Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)

被引:102
作者
Mastroianni, N
DeFusco, M
Zollo, M
Arrigo, G
Zuffardi, O
Bettinelli, A
Ballabio, A
Casari, G
机构
[1] TELETHON INST GENET & MED TIGEM,I-20132 MILAN,ITALY
[2] UNIV MILAN,CLIN PEDIAT 2,I-20122 MILAN,ITALY
[3] HOSP SAN RAFFAELE,LAB CITOGENET,I-20132 MILAN,ITALY
[4] IST BIOL GEN & GENET MED,PAVIA,ITALY
[5] UNIV SIENA,DEPT MOL BIOL,I-53100 SIENA,ITALY
关键词
D O I
10.1006/geno.1996.0388
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Electrolyte homeostasis is maintained by several ion transport systems. Na-(K)-Cl cotransporters promote the electrically silent movement of chloride across the membrane in absorptive and secretory epithelia. Two kidney-specific Na-(K)-Cl cotransporter isoforms are known, so far, according to their sensitivity to specific inhibitors, We have cloned the human cDNA coding for the renal Na-Cl cotransporter selectively inhibited by the thiazide class of diuretic agents. The predicted protein sequence of 1021 amino acids (112 kDa) shows a structure common to the other members of the Na-(K)-Cl cotransporter family: a central region harboring 12 transmembrane domains and the 2 intracellular hydrophilic amino and carboxyl termini. The expression pattern of the human Na-Cl thiazide-sensitive cotransporter (hTSC, HGMW-approved symbol SLC12A3) confirms the kidney specificity. hTSC has been mapped to human chromosome 16q13 by fluorescence in situ hybridization. The cloning and characterization of hTSC now render it possible to study the involvement of this cotransport system in the pathogenesis of tubulopathies such as Gitelman syndrome. (C) 1996 Academic Press, Inc.
引用
收藏
页码:486 / 493
页数:8
相关论文
共 26 条
[1]   USE OF CALCIUM EXCRETION VALUES TO DISTINGUISH 2 FORMS OF PRIMARY RENAL TUBULAR HYPOKALEMIC ALKALOSIS - BARTTER AND GITELMAN SYNDROMES [J].
BETTINELLI, A ;
BIANCHETTI, MG ;
GIRARDIN, E ;
CARINGELLA, A ;
CECCONI, M ;
APPIANI, AC ;
PAVANELLO, L ;
GASTALDI, R ;
ISIMBALDI, C ;
LAMA, G ;
MARCHESONI, C ;
MATTEUCCI, C ;
PATRIARCA, P ;
DINATALE, B ;
SETZU, C ;
VITUCCI, P .
JOURNAL OF PEDIATRICS, 1992, 120 (01) :38-43
[2]   MOLECULAR MECHANISMS OF DIURETIC AGENTS [J].
BREYER, J ;
JACOBSON, HR .
ANNUAL REVIEW OF MEDICINE, 1990, 41 :265-275
[3]  
DELPIRE E, 1994, J BIOL CHEM, V269, P25677
[4]   IMMUNOCYTOCHEMICAL CHARACTERIZATION OF THE HIGH-AFFINITY THIAZIDE DIURETIC RECEPTOR IN RABBIT RENAL-CORTEX [J].
ELLISON, DH ;
BIEMESDERFER, D ;
MORRISEY, J ;
LAURING, J ;
DESIR, GV .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (01) :F141-F148
[5]   PROGRESSIVE SEQUENCE ALIGNMENT AS A PREREQUISITE TO CORRECT PHYLOGENETIC TREES [J].
FENG, DF ;
DOOLITTLE, RF .
JOURNAL OF MOLECULAR EVOLUTION, 1987, 25 (04) :351-360
[6]  
FORBUSH B, 1983, J BIOL CHEM, V258, P1787
[7]   PRIMARY STRUCTURE AND FUNCTIONAL EXPRESSION OF A CDNA-ENCODING THE THIAZIDE-SENSITIVE, ELECTRONEUTRAL SODIUM-CHLORIDE COTRANSPORTER [J].
GAMBA, G ;
SALTZBERG, SN ;
LOMBARDI, M ;
MIYANOSHITA, A ;
LYTTON, J ;
HEDIGER, MA ;
BRENNER, BM ;
HEBERT, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2749-2753
[8]  
GAMBA G, 1994, J BIOL CHEM, V269, P17713
[9]  
Gitelman H J, 1966, Trans Assoc Am Physicians, V79, P221
[10]  
GLASS DB, 1986, J BIOL CHEM, V261, P2987