A SP1 BINDING-SITE IN THE GC-RICH REGION IS ESSENTIAL FOR A CORE PROMOTER ACTIVITY OF THE HUMAN ENDOTHELIAL NITRIC-OXIDE SYNTHASE GENE

被引:39
作者
WARIISHI, S
MIYAHARA, K
TODA, K
OGOSHI, S
DOI, Y
OHNISHI, S
MITSUI, Y
YUI, Y
KAWAI, C
SHIZUTA, Y
机构
[1] KOCHI MED SCH,DEPT MED CHEM,NANKO KU,KOCHI 783,JAPAN
[2] KOCHI MED SCH,DEPT SURG 2,NANKO KU,KOCHI 783,JAPAN
[3] KOCHI MED SCH,DEPT GERIATR MED,NANKO KU,KOCHI 783,JAPAN
[4] KOCHI MED SCH,DEPT INTERNAL MED,NANKO KU,KOCHI 783,JAPAN
[5] NATL INST BIOSCI & HUMAN TECHNOL,AGCY IND SCI & TECHNOL,TSUKUBA,IBARAKI 305,JAPAN
[6] KYOTO UNIV,FAC MED,DEPT INTERNAL MED,KYOTO 606,JAPAN
关键词
D O I
10.1006/bbrc.1995.2682
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
Endothelial nitric oxide synthase (eNOS) is an important oxygenase which catalyzes the conversion of L-arginine to L-citrulline to form nitric oxide (NO), a potent important factor for vasodilation and inhibition of platelet aggregation. We have analyzed characteristics of the promoter region of the human eNOS gene using the transient expression in human endothelial cells of CAT constructs with a series of 5'-deletion mutants. The 5'-flanking region between -116 and -98, which contains a putative consensus sequence for binding of transcription factor Spl, is essential to direct a basal promoter activity. Gel mobility shift analysis involving anti-Spl antibody and competitor DNAs disrupted at the binding site for Spl reveals that Spl or its closely related protein(s) binds to the consensus sequence located between -104 and -96. These results indicate that the Spl site is essential for a core promoter activity of the human eNOS gene. (C) 1995 Press, Inc.
引用
收藏
页码:729 / 735
页数:7
相关论文
共 42 条
[1]  
ASANO K, 1994, P NATL ACAD SCI US 9, P10089
[2]   INCREASED EXPRESSION AND DNA-BINDING ACTIVITY OF TRANSCRIPTION FACTOR SP1 IN DOXORUBICIN-RESISTANT HL-60 LEUKEMIA-CELLS [J].
BORELLINI, F ;
AQUINO, A ;
JOSEPHS, SF ;
GLAZER, RI .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5541-5547
[3]  
CHARTRAIN NA, 1994, J BIOL CHEM, V269, P6765
[4]  
CORNWELL MM, 1993, J BIOL CHEM, V268, P19505
[5]   MEMBERS OF THE SP TRANSCRIPTION FACTOR FAMILY CONTROL TRANSCRIPTION FROM THE UTEROGLOBIN PROMOTER [J].
DENNIG, J ;
HAGEN, G ;
BEATO, M ;
SUSKE, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (21) :12737-12744
[6]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[7]   ISOLATION OF TRANSCRIPTION FACTORS THAT DISCRIMINATE BETWEEN DIFFERENT PROMOTERS RECOGNIZED BY RNA POLYMERASE-II [J].
DYNAN, WS ;
TJIAN, R .
CELL, 1983, 32 (03) :669-680
[8]   ENDOTHELIUM-DERIVED RELAXING AND CONTRACTING FACTORS [J].
FURCHGOTT, RF ;
VANHOUTTE, PM .
FASEB JOURNAL, 1989, 3 (09) :2007-2018
[9]   REGULATION OF THE TRANSFORMING GROWTH-FACTOR-BETA-1 AND FACTOR-BETA-3 PROMOTERS BY TRANSCRIPTION FACTOR SP1 [J].
GEISER, AG ;
BUSAM, KJ ;
KIM, SJ ;
LAFYATIS, R ;
OREILLY, MA ;
WEBBINK, R ;
ROBERTS, AB ;
SPORN, MB .
GENE, 1993, 129 (02) :223-228
[10]   IDENTIFICATION OF REGULATORY SEQUENCES IN THE PRELUDE SEQUENCES OF AN H2A HISTONE GENE BY THE STUDY OF SPECIFIC DELETION MUTANTS INVIVO [J].
GROSSCHEDL, R ;
BIRNSTIEL, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (03) :1432-1436