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Am J Physiol Renal Physiol 275: F550-F564, 1998;
0363-6127/98 $5.00
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Vol. 275, Issue 4, F550-F564, October 1998

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

Eli J. Holtzman1,2, Sumit Kumar1, Carol A. Faaland1, Fern Warner1, Paul J. Logue3, Sara J. Erickson3, Gesa Ricken1, Jeremy Waldman1, Shiv Kumar1, and Philip B. Dunham3

1 Renal Division, Department of Medicine and 2 Department of Biochemistry and Molecular Biology, State University of New York-Health Science Center, Syracuse 13210; and 3 Department of Biology, Syracuse University, Syracuse, New York 13244

We isolated and characterized the cDNAs for the human, pig, and Caenorhabditis elegans K-Cl 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-Cl cotransporter clone (CE-KCC1) contains 1,003 amino acids. The mammalian K-Cl cotransporters share ~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 10 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-Cl cotransport; stimulation of cotransport by swelling, N-ethylmaleimide, staurosporine, and reduced cell Mg concentration; and secondary stimulation of Na-K-Cl cotransport.

inorganic ion cotransport; cell volume regulation; HEK cells; transient and stable transfection


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