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Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin
RhoA, a small GTPase, regulates epithelial integrity and morphogenesis by controlling filamentous actin assembly and actomyosin contractility. Another important cytoskeletal regulator, Moesin (Moe), an ezrin, radixin, and moesin (ERM) protein, has the ability to bind to and organize cortical F-actin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639053/ https://www.ncbi.nlm.nih.gov/pubmed/23468526 http://dx.doi.org/10.1091/mbc.E12-11-0800 |
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author | Neisch, Amanda L. Formstecher, Etienne Fehon, Richard G. |
author_facet | Neisch, Amanda L. Formstecher, Etienne Fehon, Richard G. |
author_sort | Neisch, Amanda L. |
collection | PubMed |
description | RhoA, a small GTPase, regulates epithelial integrity and morphogenesis by controlling filamentous actin assembly and actomyosin contractility. Another important cytoskeletal regulator, Moesin (Moe), an ezrin, radixin, and moesin (ERM) protein, has the ability to bind to and organize cortical F-actin, as well as the ability to regulate RhoA activity. ERM proteins have previously been shown to interact with both RhoGEF (guanine nucleotide exchange factors) and RhoGAP (GTPase activating proteins), proteins that control the activation state of RhoA, but the functions of these interactions remain unclear. We demonstrate that Moe interacts with an unusual RhoGAP, Conundrum (Conu), and recruits it to the cell cortex to negatively regulate RhoA activity. In addition, we show that cortically localized Conu can promote cell proliferation and that this function requires RhoGAP activity. Surprisingly, Conu's ability to promote growth also appears dependent on increased Rac activity. Our results reveal a molecular mechanism by which ERM proteins control RhoA activity and suggest a novel linkage between the small GTPases RhoA and Rac in growth control. |
format | Online Article Text |
id | pubmed-3639053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-36390532013-07-16 Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin Neisch, Amanda L. Formstecher, Etienne Fehon, Richard G. Mol Biol Cell Articles RhoA, a small GTPase, regulates epithelial integrity and morphogenesis by controlling filamentous actin assembly and actomyosin contractility. Another important cytoskeletal regulator, Moesin (Moe), an ezrin, radixin, and moesin (ERM) protein, has the ability to bind to and organize cortical F-actin, as well as the ability to regulate RhoA activity. ERM proteins have previously been shown to interact with both RhoGEF (guanine nucleotide exchange factors) and RhoGAP (GTPase activating proteins), proteins that control the activation state of RhoA, but the functions of these interactions remain unclear. We demonstrate that Moe interacts with an unusual RhoGAP, Conundrum (Conu), and recruits it to the cell cortex to negatively regulate RhoA activity. In addition, we show that cortically localized Conu can promote cell proliferation and that this function requires RhoGAP activity. Surprisingly, Conu's ability to promote growth also appears dependent on increased Rac activity. Our results reveal a molecular mechanism by which ERM proteins control RhoA activity and suggest a novel linkage between the small GTPases RhoA and Rac in growth control. The American Society for Cell Biology 2013-05-01 /pmc/articles/PMC3639053/ /pubmed/23468526 http://dx.doi.org/10.1091/mbc.E12-11-0800 Text en © 2013 Neisch et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell BD; are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Neisch, Amanda L. Formstecher, Etienne Fehon, Richard G. Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title | Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title_full | Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title_fullStr | Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title_full_unstemmed | Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title_short | Conundrum, an ARHGAP18 orthologue, regulates RhoA and proliferation through interactions with Moesin |
title_sort | conundrum, an arhgap18 orthologue, regulates rhoa and proliferation through interactions with moesin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639053/ https://www.ncbi.nlm.nih.gov/pubmed/23468526 http://dx.doi.org/10.1091/mbc.E12-11-0800 |
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