Dang J, Boyd D, Wang H, Allgayer H, Doe W F, Wang Y
Division of Molecular Medicine, John Curtin School of Medical Research, The Australian National University, Canberra.
Eur J Biochem. 1999 Aug;264(1):92-9. doi: 10.1046/j.1432-1327.1999.00583.x.
An 8.5-kb 5'-flanking region of the human urokinase-type plasminogen activator receptor (uPAR) gene was cloned and the detailed uPAR promoter region defined in an 188-bp fragment between bases -141 and +47 relative to the transcription-start site. 5'-Deletion to -100 and -60 in the region abolished its promoter activity, indicating that an 81-bp segment between -141 and -61, which contains a proximal AP-1 site at position -70, is required for uPAR promoter activity. Nuclear extracts from HCT116 cells contain proteins that specifically bind to the AP-1 site. Mutation of the AP-1 motif reduced uPAR promoter activity in comparison with the wild-types. Induction of uPAR expression by phorbol ester requires this AP-1 motif in colon cancer cells. Cotransfection with the c-jun and c-fos expression vectors stimulated the uPAR promoter activity four- to fivefold. These results demonstrate that the proximal AP-1 motif is responsible for approximately 50% of the basal expression of the uPAR gene.
克隆了人尿激酶型纤溶酶原激活剂受体(uPAR)基因8.5 kb的5'-侧翼区域,并在相对于转录起始位点-141至+47碱基之间的188 bp片段中确定了详细的uPAR启动子区域。该区域5'-缺失至-100和-60会消除其启动子活性,表明-141至-61之间的81 bp片段是uPAR启动子活性所必需的,该片段在-70位含有一个近端AP-1位点。HCT116细胞的核提取物含有能特异性结合AP-1位点的蛋白质。与野生型相比,AP-1基序的突变降低了uPAR启动子活性。佛波酯诱导结肠癌细胞中uPAR表达需要该AP-1基序。与c-jun和c-fos表达载体共转染可刺激uPAR启动子活性提高4至5倍。这些结果表明,近端AP-1基序约占uPAR基因基础表达的50%。