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Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected

IsK is a K+ channel of the delayed rectifier type widely distributed throughout both excitable and nonexcitable cells. Its structure is different from other cloned K+ channels and molecular details of its gating remain obscure. Here we show that the activation kinetics of IsK expressed in Xenopus oo...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2229196/
https://www.ncbi.nlm.nih.gov/pubmed/7964597
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collection PubMed
description IsK is a K+ channel of the delayed rectifier type widely distributed throughout both excitable and nonexcitable cells. Its structure is different from other cloned K+ channels and molecular details of its gating remain obscure. Here we show that the activation kinetics of IsK expressed in Xenopus oocytes depend upon the amount of its mRNA injected, with larger amounts resulting in slower activation kinetics with a longer initial delay during activation. Similar changes in activation kinetics occur with time after a single injection of IsK mRNA. We present two kinetic schemes which illustrate how our experimental results could arise. Both imply an interaction among individual channel proteins during IsK activation. The dependence of channel gating on mRNA concentration provides a novel mechanism for long term regulation of ion current kinetics.
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spelling pubmed-22291962008-04-23 Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected J Gen Physiol Articles IsK is a K+ channel of the delayed rectifier type widely distributed throughout both excitable and nonexcitable cells. Its structure is different from other cloned K+ channels and molecular details of its gating remain obscure. Here we show that the activation kinetics of IsK expressed in Xenopus oocytes depend upon the amount of its mRNA injected, with larger amounts resulting in slower activation kinetics with a longer initial delay during activation. Similar changes in activation kinetics occur with time after a single injection of IsK mRNA. We present two kinetic schemes which illustrate how our experimental results could arise. Both imply an interaction among individual channel proteins during IsK activation. The dependence of channel gating on mRNA concentration provides a novel mechanism for long term regulation of ion current kinetics. The Rockefeller University Press 1994-07-01 /pmc/articles/PMC2229196/ /pubmed/7964597 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title_full Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title_fullStr Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title_full_unstemmed Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title_short Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected
title_sort gating of isk expressed in xenopus oocytes depends on the amount of mrna injected
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2229196/
https://www.ncbi.nlm.nih.gov/pubmed/7964597