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Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle
C. elegans body-wall muscle cells are electrically coupled through gap junctions. Previous studies suggest that UNC-9 is an important, but not the only, innexin mediating the electrical coupling. Here we analyzed junctional current (I (j)) for mutants of additional innexins to identify the remaining...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793928/ https://www.ncbi.nlm.nih.gov/pubmed/24130800 http://dx.doi.org/10.1371/journal.pone.0076877 |
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author | Liu, Ping Chen, Bojun Altun, Zeynep F. Gross, Maegan J. Shan, Alan Schuman, Benjamin Hall, David H. Wang, Zhao-Wen |
author_facet | Liu, Ping Chen, Bojun Altun, Zeynep F. Gross, Maegan J. Shan, Alan Schuman, Benjamin Hall, David H. Wang, Zhao-Wen |
author_sort | Liu, Ping |
collection | PubMed |
description | C. elegans body-wall muscle cells are electrically coupled through gap junctions. Previous studies suggest that UNC-9 is an important, but not the only, innexin mediating the electrical coupling. Here we analyzed junctional current (I (j)) for mutants of additional innexins to identify the remaining innexin(s) important to the coupling. The results suggest that a total of six innexins contribute to the coupling, including UNC-9, INX-1, INX-10, INX-11, INX-16, and INX-18. The I (j) deficiency in each mutant was rescued completely by expressing the corresponding wild-type innexin specifically in muscle, suggesting that the innexins function cell-autonomously. Comparisons of I (j) between various single, double, and triple mutants suggest that the six innexins probably form two distinct populations of gap junctions with one population consisting of UNC-9 and INX-18 and the other consisting of the remaining four innexins. Consistent with their roles in muscle electrical coupling, five of the six innexins showed punctate localization at muscle intercellular junctions when expressed as GFP- or epitope-tagged proteins, and muscle expression was detected for four of them when assessed by expressing GFP under the control of innexin promoters. The results may serve as a solid foundation for further explorations of structural and functional properties of gap junctions in C. elegans body-wall muscle. |
format | Online Article Text |
id | pubmed-3793928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37939282013-10-15 Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle Liu, Ping Chen, Bojun Altun, Zeynep F. Gross, Maegan J. Shan, Alan Schuman, Benjamin Hall, David H. Wang, Zhao-Wen PLoS One Research Article C. elegans body-wall muscle cells are electrically coupled through gap junctions. Previous studies suggest that UNC-9 is an important, but not the only, innexin mediating the electrical coupling. Here we analyzed junctional current (I (j)) for mutants of additional innexins to identify the remaining innexin(s) important to the coupling. The results suggest that a total of six innexins contribute to the coupling, including UNC-9, INX-1, INX-10, INX-11, INX-16, and INX-18. The I (j) deficiency in each mutant was rescued completely by expressing the corresponding wild-type innexin specifically in muscle, suggesting that the innexins function cell-autonomously. Comparisons of I (j) between various single, double, and triple mutants suggest that the six innexins probably form two distinct populations of gap junctions with one population consisting of UNC-9 and INX-18 and the other consisting of the remaining four innexins. Consistent with their roles in muscle electrical coupling, five of the six innexins showed punctate localization at muscle intercellular junctions when expressed as GFP- or epitope-tagged proteins, and muscle expression was detected for four of them when assessed by expressing GFP under the control of innexin promoters. The results may serve as a solid foundation for further explorations of structural and functional properties of gap junctions in C. elegans body-wall muscle. Public Library of Science 2013-10-09 /pmc/articles/PMC3793928/ /pubmed/24130800 http://dx.doi.org/10.1371/journal.pone.0076877 Text en © 2013 Liu 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 Liu, Ping Chen, Bojun Altun, Zeynep F. Gross, Maegan J. Shan, Alan Schuman, Benjamin Hall, David H. Wang, Zhao-Wen Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title | Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title_full | Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title_fullStr | Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title_full_unstemmed | Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title_short | Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle |
title_sort | six innexins contribute to electrical coupling of c. elegans body-wall muscle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793928/ https://www.ncbi.nlm.nih.gov/pubmed/24130800 http://dx.doi.org/10.1371/journal.pone.0076877 |
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