Transcription factor AP-1 regulation by mitogen-activated protein kinase signal transduction pathways

被引:1361
作者
Whitmarsh, AJ
Davis, RJ
机构
[1] UNIV MASSACHUSETTS,SCH MED,HOWARD HUGHES MED INST,WORCESTER,MA 01605
[2] UNIV MASSACHUSETTS,SCH MED,DEPT BIOCHEM & MOL BIOL,PROGRAM MOL MED,WORCESTER,MA 01605
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1996年 / 74卷 / 10期
关键词
signal transduction; mitogen-activated protein kinase; AP-1; c-Fos; c-Jun;
D O I
10.1007/s001090050063
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mitogen-activated protein (MAP) kinases are proline-directed serine/threonine kinases that are activated by dual, phosphorylation on threonine and tyrosine residues in response to a wide array of extracellular stimuli. Three distinct groups of MAP kinases have been identified in mammalian cells [extracellular-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38]. These MAP kinases are mediators of signal transduction from the cell surface to the nucleus. One nuclear target of these MAP kinase signaling pathways is the transcription factor AP-1. MAP kinases regulate AP-1 transcriptional activity by multiple mechanisms. Here we review recent progress towards understanding AP-1 regulation by the ERK, JNK, and p38 MAP kinase signal transduction pathways.
引用
收藏
页码:589 / 607
页数:19
相关论文
共 234 条
  • [1] Big mitogen-activated protein kinase 1 (BMK1) is a redox-sensitive kinase
    Abe, J
    Kusuhara, M
    Ulevitch, RJ
    Berk, BC
    Lee, JD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) : 16586 - 16590
  • [2] PHORBOL ESTERS STIMULATE THE PHOSPHORYLATION OF C-JUN BUT NOT V-JUN - REGULATION BY THE N-TERMINAL DELTA DOMAIN
    ADLER, V
    FRANKLIN, CC
    KRAFT, AS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) : 5341 - 5345
  • [3] COMPLEXES OF P21(RAS) WITH JUN N-TERMINAL KINASE AND JUN PROTEINS
    ADLER, V
    PINCUS, MR
    BRANDTRAUF, PW
    RONAI, Z
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) : 10585 - 10589
  • [4] Identification of a putative target for Rho as the serine-threonine kinase protein kinase N
    Amano, M
    Mukai, H
    Ono, Y
    Chihara, K
    Matsui, T
    Hamajima, Y
    Okawa, K
    Iwamatsu, A
    Kaibuchi, K
    [J]. SCIENCE, 1996, 271 (5249) : 648 - 650
  • [5] THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION
    ANGEL, P
    KARIN, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) : 129 - 157
  • [6] ANGEL P, 1995, INDUCIBLE GENE EXPRE, V1, P63
  • [7] ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR
    ARIAS, J
    ALBERTS, AS
    BRINDLE, P
    CLARET, FX
    SMEAL, T
    KARIN, M
    FERAMISCO, J
    MONTMINY, M
    [J]. NATURE, 1994, 370 (6486) : 226 - 229
  • [8] MEMBRANE TARGETING OF THE NUCLEOTIDE EXCHANGE FACTOR SOS IS SUFFICIENT FOR ACTIVATING THE RAS SIGNALING PATHWAY
    ARONHEIM, A
    ENGELBERG, D
    LI, NX
    ALALAWI, N
    SCHLESSINGER, J
    KARIN, M
    [J]. CELL, 1994, 78 (06) : 949 - 961
  • [9] BAGRODIA S, 1995, J BIOL CHEM, V270, P27995
  • [10] CBP-INDUCED STIMULATION OF C-FOS ACTIVITY IS ABROGATED BY E1A
    BANNISTER, AJ
    KOUZARIDES, T
    [J]. EMBO JOURNAL, 1995, 14 (19) : 4758 - 4762