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      THIK-1 and THIK-2, a novel subfamily of tandem pore domain K+ channels.

      The Journal of Biological Chemistry
      Amino Acid Sequence, Anesthetics, Inhalation, pharmacology, Animals, Anions, Arachidonic Acid, Base Sequence, Brain, metabolism, Chromosome Mapping, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 2, Cloning, Molecular, DNA, Complementary, Electrophysiology, Green Fluorescent Proteins, Halothane, Humans, Hydrogen-Ion Concentration, In Situ Hybridization, Introns, Kidney, Liver, Luminescent Proteins, Microscopy, Confocal, Molecular Sequence Data, Phylogeny, Potassium, Potassium Channels, biosynthesis, chemistry, genetics, Potassium Channels, Tandem Pore Domain, Rats, Recombinant Proteins, Reverse Transcriptase Polymerase Chain Reaction, Sequence Homology, Amino Acid, Stomach, Tissue Distribution, Xenopus

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          Abstract

          Two cDNAs encoding novel K(+) channels, THIK-1 and THIK-2 (tandem pore domain halothane inhibited K(+) channel), were isolated from rat brain. The proteins of 405 and 430 amino acids were 58% identical to each other. Homology analysis showed that the novel channels form a separate subfamily among tandem pore domain K(+) channels. The genes of the human orthologs were identified as human genomic data base entries. They possess one intron each and were assigned to chromosomal region 14q24.1-14q24.3 (human (h) THIK-1) and 2p22-2p21 (hTHIK-2). In rat (r), THIK-1 (rTHIK-1) is expressed ubiquitously; rTHIK-2 expression was found in several tissues including brain and kidney. In situ hybridization of brain slices showed that rTHIK-2 is strongly expressed in most brain regions, whereas rTHIK-1 expression is more restricted. Heterologous expression of rTHIK-1 in Xenopus oocytes revealed a K(+) channel displaying weak inward rectification in symmetrical K(+) solution. The current was enhanced by arachidonic acid and inhibited by halothane. rTHIK-2 did not functionally express. Confocal microscopy of oocytes injected with green fluorescent protein-tagged rTHIK-1 or rTHIK-2 showed that both channel subunits are targeted to the outer membrane. However, coinjection of rTHIK-2 did not affect the currents induced by rTHIK-1, indicating that the two channel subunits do not form heteromers.

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