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
    ADAMS, TH
    HIDE, WA
    YAGER, LN
    LEE, BN
    [J]. 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
    Berman, DM
    Wilkie, TM
    Gilman, AG
    [J]. CELL, 1996, 86 (03) : 445 - 452
  • [3] GENE-REGULATION BY TEMPERATURE-SENSITIVE P53 MUTANTS - IDENTIFICATION OF P53 RESPONSE GENES
    BUCKBINDER, L
    TALBOTT, R
    SEIZINGER, BR
    KLEY, N
    [J]. 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
    BUCKBINDER, L
    TALBOTT, R
    VELASCOMIGUEL, S
    TAKENAKA, I
    FAHA, B
    SEIZINGER, BR
    KLEY, N
    [J]. 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
    COWAN, KH
    BATIST, G
    TULPULE, A
    SINHA, BK
    MYERS, CE
    [J]. 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
    CRESPO, P
    XU, NZ
    SIMONDS, WF
    GUTKIND, JS
    [J]. NATURE, 1994, 369 (6479) : 418 - 420
  • [7] CONTROL OF ANGIOGENESIS IN FIBROBLASTS BY P53 REGULATION OF THROMBOSPONDIN-1
    DAMERON, KM
    VOLPERT, OV
    TAINSKY, MA
    BOUCK, N
    [J]. 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
    DEVRIES, L
    MOUSLI, M
    WURMSER, A
    FARQUHAR, MG
    [J]. 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