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Role of ARHGEF3 as a GEF and mTORC2 Regulator
Guanine nucleotide exchange factors (GEFs) activate GTPases by stimulating the release of guanosine diphosphate to permit the binding of guanosine triphosphate. ARHGEF3 or XPLN (exchange factor found in platelets, leukemic, and neuronal tissues) is a selective guanine nucleotide exchange factor for...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841341/ https://www.ncbi.nlm.nih.gov/pubmed/35174167 http://dx.doi.org/10.3389/fcell.2021.806258 |
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author | Khaliq, Sana Abdul Umair, Zobia Yoon, Mee-Sup |
author_facet | Khaliq, Sana Abdul Umair, Zobia Yoon, Mee-Sup |
author_sort | Khaliq, Sana Abdul |
collection | PubMed |
description | Guanine nucleotide exchange factors (GEFs) activate GTPases by stimulating the release of guanosine diphosphate to permit the binding of guanosine triphosphate. ARHGEF3 or XPLN (exchange factor found in platelets, leukemic, and neuronal tissues) is a selective guanine nucleotide exchange factor for Rho GTPases (RhoGEFs) that activates RhoA and RhoB but not RhoC, RhoG, Rac1, or Cdc42. ARHGEF3 contains the diffuse B-cell lymphoma homology and pleckstrin homology domains but lacks similarity with other known functional domains. ARHGEF3 also binds the mammalian target of rapamycin complex 2 (mTORC2) and subsequently inhibits mTORC2 and Akt. In vivo investigation has also indicated the communication between ARHGEF3 and autophagy-related muscle pathologies. Moreover, studies on genetic variation in ARHGEF3 and genome-wide association studies have predicted exciting novel roles of ARHGEF3 in controlling bone mineral density, platelet formation and differentiation, and Hirschsprung disease. In conclusion, we hypothesized that additional biochemical and functional studies are required to elucidate the detailed mechanism of ARHGEF3-related pathologies and therapeutics. |
format | Online Article Text |
id | pubmed-8841341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88413412022-02-15 Role of ARHGEF3 as a GEF and mTORC2 Regulator Khaliq, Sana Abdul Umair, Zobia Yoon, Mee-Sup Front Cell Dev Biol Cell and Developmental Biology Guanine nucleotide exchange factors (GEFs) activate GTPases by stimulating the release of guanosine diphosphate to permit the binding of guanosine triphosphate. ARHGEF3 or XPLN (exchange factor found in platelets, leukemic, and neuronal tissues) is a selective guanine nucleotide exchange factor for Rho GTPases (RhoGEFs) that activates RhoA and RhoB but not RhoC, RhoG, Rac1, or Cdc42. ARHGEF3 contains the diffuse B-cell lymphoma homology and pleckstrin homology domains but lacks similarity with other known functional domains. ARHGEF3 also binds the mammalian target of rapamycin complex 2 (mTORC2) and subsequently inhibits mTORC2 and Akt. In vivo investigation has also indicated the communication between ARHGEF3 and autophagy-related muscle pathologies. Moreover, studies on genetic variation in ARHGEF3 and genome-wide association studies have predicted exciting novel roles of ARHGEF3 in controlling bone mineral density, platelet formation and differentiation, and Hirschsprung disease. In conclusion, we hypothesized that additional biochemical and functional studies are required to elucidate the detailed mechanism of ARHGEF3-related pathologies and therapeutics. Frontiers Media S.A. 2022-01-31 /pmc/articles/PMC8841341/ /pubmed/35174167 http://dx.doi.org/10.3389/fcell.2021.806258 Text en Copyright © 2022 Khaliq, Umair and Yoon. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Khaliq, Sana Abdul Umair, Zobia Yoon, Mee-Sup Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title | Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title_full | Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title_fullStr | Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title_full_unstemmed | Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title_short | Role of ARHGEF3 as a GEF and mTORC2 Regulator |
title_sort | role of arhgef3 as a gef and mtorc2 regulator |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841341/ https://www.ncbi.nlm.nih.gov/pubmed/35174167 http://dx.doi.org/10.3389/fcell.2021.806258 |
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