Abstract
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 ≃50% of the basal expression of the uPAR gene.
Original language | English |
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Pages (from-to) | 92-99 |
Number of pages | 8 |
Journal | European Journal of Biochemistry |
Volume | 264 |
Issue number | 1 |
DOIs | |
Publication status | Published - 15 Aug 1999 |