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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...

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Autores principales: Walck-Shannon, Elise, Lucas, Bethany, Chin-Sang, Ian, Reiner, David, Kumfer, Kraig, Cochran, Hunter, Bothfeld, William, Hardin, Jeff
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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.
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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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