POLYOMA MIDDLE TUMOR-ANTIGEN INTERACTS WITH SHC PROTEIN VIA THE NPTY (ASN-PRO-THR-TYR) MOTIF IN MIDDLE TUMOR-ANTIGEN

被引:160
作者
CAMPBELL, KS
OGRIS, E
BURKE, B
SU, W
AUGER, KR
DRUKER, BJ
SCHAFFHAUSEN, BS
ROBERTS, TM
PALLAS, DC
机构
[1] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, DIV CELL & MOLEC BIOL, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02115 USA
[3] OREGON HLTH SCI UNIV, DIV HEMATOL & MED ONCOL, PORTLAND, OR 97201 USA
[4] TUFTS UNIV, SCH MED, DEPT BIOCHEM, BOSTON, MA 02111 USA
关键词
D O I
10.1073/pnas.91.14.6344
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polyomavirus middle tumor antigen (MT) transforms a large number of cell types by binding to and modulating the activities of cellular proteins. Previous genetic analysis defined in MT an independent motif, NPTY (Asn-Pro-Thr-Tyr), required for transformation. This report demonstrates that NPTY is required for interaction between MT and SHC protein, a Src homology 2 (SH2)-containing protooncogene product implicated in activating Ras via association with GRB2 protein. SHC is phosphorylated on tyrosine and associates with GRB2 in MT-transformed cells. These effects require an intact NPTY motif in MT. SHC immunoprecipitates from MT-transformed cells possess kinase activity that phosphorylates not only SHC and MT but also the 85-kDa subunit of phosphatidylinositol 3-kinase. This result suggests that a complex exists that contains, at a minimum, MT, Src family tyrosine kinases, phosphatidylinositol 3-kinase, and SHC.
引用
收藏
页码:6344 / 6348
页数:5
相关论文
共 54 条
[1]  
AUGER KR, 1992, J BIOL CHEM, V267, P5408
[2]   BINDING OF THE SRC SH2 DOMAIN TO PHOSPHOPEPTIDES IS DETERMINED BY RESIDUES IN BOTH THE SH2 DOMAIN AND THE PHOSPHOPEPTIDES [J].
BIBBINS, KB ;
BOEUF, H ;
VARMUS, HE .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) :7278-7287
[3]   ENHANCEMENT OF CELLULAR SRC GENE-PRODUCT ASSOCIATED TYROSYL KINASE-ACTIVITY FOLLOWING POLYOMA-VIRUS INFECTION AND TRANSFORMATION [J].
BOLEN, JB ;
THIELE, CJ ;
ISRAEL, MA ;
YONEMOTO, W ;
LIPSICH, LA ;
BRUGGE, JS .
CELL, 1984, 38 (03) :767-777
[4]   ONCOGENES AND SIGNAL TRANSDUCTION [J].
CANTLEY, LC ;
AUGER, KR ;
CARPENTER, C ;
DUCKWORTH, B ;
GRAZIANI, A ;
KAPELLER, R ;
SOLTOFF, S .
CELL, 1991, 64 (02) :281-302
[5]   TRANSFORMATION BY POLYOMA-VIRUS IS DRASTICALLY REDUCED BY SUBSTITUTION OF PHENYLALANINE FOR TYROSINE AT RESIDUE-315 OF MIDDLE-SIZED TUMOR-ANTIGEN [J].
CARMICHAEL, G ;
SCHAFFHAUSEN, BS ;
MANDEL, G ;
LIANG, TJ ;
BENJAMIN, TL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (03) :679-683
[6]  
CARMICHAEL GG, 1980, J BIOL CHEM, V255, P230
[7]   STRUCTURAL AND FUNCTIONAL MODIFICATION OF PP60C-SRC ASSOCIATED WITH POLYOMA MIDDLE TUMOR-ANTIGEN FROM INFECTED OR TRANSFORMED-CELLS [J].
CARTWRIGHT, CA ;
HUTCHINSON, MA ;
ECKHART, W .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (10) :2647-2652
[8]  
CHEN WJ, 1990, J BIOL CHEM, V265, P3116
[9]   RECOMBINANT RETROVIRUSES THAT TRANSDUCE INDIVIDUAL POLYOMA TUMOR-ANTIGENS - EFFECTS ON GROWTH AND DIFFERENTIATION [J].
CHERINGTON, V ;
MORGAN, B ;
SPIEGELMAN, BM ;
ROBERTS, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) :4307-4311
[10]   TYROSINE PHOSPHORYLATION IS A SIGNAL FOR THE TRAFFICKING OF PP85, AN 85-KDA PHOSPHORYLATED POLYPEPTIDE ASSOCIATED WITH PHOSPHATIDYLINOSITOL KINASE-ACTIVITY [J].
COHEN, B ;
YOAKIM, M ;
PIWNICAWORMS, H ;
ROBERTS, TM ;
SCHAFFHAUSEN, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4458-4462