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Vav family exchange factors: an integrated regulatory and functional view

The Vav family is a group of tyrosine phosphorylation-regulated signal transduction molecules hierarchically located downstream of protein tyrosine kinases. The main function of these proteins is to work as guanosine nucleotide exchange factors (GEFs) for members of the Rho GTPase family. In additio...

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Autor principal: Bustelo, Xosé R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601183/
https://www.ncbi.nlm.nih.gov/pubmed/25483299
http://dx.doi.org/10.4161/21541248.2014.973757
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author Bustelo, Xosé R
author_facet Bustelo, Xosé R
author_sort Bustelo, Xosé R
collection PubMed
description The Vav family is a group of tyrosine phosphorylation-regulated signal transduction molecules hierarchically located downstream of protein tyrosine kinases. The main function of these proteins is to work as guanosine nucleotide exchange factors (GEFs) for members of the Rho GTPase family. In addition, they can exhibit a variety of catalysis-independent roles in specific signaling contexts. Vav proteins play essential signaling roles for both the development and/or effector functions of a large variety of cell lineages, including those belonging to the immune, nervous, and cardiovascular systems. They also contribute to pathological states such as cancer, immune-related dysfunctions, and atherosclerosis. Here, I will provide an integrated view about the evolution, regulation, and effector properties of these signaling molecules. In addition, I will discuss the pros and cons for their potential consideration as therapeutic targets.
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spelling pubmed-46011832016-02-03 Vav family exchange factors: an integrated regulatory and functional view Bustelo, Xosé R Small GTPases Review The Vav family is a group of tyrosine phosphorylation-regulated signal transduction molecules hierarchically located downstream of protein tyrosine kinases. The main function of these proteins is to work as guanosine nucleotide exchange factors (GEFs) for members of the Rho GTPase family. In addition, they can exhibit a variety of catalysis-independent roles in specific signaling contexts. Vav proteins play essential signaling roles for both the development and/or effector functions of a large variety of cell lineages, including those belonging to the immune, nervous, and cardiovascular systems. They also contribute to pathological states such as cancer, immune-related dysfunctions, and atherosclerosis. Here, I will provide an integrated view about the evolution, regulation, and effector properties of these signaling molecules. In addition, I will discuss the pros and cons for their potential consideration as therapeutic targets. Taylor & Francis 2014-11-17 /pmc/articles/PMC4601183/ /pubmed/25483299 http://dx.doi.org/10.4161/21541248.2014.973757 Text en © 2014 The Author(s). Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Review
Bustelo, Xosé R
Vav family exchange factors: an integrated regulatory and functional view
title Vav family exchange factors: an integrated regulatory and functional view
title_full Vav family exchange factors: an integrated regulatory and functional view
title_fullStr Vav family exchange factors: an integrated regulatory and functional view
title_full_unstemmed Vav family exchange factors: an integrated regulatory and functional view
title_short Vav family exchange factors: an integrated regulatory and functional view
title_sort vav family exchange factors: an integrated regulatory and functional view
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601183/
https://www.ncbi.nlm.nih.gov/pubmed/25483299
http://dx.doi.org/10.4161/21541248.2014.973757
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