Cloning and kidney cell-specific activity of the promoter of the murine renal Na-K-Cl cotransporter gene

被引:90
作者
Igarashi, P
Whyte, DA
Li, K
Nagami, GT
机构
[1] YALE UNIV,SCH MED,DEPT PEDIAT,NEW HAVEN,CT 06520
[2] W LOS ANGELES DEPT VET AFFAIRS,MED CTR,MED & RES SERV,LOS ANGELES,CA 90073
关键词
D O I
10.1074/jbc.271.16.9666
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
The murine Nkcc2/Slc12a1 gene encodes a bumetanide sensitive Na-K-Cl cotransporter that is expressed exclusively in the kidney in the thick ascending limb of the loop of Henle, Nuclear run-off assays demonstrated that kidney-specific expression of Nkcc2 was due, at least in part, to kidney-specific gene transcription, To begin study of the gene promoter, a genomic clone that contained 13.5 kilobases of the 5'-flanking region of Nkcc2 was isolated. A single transcription initiation site was located 1330 base pairs (bp) upstream of the start codon. The sequence of the proximal 5'-flanking region contained typical eukaryotic promoter elements including a TATA box, two CCAAT boxes, and an initiator, A (G-A)(28) (C-T)(28) microsatellite and consensus binding sites for hepatocyte nuclear factor 1, cAMP-response element binding protein, CCAAT/enhancer-binding proteins, and basic helix-loop-helix proteins, were also identified, To functionally express the promoter, 2255 bp of the proximal 5'-flanking region was ligated to a luciferase reporter gene and transfected into thick ascending limb (TAL) cells, a stable cell line derived from microdissected loops of Henle of the Tg(SV40E)Bri7 mouse. TAL cells exhibited furosemide-sensitive Na-K(NH4+)-Cl cotransport activity and endogenously expressed the 5.0-kilobase Nkcc2 transcript. Luciferase activity was 130-fold greater following transfection into TAL cells compared with transfection into cells that did not express Nkcc2 (NIH 3T3 fibroblasts). Deletion analysis revealed that promoter activity in TAL cells was similar in constructs extending from the transcription initiation site to -1529 to -469, whereas further deletion to -190 resulted in a 76% decrease in activity, We conclude that the Nkcc2 promoter exhibits kidney cell-specific activity. Regulatory elements required for maximal promoter activity are located in a 280-bp DNA segment that contains consensus binding sites for several transcription factors expressed in the kidney.
引用
收藏
页码:9666 / 9674
页数:9
相关论文
共 43 条
[1]  
[Anonymous], TRANSCRIPTIONAL REGU
[2]   CELL-SPECIFIC EXPRESSION OF CYTOSOLIC PHOSPHOENOLPYRUVATE CARBOXYKINASE IN TRANSGENIC MICE [J].
BEALE, EG ;
CLOUTHIER, DE ;
HAMMER, RE .
FASEB JOURNAL, 1992, 6 (15) :3330-3337
[3]   PHYLOGENETICALLY CONSERVED SEQUENCES IN THE PROMOTER OF THE RABBIT SODIUM-HYDROGEN EXCHANGER ISOFORM-1 GENE (NHE1/SLC9A1) [J].
BLAUROCK, MC ;
REBOUCAS, NA ;
KUSNEZOV, JL ;
IGARASHI, P .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1995, 1262 (2-3) :159-163
[4]  
CELANO P, 1989, BIOTECHNIQUES, V7, P942
[5]  
DELPIRE E, 1994, J BIOL CHEM, V269, P25677
[6]   SITE-DIRECTED MUTAGENESIS OF VIRTUALLY ANY PLASMID BY ELIMINATING A UNIQUE SITE [J].
DENG, WP ;
NICKOLOFF, JA .
ANALYTICAL BIOCHEMISTRY, 1992, 200 (01) :81-88
[7]   EXPRESSION OF THE HELIX-LOOP-HELIX PROTEIN, ID, DURING BRANCHING MORPHOGENESIS IN THE KIDNEY [J].
DUNCAN, MK ;
SHIMAMURA, T ;
CHADA, K .
KIDNEY INTERNATIONAL, 1994, 46 (02) :324-332
[8]   COMPILATION OF VERTEBRATE-ENCODED TRANSCRIPTION FACTORS [J].
FAISST, S ;
MEYER, S .
NUCLEIC ACIDS RESEARCH, 1992, 20 (01) :3-26
[9]  
GAGNON ML, 1992, DEVELOPMENT, V114, P457
[10]  
GAMBA G, 1994, J BIOL CHEM, V269, P17713