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Managing the complexity of communication: regulation of gap junctions by post-translational modification

Gap junctions are comprised of connexins that form cell-to-cell channels which couple neighboring cells to accommodate the exchange of information. The need for communication does, however, change over time and therefore must be tightly controlled. Although the regulation of connexin protein express...

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Autores principales: Axelsen, Lene N., Calloe, Kirstine, Holstein-Rathlou, Niels-Henrik, Nielsen, Morten S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804956/
https://www.ncbi.nlm.nih.gov/pubmed/24155720
http://dx.doi.org/10.3389/fphar.2013.00130
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author Axelsen, Lene N.
Calloe, Kirstine
Holstein-Rathlou, Niels-Henrik
Nielsen, Morten S.
author_facet Axelsen, Lene N.
Calloe, Kirstine
Holstein-Rathlou, Niels-Henrik
Nielsen, Morten S.
author_sort Axelsen, Lene N.
collection PubMed
description Gap junctions are comprised of connexins that form cell-to-cell channels which couple neighboring cells to accommodate the exchange of information. The need for communication does, however, change over time and therefore must be tightly controlled. Although the regulation of connexin protein expression by transcription and translation is of great importance, the trafficking, channel activity and degradation are also under tight control. The function of connexins can be regulated by several post translational modifications, which affect numerous parameters; including number of channels, open probability, single channel conductance or selectivity. The most extensively investigated post translational modifications are phosphorylations, which have been documented in all mammalian connexins. Besides phosphorylations, some connexins are known to be ubiquitinated, SUMOylated, nitrosylated, hydroxylated, acetylated, methylated, and γ-carboxyglutamated. The aim of the present review is to summarize our current knowledge of post translational regulation of the connexin family of proteins.
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spelling pubmed-38049562013-10-23 Managing the complexity of communication: regulation of gap junctions by post-translational modification Axelsen, Lene N. Calloe, Kirstine Holstein-Rathlou, Niels-Henrik Nielsen, Morten S. Front Pharmacol Pharmacology Gap junctions are comprised of connexins that form cell-to-cell channels which couple neighboring cells to accommodate the exchange of information. The need for communication does, however, change over time and therefore must be tightly controlled. Although the regulation of connexin protein expression by transcription and translation is of great importance, the trafficking, channel activity and degradation are also under tight control. The function of connexins can be regulated by several post translational modifications, which affect numerous parameters; including number of channels, open probability, single channel conductance or selectivity. The most extensively investigated post translational modifications are phosphorylations, which have been documented in all mammalian connexins. Besides phosphorylations, some connexins are known to be ubiquitinated, SUMOylated, nitrosylated, hydroxylated, acetylated, methylated, and γ-carboxyglutamated. The aim of the present review is to summarize our current knowledge of post translational regulation of the connexin family of proteins. Frontiers Media S.A. 2013-10-22 /pmc/articles/PMC3804956/ /pubmed/24155720 http://dx.doi.org/10.3389/fphar.2013.00130 Text en Copyright © Axelsen, Calloe, Holstein-Rathlou and Nielsen. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Axelsen, Lene N.
Calloe, Kirstine
Holstein-Rathlou, Niels-Henrik
Nielsen, Morten S.
Managing the complexity of communication: regulation of gap junctions by post-translational modification
title Managing the complexity of communication: regulation of gap junctions by post-translational modification
title_full Managing the complexity of communication: regulation of gap junctions by post-translational modification
title_fullStr Managing the complexity of communication: regulation of gap junctions by post-translational modification
title_full_unstemmed Managing the complexity of communication: regulation of gap junctions by post-translational modification
title_short Managing the complexity of communication: regulation of gap junctions by post-translational modification
title_sort managing the complexity of communication: regulation of gap junctions by post-translational modification
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804956/
https://www.ncbi.nlm.nih.gov/pubmed/24155720
http://dx.doi.org/10.3389/fphar.2013.00130
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