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The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer

Rho family small guanosine triphosphatases (GTPases) are important regulators of the cytoskeleton, and are critical in many aspects of cellular and developmental biology, as well as in pathological processes such as intellectual disability and cancer. Of the three members of the family, Rac3 has a m...

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Detalles Bibliográficos
Autor principal: de Curtis, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770886/
https://www.ncbi.nlm.nih.gov/pubmed/31514269
http://dx.doi.org/10.3390/cells8091063
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description Rho family small guanosine triphosphatases (GTPases) are important regulators of the cytoskeleton, and are critical in many aspects of cellular and developmental biology, as well as in pathological processes such as intellectual disability and cancer. Of the three members of the family, Rac3 has a more restricted expression in normal tissues compared to the ubiquitous member of the family, Rac1. The Rac3 polypeptide is highly similar to Rac1, and orthologues of the gene for Rac3 have been found only in vertebrates, indicating the late appearance of this gene during evolution. Increasing evidence over the past few years indicates that Rac3 plays an important role in neuronal development and in tumor progression, with specificities that distinguish the functions of Rac3 from the established functions of Rac1 in these processes. Here, results highlighting the importance of Rac3 in distinct aspects of neuronal development and tumor cell biology are presented, in support of the non-redundant role of different members of the two Rac GTPases in physiological and pathological processes.
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spelling pubmed-67708862019-10-30 The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer de Curtis, Ivan Cells Review Rho family small guanosine triphosphatases (GTPases) are important regulators of the cytoskeleton, and are critical in many aspects of cellular and developmental biology, as well as in pathological processes such as intellectual disability and cancer. Of the three members of the family, Rac3 has a more restricted expression in normal tissues compared to the ubiquitous member of the family, Rac1. The Rac3 polypeptide is highly similar to Rac1, and orthologues of the gene for Rac3 have been found only in vertebrates, indicating the late appearance of this gene during evolution. Increasing evidence over the past few years indicates that Rac3 plays an important role in neuronal development and in tumor progression, with specificities that distinguish the functions of Rac3 from the established functions of Rac1 in these processes. Here, results highlighting the importance of Rac3 in distinct aspects of neuronal development and tumor cell biology are presented, in support of the non-redundant role of different members of the two Rac GTPases in physiological and pathological processes. MDPI 2019-09-11 /pmc/articles/PMC6770886/ /pubmed/31514269 http://dx.doi.org/10.3390/cells8091063 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
de Curtis, Ivan
The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title_full The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title_fullStr The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title_full_unstemmed The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title_short The Rac3 GTPase in Neuronal Development, Neurodevelopmental Disorders, and Cancer
title_sort rac3 gtpase in neuronal development, neurodevelopmental disorders, and cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770886/
https://www.ncbi.nlm.nih.gov/pubmed/31514269
http://dx.doi.org/10.3390/cells8091063
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