A specific lysine in c-Jun is required for transcriptional repression by E1A and is acetylated by p300

被引:74
作者
Vries, RGJ [1 ]
Prudenziati, M [1 ]
Zwartjes, C [1 ]
Verlaan, M [1 ]
Kalkhoven, E [1 ]
Zantema, A [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2333 AL Leiden, Netherlands
关键词
acetylation; CBP; c-Jun; E1A; p300;
D O I
10.1093/emboj/20.21.6095
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
The adenovirus E1A protein regulates transcription of cellular genes via its interaction with the transcriptional coactivators p300/CBP. The collagenase promoter activated by the c-Jun protein is repressed by E1A. Here we show that E1A repression is specific for c-Jun, as E1A does not repress the collagenase promoter activated by the homologous transcription factor EB1. Using chimeras of c-Jun and EB1, we demonstrate that a 12 amino acid region in the basic region of the c-Jun DNA-binding domain is essential for repression by E1A. Since repression requires the binding of p300 to E1A, we studied the involvement of p300 acetyltransferase activity in the repression mechanism. We demonstrate that c-Jun is acetylated in vivo, and mutational analysis identified Lys271 in the c-Jun basic region to be essential for repression of the collagenase promoter by E1A. In addition, Lys271 is acetylated both in vitroandin vivo. These results suggest that the specific repression of the collagenase promoter by E1A involves acetylation of c-Jun.
引用
收藏
页码:6095 / 6103
页数:9
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