Repression by homeoprotein Pitx1 of virus-induced interferon a promoters is mediated by physical interaction and trans repression of IRF3 and IRF7

被引:19
作者
Island, ML
Mesplede, T
Darracq, N
Bandu, MT
Christeff, N
Djian, P
Drouin, J
Navarro, S
机构
[1] Univ Paris 05, CNRS, UPR 2228,UFR Biomed St Peres, Lab Reg Transcript & Malad Genet, F-75270 Paris 06, France
[2] Inst Rech Clin Montreal, Mol Genet Lab, Montreal, PQ H2W 1R7, Canada
关键词
D O I
10.1128/MCB.22.20.7120-7133.2002
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
Interferon A (IFN-A) genes are differentially expressed after virus induction. The differential expression of individual IFN-A genes is modulated by the specific transcription activators IFN regulatory factor 3 (IRF3) and IRF-7 and the homeoprotein transcription repressor Pitx1. We now show that repression by Pitx1 does not appear to be due to the recruitment of histone deacetylases. On the other hand, Pitx1 inhibits the IRF3 and IRF7 transcriptional activity of the IFN-Al1 and IFN-A5 promoters and interacts physically with IRF3 and IRF7. Pitx1 trans-repression activity maps to specific C-terminal domains, and the Pitx1 homeodomain is involved in physical interaction with IRF3 or IRF7. IRF3 is able to bind to the antisilencer region of the IFN-A4 promoter, which overrides the repressive activity of Pitx1. These results indicate that interaction between the Pitx1 homeodomain and IRF3 or IRF7 and the ability of the Pitx1 C-terminal repressor domains to block IFN-Al1 and IFN-A5 but not IFN-A4 promoter activities may contribute to our understanding of the complex differential transcriptional activation, repression, and antirepression of the IFN-A genes.
引用
收藏
页码:7120 / 7133
页数:14
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