The p53 tumor suppressor targets a novel regulator of G protein signaling

被引:87
作者
Buckbinder, L
VelascoMiguel, S
Chen, Y
Xu, NZ
Talbott, R
Gelbert, L
Gao, JZ
Seizinger, BR
Gutkind, JS
Kley, N
机构
[1] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,DEPT MOL GENET,PRINCETON,NJ 08543
[2] NIDR,MOL SIGNALING UNIT,CELLULAR DEV & ONCOL LAB,NIH,BETHESDA,MD 20892
[3] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,DEPT BIOMOLEC DRUG DISCOVERY,PRINCETON,NJ 08543
关键词
D O I
10.1073/pnas.94.15.7868
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
Heterotrimeric G proteins transduce multiple growth-factor-receptor-initiated and intracellular signals that may lead to activation of the mitogen-activated or stress-activated protein kinases, Herein we report on the identification of a novel p53 target gene (A28-RGS14) that is induced in response to genotoxic stress and encodes a novel member of a family of regulators of G protein signaling (RGS) proteins with proposed GTPase-activating protein activity. Overexpression of A28-RGS14p protein inhibits both G(i)- and G(q)-coupled growth-factor-receptor-mediated activation of the mitogen-activated protein kinase signaling pathway in mammalian cells. Thus, through the induction of A28-RGS14, p53 may regulate cellular sensitivity to growth and/or survival factors acting through G protein-coupled receptor pathways.
引用
收藏
页码:7868 / 7872
页数:5
相关论文
共 24 条
[1]   ISOLATION OF A GENE REQUIRED FOR PROGRAMMED INITIATION OF DEVELOPMENT BY ASPERGILLUS-NIDULANS [J].
ADAMS, TH ;
HIDE, WA ;
YAGER, LN ;
LEE, BN .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (09) :3827-3833
[2]   GAIP and RGS4 are GTPase-activating proteins for the G(i) subfamily of G protein alpha subunits [J].
Berman, DM ;
Wilkie, TM ;
Gilman, AG .
CELL, 1996, 86 (03) :445-452
[3]   GENE-REGULATION BY TEMPERATURE-SENSITIVE P53 MUTANTS - IDENTIFICATION OF P53 RESPONSE GENES [J].
BUCKBINDER, L ;
TALBOTT, R ;
SEIZINGER, BR ;
KLEY, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10640-10644
[4]   INDUCTION OF THE GROWTH INHIBITOR IGF-BINDING PROTEIN-3 BY P53 [J].
BUCKBINDER, L ;
TALBOTT, R ;
VELASCOMIGUEL, S ;
TAKENAKA, I ;
FAHA, B ;
SEIZINGER, BR ;
KLEY, N .
NATURE, 1995, 377 (6550) :646-649
[5]   SIMILAR BIOCHEMICAL-CHANGES ASSOCIATED WITH MULTIDRUG RESISTANCE IN HUMAN-BREAST CANCER-CELLS AND CARCINOGEN-INDUCED RESISTANCE TO XENOBIOTICS IN RATS [J].
COWAN, KH ;
BATIST, G ;
TULPULE, A ;
SINHA, BK ;
MYERS, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9328-9332
[6]   RAS-DEPENDENT ACTIVATION OF MAP KINASE PATHWAY MEDIATED BY G-PROTEIN BETA-GAMMA-SUBUNITS [J].
CRESPO, P ;
XU, NZ ;
SIMONDS, WF ;
GUTKIND, JS .
NATURE, 1994, 369 (6479) :418-420
[7]   CONTROL OF ANGIOGENESIS IN FIBROBLASTS BY P53 REGULATION OF THROMBOSPONDIN-1 [J].
DAMERON, KM ;
VOLPERT, OV ;
TAINSKY, MA ;
BOUCK, N .
SCIENCE, 1994, 265 (5178) :1582-1584
[8]   GAIP, A PROTEIN THAT SPECIFICALLY INTERACTS WITH THE TRIMERIC G-PROTEIN G-ALPHA(I3), IS A MEMBER OF A PROTEIN FAMILY WITH A HIGHLY CONSERVED CORE DOMAIN [J].
DEVRIES, L ;
MOUSLI, M ;
WURMSER, A ;
FARQUHAR, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11916-11920
[9]  
DOHLMAN HG, 1995, MOL CELL BIOL, V15, P3635
[10]  
Dohlman HG, 1996, MOL CELL BIOL, V16, P5194