THE GAP-RELATED DOMAIN OF THE NEUROFIBROMATOSIS TYPE-1 GENE-PRODUCT INTERACTS WITH RAS P21

被引:861
作者
MARTIN, GA
VISKOCHIL, D
BOLLAG, G
MCCABE, PC
CROSIER, WJ
HAUBRUCK, H
CONROY, L
CLARK, R
OCONNELL, P
CAWTHON, RM
INNIS, MA
MCCORMICK, F
机构
[1] UNIV UTAH,SCH MED,DEPT PEDIAT,SALT LAKE CITY,UT 84132
[2] UNIV UTAH,SCH MED,DEPT HUMAN GENET,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
关键词
D O I
10.1016/0092-8674(90)90150-D
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 neurofibromatosis type 1 (NF1) protein contains a region of significant sequence similarity to ras p21 GTPase-activating protein (GAP) and the yeast IRA1 gene product. A fragment of NF1 cDNA encoding the GAP-related domain (NF1 GRD) was expressed, immunoaffinity purified, and assayed for effects on N-ras p21 GTPase activity. The GTPase of wild-type ras p21 was stimulated by NF1 GRD, but oncogenic mutants of ras p21 (Asp-12 and Val-12) were unaffected, and the GTPase of an effector mutant (Ala-38) was only weakly stimulated. NF1 GRD also down-regulated RAS function in S. cerevisiae. The affinity of NF1 GRD for ras p21 was estimated to be 250 nM: this is more than 20-fold higher than the affinity of GAP for ras p21. However, its specific activity was about 30 times lower. These kinetic measurements suggest that NF1 may be a significant regulator of ras p21 activity, particularly at low ras p21 concentrations. © 1990.
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页码:843 / 849
页数:7
相关论文
共 42 条
[1]   GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN (GAP) INTERACTS WITH THE P21-RAS EFFECTOR BINDING DOMAIN [J].
ADARI, H ;
LOWY, DR ;
WILLUMSEN, BM ;
DER, CJ ;
MCCORMICK, F .
SCIENCE, 1988, 240 (4851) :518-520
[2]   GENETIC-ANALYSIS OF MAMMALIAN GAP EXPRESSED IN YEAST [J].
BALLESTER, R ;
MICHAELI, T ;
FERGUSON, K ;
XU, HP ;
MCCORMICK, F ;
WIGLER, M .
CELL, 1989, 59 (04) :681-686
[3]   MICROINJECTION OF THE RAS ONCOGENE PROTEIN INTO PC12 CELLS INDUCES MORPHOLOGICAL-DIFFERENTIATION [J].
BARSAGI, D ;
FERAMISCO, JR .
CELL, 1985, 42 (03) :841-848
[4]  
BORASIO GD, 1989, NEURON, V2, P1087
[5]  
BOS JL, 1989, CANCER RES, V49, P4682
[6]   DIFFERENTIAL ACTIVATION OF YEAST ADENYLATE-CYCLASE BY WILD-TYPE AND MUTANT RAS PROTEINS [J].
BROEK, D ;
SAMIY, N ;
FASANO, O ;
FUJIYAMA, A ;
TAMANOI, F ;
NORTHUP, J ;
WIGLER, M .
CELL, 1985, 41 (03) :763-769
[7]   SEQUENCE HOMOLOGY SHARED BY NEUROFIBROMATOSIS TYPE-1 GENE AND IRA-1 AND IRA-2 NEGATIVE REGULATORS OF THE RAS CYCLIC-AMP PATHWAY [J].
BUCHBERG, AM ;
CLEVELAND, LS ;
JENKINS, NA ;
COPELAND, NG .
NATURE, 1990, 347 (6290) :291-294
[8]   A MAJOR SEGMENT OF THE NEUROFIBROMATOSIS TYPE-1 GENE - CDNA SEQUENCE, GENOMIC STRUCTURE, AND POINT MUTATIONS [J].
CAWTHON, RM ;
WEISS, R ;
XU, GF ;
VISKOCHIL, D ;
CULVER, M ;
STEVENS, J ;
ROBERTSON, M ;
DUNN, D ;
GESTELAND, R ;
OCONNELL, P ;
WHITE, R .
CELL, 1990, 62 (01) :193-201
[9]   PHOSPHORYLATION OF GAP AND GAP-ASSOCIATED PROTEINS BY TRANSFORMING AND MITOGENIC TYROSINE KINASES [J].
ELLIS, C ;
MORAN, M ;
MCCORMICK, F ;
PAWSON, T .
NATURE, 1990, 343 (6256) :377-381
[10]   Inhibition of GTPase activating protein stimulation of Ras-p21 GTPase by the Krev-1 gene product [J].
Frech, M ;
John, J ;
Pizon, V ;
Chardin, P ;
Tavitian, A ;
Clark, R ;
Mccormick, F ;
Wittinghofer, A .
SCIENCE, 1990, 249 (4965) :169-171