Transcription factor AP-1, and the role of Fra-2

被引:92
作者
Foletta, VC
机构
[1] Div. of Immunology and Cell Biology, John Curtin Sch. of Medical Research, Australian National University, Canberra, ACT
[2] Div. of Immunology and Cell Biology, John Curtin Sch. of Medical Research, Australian National University, Canberra
关键词
fos genes; fos-related antigens; gene expression regulation; immediate-early genes; jun genes; transcription factor AP-1; transcription factors; SERUM RESPONSE ELEMENT; C-FOS EXPRESSION; TISSUE-SPECIFIC EXPRESSION; DNA-BINDING ACTIVITY; RNA POLYMERASE-II; PROTEIN-KINASE-C; SIGNAL-TRANSDUCTION PATHWAYS; IMMEDIATE-EARLY GENE; TRANSGENIC MICE; GROWTH-FACTORS;
D O I
10.1038/icb.1996.17
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcription factors function to regulate gene transcription. They may be constitutively expressed or may only be activated during specific situations. Activator protein-1 (AP-I) is an inducible transcription factor, and is comprised of multiple protein complexes that include the gene products of the fos and jun gene families. Numerous cellular and viral genes contain AP-1 binding sites within their promoters and, accordingly, AP-I has been shown to play a role in the regulation of both basal and inducible transcription of these genes. fos-related antigen-2 (fra-2) has been found to have both similar and unique properties to that of other fos gene members in terms of its regulation and expression. The analysis and determination of the function of Fra-2 will provide further information on the role of AP-1.
引用
收藏
页码:121 / 133
页数:13
相关论文
共 163 条
  • [51] C-JUN DIMERIZES WITH ITSELF AND WITH C-FOS, FORMING COMPLEXES OF DIFFERENT DNA-BINDING AFFINITIES
    HALAZONETIS, TD
    GEORGOPOULOS, K
    GREENBERG, ME
    LEDER, P
    [J]. CELL, 1988, 55 (05) : 917 - 924
  • [52] OCCUPATION OF THE C-FOS SERUM RESPONSE ELEMENT INVIVO BY A MULTI-PROTEIN COMPLEX IS UNALTERED BY GROWTH-FACTOR INDUCTION
    HERRERA, RE
    SHAW, PE
    NORDHEIM, A
    [J]. NATURE, 1989, 340 (6228) : 68 - 70
  • [53] HERSCHMAN HR, 1991, ANNU REV BIOCHEM, V60, P281, DOI 10.1146/annurev.bi.60.070191.001433
  • [54] IDENTIFICATION OF AN ONCOPROTEIN-RESPONSIVE AND UV-RESPONSIVE PROTEIN-KINASE THAT BINDS AND POTENTIATES THE C-JUN ACTIVATION DOMAIN
    HIBI, M
    LIN, AN
    SMEAL, T
    MINDEN, A
    KARIN, M
    [J]. GENES & DEVELOPMENT, 1993, 7 (11) : 2135 - 2148
  • [55] C-JUN IS ESSENTIAL FOR NORMAL MOUSE DEVELOPMENT AND HEPATOGENESIS
    HILBERG, F
    AGUZZI, A
    HOWELLS, N
    WAGNER, EF
    [J]. NATURE, 1993, 365 (6442) : 179 - 181
  • [56] TRANSIENT ACTIVATION OF RAF-1, MEK, AND ERK2 COINCIDES KINETICALLY WITH TERNARY COMPLEX FACTOR PHOSPHORYLATION AND IMMEDIATE-EARLY GENE PROMOTER ACTIVITY IN-VIVO
    HIPSKIND, RA
    BACCARINI, M
    NORDHEIM, A
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) : 6219 - 6231
  • [57] ETS-RELATED PROTEIN ELK-1 IS HOMOLOGOUS TO THE C-FOS REGULATORY FACTOR P62TCF
    HIPSKIND, RA
    RAO, VN
    MUELLER, CGF
    REDDY, ESP
    NORDHEIM, A
    [J]. NATURE, 1991, 354 (6354) : 531 - 534
  • [58] CHARACTERIZATION OF JUND - A NEW MEMBER OF THE JUN PROTO-ONCOGENE FAMILY
    HIRAI, SI
    RYSECK, RP
    MECHTA, F
    BRAVO, R
    YANIV, M
    [J]. EMBO JOURNAL, 1989, 8 (05) : 1433 - 1439
  • [59] MOLECULAR-CLONING AND FUNCTIONAL-ANALYSIS OF DROSOPHILA TAF110 REVEAL PROPERTIES EXPECTED OF COACTIVATORS
    HOEY, T
    WEINZIERL, ROJ
    GILL, G
    CHEN, JL
    DYNLACHT, BD
    TJIAN, R
    [J]. CELL, 1993, 72 (02) : 247 - 260
  • [60] INDUCIBLE PRODUCTION OF C-FOS ANTISENSE RNA INHIBITS 3T3 CELL-PROLIFERATION
    HOLT, JT
    GOPAL, TV
    MOULTON, AD
    NIENHUIS, AW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (13) : 4794 - 4798