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Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport

Connexin 43 (Cx43, encoded by GJA1) is a cell-cell communication gap junction protein expressed in all organ systems. It was recently found that GJA1 mRNA undergoes alternative translation to generate N-terminal truncated isoforms, of which GJA1-20k is the most abundant. Here we report a surprising...

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Autores principales: Fu, Ying, Zhang, Shan-Shan, Xiao, Shaohua, Basheer, Wassim A., Baum, Rachel, Epifantseva, Irina, Hong, TingTing, Shaw, Robin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682029/
https://www.ncbi.nlm.nih.gov/pubmed/29163229
http://dx.doi.org/10.3389/fphys.2017.00905
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author Fu, Ying
Zhang, Shan-Shan
Xiao, Shaohua
Basheer, Wassim A.
Baum, Rachel
Epifantseva, Irina
Hong, TingTing
Shaw, Robin M.
author_facet Fu, Ying
Zhang, Shan-Shan
Xiao, Shaohua
Basheer, Wassim A.
Baum, Rachel
Epifantseva, Irina
Hong, TingTing
Shaw, Robin M.
author_sort Fu, Ying
collection PubMed
description Connexin 43 (Cx43, encoded by GJA1) is a cell-cell communication gap junction protein expressed in all organ systems. It was recently found that GJA1 mRNA undergoes alternative translation to generate N-terminal truncated isoforms, of which GJA1-20k is the most abundant. Here we report a surprising finding that, unlike full length GJA1-43k, GJA1-20k has a strong tropism for mitochondria. Exploring function, we found that GJA1-20k appears to be an organelle chaperone and that overexpression of GJA1-20k is sufficient to rescue mitochondrial localization to the cell periphery upon exposure to hydrogen peroxide, which effectively limits the network fragmentation that occurs with oxidative stress. By high-resolution fluorescent imaging and electron microscopy, we determined that GJA1-20k is enriched at the interface between mitochondria and microtubules, appearing to load organelles for transport. Mutagenesis experiments revealed that although the microtubule-binding domain (MTBD) in GJA1-20k is not necessary for protein localization to mitochondria, the MTBD is essential for GJA1-20k to facilitate mitochondrial transport and maintain mitochondrial localization at the periphery. These results reveal an unexpected role for the alternatively translated isoform of the Cx43 gap junction protein, GJA1-20k, which is to facilitate microtubule-based mitochondrial transport and to maintain mitochondrial network integrity during cellular stress.
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spelling pubmed-56820292017-11-21 Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport Fu, Ying Zhang, Shan-Shan Xiao, Shaohua Basheer, Wassim A. Baum, Rachel Epifantseva, Irina Hong, TingTing Shaw, Robin M. Front Physiol Physiology Connexin 43 (Cx43, encoded by GJA1) is a cell-cell communication gap junction protein expressed in all organ systems. It was recently found that GJA1 mRNA undergoes alternative translation to generate N-terminal truncated isoforms, of which GJA1-20k is the most abundant. Here we report a surprising finding that, unlike full length GJA1-43k, GJA1-20k has a strong tropism for mitochondria. Exploring function, we found that GJA1-20k appears to be an organelle chaperone and that overexpression of GJA1-20k is sufficient to rescue mitochondrial localization to the cell periphery upon exposure to hydrogen peroxide, which effectively limits the network fragmentation that occurs with oxidative stress. By high-resolution fluorescent imaging and electron microscopy, we determined that GJA1-20k is enriched at the interface between mitochondria and microtubules, appearing to load organelles for transport. Mutagenesis experiments revealed that although the microtubule-binding domain (MTBD) in GJA1-20k is not necessary for protein localization to mitochondria, the MTBD is essential for GJA1-20k to facilitate mitochondrial transport and maintain mitochondrial localization at the periphery. These results reveal an unexpected role for the alternatively translated isoform of the Cx43 gap junction protein, GJA1-20k, which is to facilitate microtubule-based mitochondrial transport and to maintain mitochondrial network integrity during cellular stress. Frontiers Media S.A. 2017-11-07 /pmc/articles/PMC5682029/ /pubmed/29163229 http://dx.doi.org/10.3389/fphys.2017.00905 Text en Copyright © 2017 Fu, Zhang, Xiao, Basheer, Baum, Epifantseva, Hong and Shaw. http://creativecommons.org/licenses/by/4.0/ 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 Physiology
Fu, Ying
Zhang, Shan-Shan
Xiao, Shaohua
Basheer, Wassim A.
Baum, Rachel
Epifantseva, Irina
Hong, TingTing
Shaw, Robin M.
Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title_full Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title_fullStr Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title_full_unstemmed Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title_short Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport
title_sort cx43 isoform gja1-20k promotes microtubule dependent mitochondrial transport
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682029/
https://www.ncbi.nlm.nih.gov/pubmed/29163229
http://dx.doi.org/10.3389/fphys.2017.00905
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