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CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis
Cell intercalation is a highly directed cell rearrangement that is essential for animal morphogenesis. As such, intercalation requires orchestration of cell polarity across the plane of the tissue. CDC-42 is a Rho family GTPase with key functions in cell polarity, yet its role during epithelial inte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127194/ https://www.ncbi.nlm.nih.gov/pubmed/27861585 http://dx.doi.org/10.1371/journal.pgen.1006415 |
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author | Walck-Shannon, Elise Lucas, Bethany Chin-Sang, Ian Reiner, David Kumfer, Kraig Cochran, Hunter Bothfeld, William Hardin, Jeff |
author_facet | Walck-Shannon, Elise Lucas, Bethany Chin-Sang, Ian Reiner, David Kumfer, Kraig Cochran, Hunter Bothfeld, William Hardin, Jeff |
author_sort | Walck-Shannon, Elise |
collection | PubMed |
description | Cell intercalation is a highly directed cell rearrangement that is essential for animal morphogenesis. As such, intercalation requires orchestration of cell polarity across the plane of the tissue. CDC-42 is a Rho family GTPase with key functions in cell polarity, yet its role during epithelial intercalation has not been established because its roles early in embryogenesis have historically made it difficult to study. To circumvent these early requirements, in this paper we use tissue-specific and conditional loss-of-function approaches to identify a role for CDC-42 during intercalation of the Caenorhabditis elegans dorsal embryonic epidermis. CDC-42 activity is enriched in the medial tips of intercalating cells, which extend as cells migrate past one another. Moreover, CDC-42 is involved in both the efficient formation and orientation of cell tips during cell rearrangement. Using conditional loss-of-function we also show that the PAR complex functions in tip formation and orientation. Additionally, we find that the sole C. elegans Eph receptor, VAB-1, functions during this process in an Ephrin-independent manner. Using epistasis analysis, we find that vab-1 lies in the same genetic pathway as cdc-42 and is responsible for polarizing CDC-42 activity to the medial tip. Together, these data establish a previously uncharacterized role for polarized CDC-42, in conjunction with PAR-6, PAR-3 and an Eph receptor, during epithelial intercalation. |
format | Online Article Text |
id | pubmed-5127194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51271942016-12-15 CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis Walck-Shannon, Elise Lucas, Bethany Chin-Sang, Ian Reiner, David Kumfer, Kraig Cochran, Hunter Bothfeld, William Hardin, Jeff PLoS Genet Research Article Cell intercalation is a highly directed cell rearrangement that is essential for animal morphogenesis. As such, intercalation requires orchestration of cell polarity across the plane of the tissue. CDC-42 is a Rho family GTPase with key functions in cell polarity, yet its role during epithelial intercalation has not been established because its roles early in embryogenesis have historically made it difficult to study. To circumvent these early requirements, in this paper we use tissue-specific and conditional loss-of-function approaches to identify a role for CDC-42 during intercalation of the Caenorhabditis elegans dorsal embryonic epidermis. CDC-42 activity is enriched in the medial tips of intercalating cells, which extend as cells migrate past one another. Moreover, CDC-42 is involved in both the efficient formation and orientation of cell tips during cell rearrangement. Using conditional loss-of-function we also show that the PAR complex functions in tip formation and orientation. Additionally, we find that the sole C. elegans Eph receptor, VAB-1, functions during this process in an Ephrin-independent manner. Using epistasis analysis, we find that vab-1 lies in the same genetic pathway as cdc-42 and is responsible for polarizing CDC-42 activity to the medial tip. Together, these data establish a previously uncharacterized role for polarized CDC-42, in conjunction with PAR-6, PAR-3 and an Eph receptor, during epithelial intercalation. Public Library of Science 2016-11-18 /pmc/articles/PMC5127194/ /pubmed/27861585 http://dx.doi.org/10.1371/journal.pgen.1006415 Text en © 2016 Walck-Shannon 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Walck-Shannon, Elise Lucas, Bethany Chin-Sang, Ian Reiner, David Kumfer, Kraig Cochran, Hunter Bothfeld, William Hardin, Jeff CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title_full | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title_fullStr | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title_full_unstemmed | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title_short | CDC-42 Orients Cell Migration during Epithelial Intercalation in the Caenorhabditis elegans Epidermis |
title_sort | cdc-42 orients cell migration during epithelial intercalation in the caenorhabditis elegans epidermis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127194/ https://www.ncbi.nlm.nih.gov/pubmed/27861585 http://dx.doi.org/10.1371/journal.pgen.1006415 |
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