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

被引:1371
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 [J].
Abe, J ;
Kusuhara, M ;
Ulevitch, RJ ;
Berk, BC ;
Lee, JD .
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 [J].
ADLER, V ;
FRANKLIN, CC ;
KRAFT, AS .
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 [J].
ADLER, V ;
PINCUS, MR ;
BRANDTRAUF, PW ;
RONAI, Z .
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 [J].
Amano, M ;
Mukai, H ;
Ono, Y ;
Chihara, K ;
Matsui, T ;
Hamajima, Y ;
Okawa, K ;
Iwamatsu, A ;
Kaibuchi, K .
SCIENCE, 1996, 271 (5249) :648-650
[5]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
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 [J].
ARIAS, J ;
ALBERTS, AS ;
BRINDLE, P ;
CLARET, FX ;
SMEAL, T ;
KARIN, M ;
FERAMISCO, J ;
MONTMINY, M .
NATURE, 1994, 370 (6486) :226-229
[8]   MEMBRANE TARGETING OF THE NUCLEOTIDE EXCHANGE FACTOR SOS IS SUFFICIENT FOR ACTIVATING THE RAS SIGNALING PATHWAY [J].
ARONHEIM, A ;
ENGELBERG, D ;
LI, NX ;
ALALAWI, N ;
SCHLESSINGER, J ;
KARIN, M .
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 [J].
BANNISTER, AJ ;
KOUZARIDES, T .
EMBO JOURNAL, 1995, 14 (19) :4758-4762