURE FOR THE RETH MOTIF (OR ARH1/TAM/ARAM/YXXL) [J].
CAMBIER, JC ;
DAERON, M ;
FRIDMAN, W ;
GERGELY, J ;
KINET, JP ;
KLAUSNER, R ;
LYNCH, R ;
MALISSEN, B ;
PECHT, I ;
REINHERZ, E ;
RAVETCH, J ;
RETH, M ;
SAMELSON, L ;
SANDOR, M ;
SCHREIBER, A ;
SEED, B ;
TERHORST, C ;
VANDEWINKEL, J ;
WEISS, A .
IMMUNOLOGY TODAY, 1995, 16 (02) :110-110
[8]   ZAP-70 DEFICIENCY IN AN AUTOSOMAL RECESSIVE FORM OF SEVERE COMBINED IMMUNODEFICIENCY [J].
CHAN, AC ;
KADLECEK, TA ;
ELDER, ME ;
FILIPOVICH, AH ;
KUO, WL ;
IWASHIMA, M ;
PARSLOW, TG ;
WEISS, A .
SCIENCE, 1994, 264 (5165) :1599-1601
[9]   SYK TYROSINE KINASE REQUIRED FOR MOUSE VIABILITY AND B-CELL DEVELOPMENT [J].
CHENG, AM ;
ROWLEY, B ;
PAO, W ;
HAYDAY, A ;
BOLEN, JB ;
PAWSON, T .
NATURE, 1995, 378 (6554) :303-306
[10]   ACTIVATION OF P56(LCK) BY P72(SYK) THROUGH PHYSICAL ASSOCIATION AND N-TERMINAL TYROSINE PHOSPHORYLATION [J].
COUTURE, C ;
BAIER, G ;
OETKEN, C ;
WILLIAMS, S ;
TELFORD, D ;
MARIECARDINE, A ;
BAIERBITTERLICH, G ;
FISCHER, S ;
BURN, P ;
ALTMAN, A ;
MUSTELIN, T .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) :5249-5258