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Cloning of a pH-sensitive K+ channel possessing two transmembrane segments Makoto Suzuki*, Keiko Takahashi, Masato Ikeda, Hiroshi Hayakawa, Aiichirou Ogawa, Yoshindo Kawaguchi & Osamu Sakai
*Department of Pharmacology, Jichi Medical School, 3311-1, Minamikawachi, Kawachi, Tochigi 329-04, Japan Internal Medicine II, Jikeikai University School of Medicine, 3-19-18, Nishishinbashi, Minatoku, Tokyo 105, Japan
THE mammalian renal collecting ducts are responsible for secreting potassium ions into the urine and are a major regulatory site for potassium homeostasis1, in which a voltage-independent pH-sensitive K+ channel in the apical membrane plays a central role2,3. Here we describe a complementary DNA encoding a novel K+ channel from rabbit renal cortical collecting tubule cells (RACTK1). RACTK1 has the functional characteristics of the apical K+-permeable channel and consists of 284 amino acids, putatively with two transmembrane segments. The sequence of RACTK1, however, shows no homology to known voltage-dependent or -independent K+ channels, and has a different K+-driving path and regulatory sites. The study of this protein should provide insight into K+ homeostasis and diseases of K+ metabolism.
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