Repression of virus-induced interferon A promoters by homeodomain transcription factor Ptx1

被引:18
作者
Lopez, SB
Island, ML
Drouin, J
Bandu, MT
Christeff, N
Darracq, N
Barbey, R
Doly, J
Thomas, D
Navarro, S
机构
[1] Univ Paris 05, UFR Biomed St Peres, Lab Regulat Transcript & Malad Genet, CNRS,UPR 2228, F-75270 Paris 06, France
[2] Inst Rech Clin Montreal, Genet Mol Lab, Montreal, PQ H2W 1R7, Canada
[3] CNRS, Ctr Genet Mol, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1128/MCB.20.20.7527-7540.2000
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 substitutions in the proximal positive virus responsive element A (VRE-A) of their promoters and by the presence or absence of a distal negative regulatory element (DNRE). The functional feature of the DNRE is to specifically act by repression of VRE-A activity. With the use of the yeast one-hybrid system, we describe here the identification of a specific DNRE-binding protein, the pituitary homeobox 1 (Ptx1 or Pitx1), Ptx1 is detectable in different cell types that differentially express IFN-A genes, and the endogenous Ptx1 protein binds specifically to the DNRE. Upon virus induction, Ptx1 negatively regulates the transcription of DNRE-containing IFN-A promoters, and the C-terminal region, as well as the homeodomain of the Ptx1 protein, is required for this repression. After virus induction, the expression of the Ptx1 antisense RNA leads to a significant increase of endogenous IFN-A gene transcription and is able to modify the pattern of differential expression of individual IFN-A genes. These studies suggest that Ptx1 contributes to the differential transcriptional strength of the promoters of different IFN-A genes and that these genes may provide new targets for transcriptional regulation by a homeodomain transcription factor.
引用
收藏
页码:7527 / 7540
页数:14
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