YEAST GCN4 AS A PROBE FOR ONCOGENESIS BY AP-1 TRANSCRIPTION FACTORS - TRANSCRIPTIONAL ACTIVATION THROUGH AP-1 SITES IS NOT SUFFICIENT FOR CELLULAR-TRANSFORMATION

被引:61
作者
OLIVIERO, S
ROBINSON, GS
STRUHL, K
SPIEGELMAN, BM
机构
[1] UNIV PADUA,DIPARTIMENTO BIOL,I-35121 PADUA,ITALY
[2] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV NAVAL ARCHITECTURE,BOSTON,MA 02115
关键词
YEAST GCN4; JUN; FOS; AP-1 TRANSCRIPTION FACTORS; ONCOGENESIS; CELLULAR TRANSFORMATION;
D O I
10.1101/gad.6.9.1799
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Jun and Fos oncoproteins belong to the AP-1 family of transcriptional activators and are believed to induce cellular transformation by inappropriately activating genes involved in cell replication. To determine whether transcriptional activation through AP-1 sites is sufficient for transforming activity, we examined the properties of an autonomous and heterologous AP-1 protein, yeast GCN4, in rat embryo fibroblasts. GCN4 induces transcriptional activation through AP-1 sites but, unlike Jun and Fos, fails to induce cellular transformation, in cooperation with Ha-ras. Jun-GCN4 and Fos-GCN4 homodimers independently induce cellular transformation indicating that the amino-terminal regions of Jun and Fos each contain regulatory functions that are required for oncogenesis but are distinct from generic transcriptional activation domains. In addition, these observations have implications for the nature of the oncogenically relevant target genes that respond to Jun and Fos.
引用
收藏
页码:1799 / 1809
页数:11
相关论文
共 65 条
  • [1] COGNATE DNA-BINDING SPECIFICITY RETAINED AFTER LEUCINE ZIPPER EXCHANGE BETWEEN GCN4 AND C/EBP
    AGRE, P
    JOHNSON, PF
    MCKNIGHT, SL
    [J]. SCIENCE, 1989, 246 (4932) : 922 - 926
  • [2] THE TRANSACTIVATING DOMAIN OF THE C-JUN PROTO-ONCOPROTEIN IS REQUIRED FOR COTRANSFORMATION OF RAT EMBRYO CELLS
    ALANI, R
    BROWN, P
    BINETRUY, B
    DOSAKA, H
    ROSENBERG, RK
    ANGEL, P
    KARIN, M
    BIRRER, MJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) : 6286 - 6295
  • [3] THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1
    ANGEL, P
    HATTORI, K
    SMEAL, T
    KARIN, M
    [J]. CELL, 1988, 55 (05) : 875 - 885
  • [4] ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1
    ANGEL, P
    ALLEGRETTO, EA
    OKINO, ST
    HATTORI, K
    BOYLE, WJ
    HUNTER, T
    KARIN, M
    [J]. NATURE, 1988, 332 (6160) : 166 - 171
  • [5] PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR
    ANGEL, P
    IMAGAWA, M
    CHIU, R
    STEIN, B
    IMBRA, RJ
    RAHMSDORF, HJ
    JONAT, C
    HERRLICH, P
    KARIN, M
    [J]. CELL, 1987, 49 (06) : 729 - 739
  • [6] CONTROL OF C-JUN ACTIVITY BY INTERACTION OF A CELL-SPECIFIC INHIBITOR WITH REGULATORY DOMAIN-DELTA - DIFFERENCES BETWEEN V-JUN AND C-JUN
    BAICHWAL, VR
    TJIAN, R
    [J]. CELL, 1990, 63 (04) : 815 - 825
  • [7] FUNCTIONAL ANTAGONISM BETWEEN C-JUN AND MYOD PROTEINS - A DIRECT PHYSICAL ASSOCIATION
    BENGAL, E
    RANSONE, L
    SCHARFMANN, R
    DWARKI, VJ
    TAPSCOTT, SJ
    WEINTRAUB, H
    VERMA, IM
    [J]. CELL, 1992, 68 (03) : 507 - 519
  • [8] HA-RAS AUGMENTS C-JUN ACTIVITY AND STIMULATES PHOSPHORYLATION OF ITS ACTIVATION DOMAIN
    BINETRUY, B
    SMEAL, T
    KARIN, M
    [J]. NATURE, 1991, 351 (6322) : 122 - 127
  • [9] HUMAN PROTOONCOGENE C-JUN ENCODES A DNA-BINDING PROTEIN WITH STRUCTURAL AND FUNCTIONAL-PROPERTIES OF TRANSCRIPTION FACTOR AP-1
    BOHMANN, D
    BOS, TJ
    ADMON, A
    NISHIMURA, T
    VOGT, PK
    TJIAN, R
    [J]. SCIENCE, 1987, 238 (4832) : 1386 - 1392
  • [10] BIOCHEMICAL-ANALYSIS OF TRANSCRIPTIONAL ACTIVATION BY JUN - DIFFERENTIAL ACTIVITY OF C-JUN AND V-JUN
    BOHMANN, D
    TJIAN, R
    [J]. CELL, 1989, 59 (04) : 709 - 717