Cloning, characterization, and gene organization of K-Cl cotransporter from pig and human kidney and C-elegans

被引:61
作者
Holtzman, EJ
Kumar, S
Faaland, CA
Warner, F
Logue, PJ
Erickson, SJ
Ricken, G
Waldman, J
Kumar, S
Dunham, PB
机构
[1] SUNY Hlth Sci Ctr, Univ Hosp, Dept Med, Div Renal, Syracuse, NY 13210 USA
[2] SUNY Hlth Sci Ctr, Dept Biochem & Mol Biol, Syracuse, NY 13210 USA
[3] Syracuse Univ, Dept Biol, Syracuse, NY 13244 USA
关键词
inorganic ion cotransport; cell volume regulation; HEK cells; transient and stable transfection;
D O I
10.1152/ajprenal.1998.275.4.F550
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We isolated and characterized the cDNAs far the human, pig, and Caenorhabditis elegans K-CI cotransporters. The pig and human homologs are 94% identical and contain 1,085 and 1,086 amino acids, respectively. The deduced protein of the C. elegans K-CI cotransporter clone (CE-KCC1) contains 1,003 amino acids. The mammalian K-CI cotransporters share similar to 45% similarity with CE-KCC1. Hydropathy analyses of the three clones indicate typical KCC topology patterns with 12 transmembrane segments, large extracellular loops between transmembrane domains 5 and 6 (unique to KCC), and large COOH-terminal domains. Human KCC1 is widely expressed among various tissues. This KCC1 gene spans 23 kb and is organized in 24 exons, whereas the CE-KCC1 gene spans 3.5 kb and contains ID exons. Transiently and stably transfected human embryonic kidney cells (HEK-293) expressing the human, pig, and C. elegans K-Cl cotransporter fulfilled two (pig) or five (human and C. elegans) criteria for increased expression of the K-Cl cotransporter. The criteria employed were basal K-CI cotransport; stimulation of cotransport by swelling, N-ethylmaleimide, staurosporine, and reduced cell Mg concentration; and secondary stimulation of Na-K-CI cotransport.
引用
收藏
页码:F550 / F564
页数:15
相关论文
共 36 条
[31]   MOLECULAR-CLONING OF A PUTATIVE NA+-K+-2CL(-) COTRANSPORTER FROM THE MALPIGHIAN TUBULES OF THE TOBACCO HORNWORM, MANDUCA-SEXTA [J].
REAGAN, JD .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 25 (08) :875-880
[32]  
REUSS L, 1994, CELLULAR MOL PHYSL C, P31
[33]   Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter [J].
Simon, DB ;
NelsonWilliams, C ;
Bia, MJ ;
Ellison, D ;
Karet, FE ;
Molina, AM ;
Vaara, I ;
Iwata, F ;
Cushner, HM ;
Koolen, M ;
Gainza, FJ ;
Gitelman, HJ ;
Lifton, RP .
NATURE GENETICS, 1996, 12 (01) :24-30
[34]   Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2 [J].
Simon, DB ;
Karet, FE ;
Hamdan, JM ;
DiPietro, A ;
Sanjad, SA ;
Lifton, RP .
NATURE GENETICS, 1996, 13 (02) :183-188
[35]   2.2 MB OF CONTIGUOUS NUCLEOTIDE-SEQUENCE FROM CHROMOSOME-III OF C-ELEGANS [J].
WILSON, R ;
AINSCOUGH, R ;
ANDERSON, K ;
BAYNES, C ;
BERKS, M ;
BURTON, J ;
CONNELL, M ;
BONFIELD, J ;
COPSEY, T ;
COOPER, J ;
COULSON, A ;
CRAXTON, M ;
DEAR, S ;
DU, Z ;
DURBIN, R ;
FAVELLO, A ;
FRASER, A ;
FULTON, L ;
GARDNER, A ;
GREEN, P ;
HAWKINS, T ;
HILLIER, L ;
JIER, M ;
JOHNSTON, L ;
JONES, M ;
KERSHAW, J ;
KIRSTEN, J ;
LAISSTER, N ;
LATREILLE, P ;
LLOYD, C ;
MORTIMORE, B ;
OCALLAGHAN, M ;
PARSONS, J ;
PERCY, C ;
RIFKEN, L ;
ROOPRA, A ;
SAUNDERS, D ;
SHOWNKEEN, R ;
SIMS, M ;
SMALDON, N ;
SMITH, A ;
SMITH, M ;
SONNHAMMER, E ;
STADEN, R ;
SULSTON, J ;
THIERRYMIEG, J ;
THOMAS, K ;
VAUDIN, M ;
VAUGHAN, K ;
WATERSTON, R .
NATURE, 1994, 368 (6466) :32-38
[36]   MOLECULAR-CLONING AND FUNCTIONAL EXPRESSION OF THE BUMETANIDE-SENSITIVE NA-K-CL COTRANSPORTER [J].
XU, JC ;
LYTLE, C ;
ZHU, TT ;
PAYNE, JA ;
BENZ, E ;
FORBUSH, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2201-2205