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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...

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Autores principales: Hsu, Po-Hao, Miaw, Shi-Chuen, Chuang, Chau-Ching, Chang, Pei-Yu, Fu, Ssu-Ju, Jow, Guey-Mei, Chiu, Mei-Miao, Jeng, Chung-Jiuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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