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Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration

Drosophila RhoGAP18B was identified as a negative regulator of small GTPase in the behavioral response to ethanol. However, the effect of RhoGAP18B on cell migration is unknown. Here, we report that RhoGAP18B regulates the migration of border cells in Drosophila ovary. The RhoGAP18B gene produces fo...

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Detalles Bibliográficos
Autores principales: Lei, Fengyun, Xu, Xiaoqing, Huang, Jianhua, Su, Dan, Wan, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858088/
https://www.ncbi.nlm.nih.gov/pubmed/36662713
http://dx.doi.org/10.1371/journal.pone.0280652
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author Lei, Fengyun
Xu, Xiaoqing
Huang, Jianhua
Su, Dan
Wan, Ping
author_facet Lei, Fengyun
Xu, Xiaoqing
Huang, Jianhua
Su, Dan
Wan, Ping
author_sort Lei, Fengyun
collection PubMed
description Drosophila RhoGAP18B was identified as a negative regulator of small GTPase in the behavioral response to ethanol. However, the effect of RhoGAP18B on cell migration is unknown. Here, we report that RhoGAP18B regulates the migration of border cells in Drosophila ovary. The RhoGAP18B gene produces four transcripts and encodes three translation isoforms. We use different RNAi lines to knockdown each RhoGAP18B isoform, and find that knockdown of RhoGAP18B-PA, but not PC or PD isoform, blocks border cell migration. Knockdown of RhoGAP18B-PA disrupts the asymmetric distribution of F-actin in border cell cluster and increases F-actin level. Furthermore, RhoGAP18B-PA may act on Rac to regulate F-actin organization. Our data indicate that RhoGAP18B shows isoform-specific regulation of border cell migration.
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spelling pubmed-98580882023-01-21 Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration Lei, Fengyun Xu, Xiaoqing Huang, Jianhua Su, Dan Wan, Ping PLoS One Research Article Drosophila RhoGAP18B was identified as a negative regulator of small GTPase in the behavioral response to ethanol. However, the effect of RhoGAP18B on cell migration is unknown. Here, we report that RhoGAP18B regulates the migration of border cells in Drosophila ovary. The RhoGAP18B gene produces four transcripts and encodes three translation isoforms. We use different RNAi lines to knockdown each RhoGAP18B isoform, and find that knockdown of RhoGAP18B-PA, but not PC or PD isoform, blocks border cell migration. Knockdown of RhoGAP18B-PA disrupts the asymmetric distribution of F-actin in border cell cluster and increases F-actin level. Furthermore, RhoGAP18B-PA may act on Rac to regulate F-actin organization. Our data indicate that RhoGAP18B shows isoform-specific regulation of border cell migration. Public Library of Science 2023-01-20 /pmc/articles/PMC9858088/ /pubmed/36662713 http://dx.doi.org/10.1371/journal.pone.0280652 Text en © 2023 Lei et al https://creativecommons.org/licenses/by/4.0/This 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 the original author and source are credited.
spellingShingle Research Article
Lei, Fengyun
Xu, Xiaoqing
Huang, Jianhua
Su, Dan
Wan, Ping
Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title_full Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title_fullStr Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title_full_unstemmed Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title_short Drosophila RhoGAP18B regulates actin cytoskeleton during border cell migration
title_sort drosophila rhogap18b regulates actin cytoskeleton during border cell migration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858088/
https://www.ncbi.nlm.nih.gov/pubmed/36662713
http://dx.doi.org/10.1371/journal.pone.0280652
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