CONTROL OF C-JUN ACTIVITY BY INTERACTION OF A CELL-SPECIFIC INHIBITOR WITH REGULATORY DOMAIN-DELTA - DIFFERENCES BETWEEN V-JUN AND C-JUN

被引:216
作者
BAICHWAL, VR [1 ]
TJIAN, R [1 ]
机构
[1] UNIV CALIF BERKELEY, DEPT MOLEC & CELLULAR BIOL, BERKELEY, CA 94720 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0092-8674(90)90147-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Analysis of transcriptional activation properties of c-Jun chimeras in different cell lines suggests that it contains an activator domain (A1) that is negatively regulated by a cell type-specific inhibitor. A regulatory domain of c-Jun, δ, previously identified by in vitro experiments, also regulates transcriptional activation by c-Jun in vivo. The δ domain facilitates or stabilizes the interaction of the cellular inhibitor with A1. v-Jun, which lacks δ, is a stronger transcriptional activator than c-Jun, since its activity is not efficiently repressed by the cellular inhibitor. In vitro transcription with chimeric Jun proteins and extracts from different cell types confirms that the A1 and δ domains are repressed in a cell type-specific manner. These findings implicate a specific cellular factor in the negative regulation of c-Jun activity and suggest a molecular basis for the observed difference in transcriptional properties between v-Jun and c-Jun. © 1990.
引用
收藏
页码:815 / 825
页数:11
相关论文
共 49 条
  • [1] Abel, Maniatis, Action of leucine zippers, Nature, 341, pp. 24-25, (1989)
  • [2] Angel, Imagawa, Chiu, Stein, Imbra, Rahmsdorf, Jonat, Herrlich, Karin, Phorbol ester-inducible genes contain a common cis element recognized by a TPA-modulated trans-acting factor, Cell, 49, pp. 729-739, (1987)
  • [3] Angel, Allegreto, Okino, Hattori, Boyle, Hunter, Karin, Oncogene jun encodes a sequence-specific trans-activator similar to AP-1, Nature, 322, pp. 166-170, (1988)
  • [4] Angel, Hattori, Smeal, Karin, The jun protoncogene is positively autoregulated by its product Jun/AP-1, Cell, 55, pp. 875-885, (1988)
  • [5] Angel, Smeal, Meek, Karin, jun and v-jun contain multiple regions that participate in transcriptional activation in an interdependent manner, New Biologist, 1, pp. 35-43, (1989)
  • [6] Bohmann, Tjian, Biochemical analysis of transcriptional activation by Jun: differential activity of c- and v-Jun, Cell, 59, pp. 709-717, (1989)
  • [7] Bohmann, Bos, Admon, Nishimura, Su, Vogt, Tjian, Human proto-oncogene c-jun encodes a DNA binding protein with structural and functional properties of transcription factor AP-1, Science, 238, pp. 1386-1392, (1987)
  • [8] Bos, Monteclaro, Mitsunobu, Ball, Chang, Nishimura, Vogt, Efficient transformation of chicken embryo fibroblasts by c-jun requires structural modification in coding and noncoding sequences, Genes Dev., 4, pp. 1677-1687, (1990)
  • [9] Carey, Kakidani, Leatherwood, Mostashari, Ptashne, An amino terminal fragment of GAL4 binds DNA as a dimer, J. Mol. Biol., 209, pp. 423-432, (1989)
  • [10] Chiu, Boyle, Meek, Smeal, Hunter, Karin, The c-Fos protein interacts with c-Jun/AP-1 to stimulate transcription of AP-1 responsive genes, Cell, 54, pp. 541-552, (1988)