Phosphatidylinositol 3' kinase: One of the effectors of Ras

被引:66
作者
RodriguezViciana, P
Marte, BM
Warne, PH
Downward, J
机构
[1] Imperial Cancer Research Fund, London WC2A 3PX
关键词
D O I
10.1098/rstb.1996.0020
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ras proteins are proto-oncogene products that are critical components of signalling pathways leading from cell surface receptors to control of cellular proliferation, morphology and differentiation. The ability of Ras to activate the MAP kinase pathway through interaction with the serine/threonine kinase Raf is now well established. However, recent work has shown that Ras can also interact directly with the catalytic subunit of phosphatidylinositol 3' kinase and is involved in control of the lipid kinase in intact cells. A model is presented in which both tyrosine phosphoprotein interaction with the regulatory p85 subunit and Ras. GTP interaction with the catalytic p110 subunit is required to achieve optimal activation of phosphatidylinositol 3' kinase in response to extracellular stimuli. The ability of Ras to regulate phosphatidylinositol 3' kinase may be important both in Ras control of cellular morphology through the actin cytoskeleton and also in Ras control of DNA synthesis.
引用
收藏
页码:225 / 231
页数:7
相关论文
共 46 条
[1]   CHARACTERIZATION OF A GUANINE-NUCLEOTIDE DISSOCIATION STIMULATOR FOR A RAS-RELATED GTPASE [J].
ALBRIGHT, CF ;
GIDDINGS, BW ;
LIU, J ;
VITO, M ;
WEINBERG, RA .
EMBO JOURNAL, 1993, 12 (01) :339-347
[2]   INDUCTION OF MEMBRANE RUFFLING AND FLUID-PHASE PINOCYTOSIS IN QUIESCENT FIBROBLASTS BY RAS PROTEINS [J].
BARSAGI, D ;
FERAMISCO, JR .
SCIENCE, 1986, 233 (4768) :1061-1068
[3]   EPIDERMAL GROWTH-FACTOR INDUCES PHOSPHORYLATION OF EXTRACELLULAR SIGNAL-REGULATED KINASE-2 VIA MULTIPLE PATHWAYS [J].
BURGERING, BMT ;
DEVRIESSMITS, AMM ;
MEDEMA, RH ;
VANWEEREN, PC ;
TERTOOLEN, LGJ ;
BOS, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) :7248-7256
[4]   POLYOMA MIDDLE TUMOR-ANTIGEN INTERACTS WITH SHC PROTEIN VIA THE NPTY (ASN-PRO-THR-TYR) MOTIF IN MIDDLE TUMOR-ANTIGEN [J].
CAMPBELL, KS ;
OGRIS, E ;
BURKE, B ;
SU, W ;
AUGER, KR ;
DRUKER, BJ ;
SCHAFFHAUSEN, BS ;
ROBERTS, TM ;
PALLAS, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6344-6348
[5]  
CARTER AN, 1992, J BIOL CHEM, V267, P14563
[6]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[7]  
DICKMANN D, 1991, NATURE, V351, P400
[8]   TRANSFORMATION BY POLYOMA-VIRUS MIDDLE T-ANTIGEN INVOLVES THE BINDING AND TYROSINE PHOSPHORYLATION OF SHC [J].
DILWORTH, SM ;
BREWSTER, CEP ;
JONES, MD ;
LANFRANCONE, L ;
PELICCI, G ;
PELICCI, PG .
NATURE, 1994, 367 (6458) :87-90
[9]   IDENTIFICATION OF THE SH3 DOMAIN OF GAP AS AN ESSENTIAL SEQUENCE FOR RAS-GAP MEDIATED SIGNALING [J].
DUCHESNE, M ;
SCHWEIGHOFFER, F ;
PARKER, F ;
CLERC, F ;
FROBERT, Y ;
THANG, MN ;
TOCQUE, B .
SCIENCE, 1993, 259 (5094) :525-528
[10]   P21RAS ACTIVATION VIA HEMOPOIETIN RECEPTORS AND C-KIT REQUIRES TYROSINE KINASE-ACTIVITY BUT NOT TYROSINE PHOSPHORYLATION OF P21RAS GTPASE-ACTIVATING PROTEIN [J].
DURONIO, V ;
WELHAM, MJ ;
ABRAHAM, S ;
DRYDEN, P ;
SCHRADER, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) :1587-1591