Abstract
We have isolated a novel variant form of GIRK2, designated GIRK2B, from mouse brain cDNA library. GIRK2B was much shorter than the first type of GIRK2 (GIRK2A), but its amino acid sequence was identical to the corresponding part of GIRK2A except the C-terminal eight amino acid residues. When GIRK2B cRNA was co-injected with GIRK1 and m2-receptor cRNAs to Xenopus oocytes, acetylcholine-induction of the inwardly rectifying K+ current was enhanced dramatically. This suggests that GIRK2B can form a heteromultimeric G-protein-gated K+ channel with GIRK1. The reverse transcription polymerase chain reaction analysis showed that GIRK2B mRNA distributed much more broadly than GIRK1 mRNA. Therefore, GIRK2B might also play other unrecognized roles in various tissues than to form a K+ channel with GIRK1.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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Brain / metabolism
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DNA Primers
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DNA, Complementary
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Female
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G Protein-Coupled Inwardly-Rectifying Potassium Channels
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Gene Expression*
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Gene Library
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Genetic Variation
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Mice
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Molecular Sequence Data
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Oocytes / physiology*
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Polymerase Chain Reaction
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Potassium Channels / biosynthesis*
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Potassium Channels / physiology*
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Potassium Channels, Inwardly Rectifying*
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RNA, Messenger / analysis
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RNA, Messenger / biosynthesis
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Recombinant Proteins / biosynthesis
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Recombinant Proteins / metabolism
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Sequence Homology, Amino Acid
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Xenopus
Substances
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DNA Primers
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DNA, Complementary
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G Protein-Coupled Inwardly-Rectifying Potassium Channels
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Potassium Channels
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Potassium Channels, Inwardly Rectifying
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RNA, Messenger
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Recombinant Proteins