A CONSERVED TATA-LESS PROXIMAL PROMOTER DRIVES BASAL TRANSCRIPTION FROM THE UROKINASE-TYPE PLASMINOGEN-ACTIVATOR RECEPTOR GENE

被引:75
作者
SORAVIA, E
GREBE, A
DELUCA, P
HELIN, K
SUH, TT
DEGEN, JL
BLASI, F
机构
[1] UNIV MILAN,DEPT GENET & MICROBIOL,MILAN,ITALY
[2] UNIV COPENHAGEN,DEPT MOLEC CELL BIOL,COPENHAGEN,DENMARK
[3] UNIV NAPLES,DEPT GENET & MOLEC BIOL,NAPLES,ITALY
[4] DANISH CANC SOC,DIV CANC BIOL,COPENHAGEN,DENMARK
[5] CHILDRENS HOSP,MED CTR TCHRF,CHILDRENS HOSP RES FDN,CINCINNATI,OH
关键词
D O I
10.1182/blood.V86.2.624.bloodjournal862624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The urohinase-type plasminogen activator receptor (uPAR) focuses at the cell surface the activation of pro-uPA and, hence, the formation of plasmin, thus enhancing directional extracellular proteolysis. To characterize the transcriptional regulatory mechanisms that control receptor expression, we have cloned an uPAR DNA segment containing upstream regulatory sequences from both the human and murine genomes. We report that a proximal promoter, contained within 180 bp from the major transcription start sites of the human uPAR gene, drives basal transcription. This region lacks TATA and CAAT boxes and contains relatively GC-rich proximal sequences. A subregion of this sequence, highly conserved between human and murine genes, contains most of the promoter activity and is specifically bound by Hela nuclear proteins, one of which belongs to the SP1 class. (C) 1995 by The American Society of Hematology.
引用
收藏
页码:624 / 635
页数:12
相关论文
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