A novel distal enhancer confers chorionic expression on the human renin gene

被引:43
|
作者
Germain, S
Bonnet, F
Philippe, J
Fuchs, S
Corvol, P
Pinet, F
机构
[1] Coll France, F-75005 Paris, France
[2] INSERM, U36, F-75005 Paris, France
关键词
D O I
10.1074/jbc.273.39.25292
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
Renin catalyzes the rate-limiting step of the renin-angiotensin system, which regulates blood pressure and electrolyte homeostasis. To determine cell-specific human renin gene control elements, the transcriptional activity of promoter regions up to position -8876 was studied in renin-expressing cells. A positive regulatory region conferring similar to 57-fold higher transcriptional activity to the human renin gene promoter in chorionic cells was identified between nucleotides -5777 and -5552, It had the orientation-independent activity typical of classical enhancers. It also conferred similar to 59-fold higher transcriptional levels from the heterologous simian virus 40 (SV40) promoter in chorionic cells and similar to 6-fold higher transcriptional levels in Calu-6 and As4.1 cells, whereas no effect was measured in non-renin-expressing cells. DNase I footprinting showed that this enhancer contains three binding sites for chorionic cell nuclear extracts. Functional analysis suggested that the activity of the enhancer is regulated by differential mechanisms in the three renin-expressing cells involving a complex arrangement of AP-1 motifs binding cell-specific members of the basic leucine zipper family of transcription factors. Thus, our results demonstrate that this enhancer plays a key role in the expression of the human renin gene in the chorion and may also be involved in its regulated expression in other tissues.
引用
收藏
页码:25292 / 25300
页数:9
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