Cargando…
RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia
CDC-42 regulation of non-muscle myosin/NMY-2 is required for polarity maintenance in the one-cell embryo of Caenorhabditis elegans. CDC-42 and NMY-2 regulate polarity throughout embryogenesis, but their contribution to later events of morphogenesis are less understood. We have shown that epidermal e...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710025/ https://www.ncbi.nlm.nih.gov/pubmed/33243762 http://dx.doi.org/10.1242/bio.056911 |
_version_ | 1783617862207799296 |
---|---|
author | Raduwan, Hamidah Sasidharan, Shashikala Burgos, Luigy Cordova Wallace, Andre G. Soto, Martha C. |
author_facet | Raduwan, Hamidah Sasidharan, Shashikala Burgos, Luigy Cordova Wallace, Andre G. Soto, Martha C. |
author_sort | Raduwan, Hamidah |
collection | PubMed |
description | CDC-42 regulation of non-muscle myosin/NMY-2 is required for polarity maintenance in the one-cell embryo of Caenorhabditis elegans. CDC-42 and NMY-2 regulate polarity throughout embryogenesis, but their contribution to later events of morphogenesis are less understood. We have shown that epidermal enclosure requires the GTPase CED-10/Rac1 and WAVE/Scar complex, its effector, to promote protrusions that drive enclosure through the branch actin regulator Arp2/3. Our analysis here of RGA-8, a homolog of SH3BP1/Rich1/ARHGAP17/Nadrin, with BAR and RhoGAP motifs, suggests it regulates CDC-42, so that actin and myosin/NMY-2 promote ventral enclosure during embryonic morphogenesis. Genetic and molecular data suggest RGA-8 regulates CDC-42, and phenocopies the CDC-42 pathway regulators WASP-1/WSP-1 and the F-BAR proteins TOCA-1 and TOCA-2. Live imaging shows RGA-8 and WSP-1 enrich myosin and regulate F-actin in migrating epidermal cells during ventral enclosure. Loss of RGA-8 alters membrane recruitment of active CDC-42. We propose TOCA proteins and RGA-8 use BAR domains to localize and regenerate CDC-42 activity, thus regulating F-actin levels, through the branched actin regulator WSP-1, and myosin enrichment. RhoGAP RGA-8 thus polarizes epithelia, to promote cell migrations and cell shape changes of embryonic morphogenesis. |
format | Online Article Text |
id | pubmed-7710025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-77100252020-12-03 RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia Raduwan, Hamidah Sasidharan, Shashikala Burgos, Luigy Cordova Wallace, Andre G. Soto, Martha C. Biol Open Research Article CDC-42 regulation of non-muscle myosin/NMY-2 is required for polarity maintenance in the one-cell embryo of Caenorhabditis elegans. CDC-42 and NMY-2 regulate polarity throughout embryogenesis, but their contribution to later events of morphogenesis are less understood. We have shown that epidermal enclosure requires the GTPase CED-10/Rac1 and WAVE/Scar complex, its effector, to promote protrusions that drive enclosure through the branch actin regulator Arp2/3. Our analysis here of RGA-8, a homolog of SH3BP1/Rich1/ARHGAP17/Nadrin, with BAR and RhoGAP motifs, suggests it regulates CDC-42, so that actin and myosin/NMY-2 promote ventral enclosure during embryonic morphogenesis. Genetic and molecular data suggest RGA-8 regulates CDC-42, and phenocopies the CDC-42 pathway regulators WASP-1/WSP-1 and the F-BAR proteins TOCA-1 and TOCA-2. Live imaging shows RGA-8 and WSP-1 enrich myosin and regulate F-actin in migrating epidermal cells during ventral enclosure. Loss of RGA-8 alters membrane recruitment of active CDC-42. We propose TOCA proteins and RGA-8 use BAR domains to localize and regenerate CDC-42 activity, thus regulating F-actin levels, through the branched actin regulator WSP-1, and myosin enrichment. RhoGAP RGA-8 thus polarizes epithelia, to promote cell migrations and cell shape changes of embryonic morphogenesis. The Company of Biologists Ltd 2020-11-26 /pmc/articles/PMC7710025/ /pubmed/33243762 http://dx.doi.org/10.1242/bio.056911 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Raduwan, Hamidah Sasidharan, Shashikala Burgos, Luigy Cordova Wallace, Andre G. Soto, Martha C. RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title | RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title_full | RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title_fullStr | RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title_full_unstemmed | RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title_short | RhoGAP RGA-8 supports morphogenesis in C. elegans by polarizing epithelia |
title_sort | rhogap rga-8 supports morphogenesis in c. elegans by polarizing epithelia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710025/ https://www.ncbi.nlm.nih.gov/pubmed/33243762 http://dx.doi.org/10.1242/bio.056911 |
work_keys_str_mv | AT raduwanhamidah rhogaprga8supportsmorphogenesisincelegansbypolarizingepithelia AT sasidharanshashikala rhogaprga8supportsmorphogenesisincelegansbypolarizingepithelia AT burgosluigycordova rhogaprga8supportsmorphogenesisincelegansbypolarizingepithelia AT wallaceandreg rhogaprga8supportsmorphogenesisincelegansbypolarizingepithelia AT sotomarthac rhogaprga8supportsmorphogenesisincelegansbypolarizingepithelia |