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14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels
The ether-à-go-go (Eag) potassium (K(+)) channel belongs to the superfamily of voltage-gated K(+) channel. In mammals, the expression of Eag channels is neuron-specific but their neurophysiological role remains obscure. We have applied the yeast two-hybrid screening system to identify rat Eag1 (rEag...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401112/ https://www.ncbi.nlm.nih.gov/pubmed/22911758 http://dx.doi.org/10.1371/journal.pone.0041203 |
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author | Hsu, Po-Hao Miaw, Shi-Chuen Chuang, Chau-Ching Chang, Pei-Yu Fu, Ssu-Ju Jow, Guey-Mei Chiu, Mei-Miao Jeng, Chung-Jiuan |
author_facet | Hsu, Po-Hao Miaw, Shi-Chuen Chuang, Chau-Ching Chang, Pei-Yu Fu, Ssu-Ju Jow, Guey-Mei Chiu, Mei-Miao Jeng, Chung-Jiuan |
author_sort | Hsu, Po-Hao |
collection | PubMed |
description | The ether-à-go-go (Eag) potassium (K(+)) channel belongs to the superfamily of voltage-gated K(+) channel. In mammals, the expression of Eag channels is neuron-specific but their neurophysiological role remains obscure. We have applied the yeast two-hybrid screening system to identify rat Eag1 (rEag1)-interacting proteins from a rat brain cDNA library. One of the clones we identified was 14-3-3θ, which belongs to a family of small acidic protein abundantly expressed in the brain. Data from in vitro yeast two-hybrid and GST pull-down assays suggested that the direct association with 14-3-3θ was mediated by both the N- and the C-termini of rEag1. Co-precipitation of the two proteins was confirmed in both heterologous HEK293T cells and native hippocampal neurons. Electrophysiological studies showed that over-expression of 14-3-3θ led to a sizable suppression of rEag1 K(+) currents with no apparent alteration of the steady-state voltage dependence and gating kinetics. Furthermore, co-expression with 14-3-3θ failed to affect the total protein level, membrane trafficking, and single channel conductance of rEag1, implying that 14-3-3θ binding may render a fraction of the channel locked in a non-conducting state. Together these data suggest that 14-3-3θ is a binding partner of rEag1 and may modulate the functional expression of the K(+) channel in neurons. |
format | Online Article Text |
id | pubmed-3401112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34011122012-07-30 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels Hsu, Po-Hao Miaw, Shi-Chuen Chuang, Chau-Ching Chang, Pei-Yu Fu, Ssu-Ju Jow, Guey-Mei Chiu, Mei-Miao Jeng, Chung-Jiuan PLoS One Research Article The ether-à-go-go (Eag) potassium (K(+)) channel belongs to the superfamily of voltage-gated K(+) channel. In mammals, the expression of Eag channels is neuron-specific but their neurophysiological role remains obscure. We have applied the yeast two-hybrid screening system to identify rat Eag1 (rEag1)-interacting proteins from a rat brain cDNA library. One of the clones we identified was 14-3-3θ, which belongs to a family of small acidic protein abundantly expressed in the brain. Data from in vitro yeast two-hybrid and GST pull-down assays suggested that the direct association with 14-3-3θ was mediated by both the N- and the C-termini of rEag1. Co-precipitation of the two proteins was confirmed in both heterologous HEK293T cells and native hippocampal neurons. Electrophysiological studies showed that over-expression of 14-3-3θ led to a sizable suppression of rEag1 K(+) currents with no apparent alteration of the steady-state voltage dependence and gating kinetics. Furthermore, co-expression with 14-3-3θ failed to affect the total protein level, membrane trafficking, and single channel conductance of rEag1, implying that 14-3-3θ binding may render a fraction of the channel locked in a non-conducting state. Together these data suggest that 14-3-3θ is a binding partner of rEag1 and may modulate the functional expression of the K(+) channel in neurons. Public Library of Science 2012-07-20 /pmc/articles/PMC3401112/ /pubmed/22911758 http://dx.doi.org/10.1371/journal.pone.0041203 Text en Hsu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hsu, Po-Hao Miaw, Shi-Chuen Chuang, Chau-Ching Chang, Pei-Yu Fu, Ssu-Ju Jow, Guey-Mei Chiu, Mei-Miao Jeng, Chung-Jiuan 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title | 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title_full | 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title_fullStr | 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title_full_unstemmed | 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title_short | 14-3-3θ is a Binding Partner of Rat Eag1 Potassium Channels |
title_sort | 14-3-3θ is a binding partner of rat eag1 potassium channels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401112/ https://www.ncbi.nlm.nih.gov/pubmed/22911758 http://dx.doi.org/10.1371/journal.pone.0041203 |
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