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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Davidson, N. Lester, H. A. Kofuji, P. |
| Description | Author Affiliation: Kofuji P ( Division of Biology, California Institute of Technology, Pasadena 91225, USA.); |
| Abstract | Guanine nucleotide-binding proteins (G proteins) activate K+ conductances in cardiac atrial cells to slow heart rate and in neurons to decrease excitability. cDNAs encoding three isoforms of a G-protein-coupled, inwardly rectifying K+ channel (GIRK) have recently been cloned from cardiac (GIRK1/Kir 3.1) and brain cDNA libraries (GIRK2/Kir 3.2 and GIRK3/Kir 3.3). Here we report that GIRK2 but not GIRK3 can be activated by G protein subunits G beta 1 and G gamma 2 in Xenopus oocytes. Furthermore, when either GIRK3 or GIRK2 was coexpressed with GIRK1 and activated either by muscarinic receptors or by G beta gamma subunits, G-protein-mediated inward currents were increased by 5- to 40-fold. The single-channel conductance for GIRK1 plus GIRK2 coexpression was intermediate between those for GIRK1 alone and for GIRK2 alone, and voltage-jump kinetics for the coexpressed channels displayed new kinetic properties. On the other hand, coexpression of GIRK3 with GIRK2 suppressed the GIRK2 alone response. These studies suggest that formation of heteromultimers involving the several GIRKs is an important mechanism for generating diversity in expression level and function of neurotransmitter-coupled, inward rectifier K+ channels. |
| ISSN | 00278424 |
| e-ISSN | 10916490 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Issue Number | 14 |
| Volume Number | 92 |
| Language | English |
| Publisher | National Academy of Sciences |
| Publisher Date | 1995-08-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Brain Physiology GTP-Binding Proteins Neurons Potassium Channels, Inwardly Rectifying Potassium Channels Acetylcholine Pharmacology Animals Metabolism Cloning, Molecular Evoked Potentials G Protein-Coupled Inwardly-Rectifying Potassium Channels Heart Macromolecular Substances Membrane Potentials Drug Effects Mice Myocardium Oocytes Patch-Clamp Techniques Potassium Biosynthesis RNA, Complementary Receptors, Muscarinic Xenopus Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
| Subject | Multidisciplinary |
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