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Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators

GTP binding proteins known as small GTPases make up one of the largest groups of regulatory proteins and control almost all functions of living cells. Their activity is under, respectively, positive and negative regulation by guanine nucleotide exchange factors (GEFs) and GTPase activating proteins...

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Autores principales: Forbes, Gillian, Schilde, Christina, Lawal, Hajara, Kin, Koryu, Du, Qingyou, Chen, Zhi-hui, Rivero, Francisco, Schaap, Pauline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923023/
https://www.ncbi.nlm.nih.gov/pubmed/34565293
http://dx.doi.org/10.1080/21541248.2021.1984829
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author Forbes, Gillian
Schilde, Christina
Lawal, Hajara
Kin, Koryu
Du, Qingyou
Chen, Zhi-hui
Rivero, Francisco
Schaap, Pauline
author_facet Forbes, Gillian
Schilde, Christina
Lawal, Hajara
Kin, Koryu
Du, Qingyou
Chen, Zhi-hui
Rivero, Francisco
Schaap, Pauline
author_sort Forbes, Gillian
collection PubMed
description GTP binding proteins known as small GTPases make up one of the largest groups of regulatory proteins and control almost all functions of living cells. Their activity is under, respectively, positive and negative regulation by guanine nucleotide exchange factors (GEFs) and GTPase activating proteins (GAPs), which together with their upstream regulators and the downstream targets of the small GTPases form formidable signalling networks. While genomics has revealed the large size of the GTPase, GEF and GAP repertoires, only a small fraction of their interactions and functions have yet been experimentally explored. Dictyostelid social amoebas have been particularly useful in unravelling the roles of many proteins in the Rac-Rho and Ras-Rap families of GTPases in directional cell migration and regulation of the actin cytoskeleton. Genomes and cell-type specific and developmental transcriptomes are available for Dictyostelium species that span the 0.5 billion years of evolution of the group from their unicellular ancestors. In this work, we identified all GTPases, GEFs and GAPs from genomes representative of the four major taxon groups and investigated their phylogenetic relationships and evolutionary conservation and changes in their functional domain architecture and in their developmental and cell-type specific expression. We performed a hierarchical cluster analysis of the expression profiles of the ~2000 analysed genes to identify putative interacting sets of GTPases, GEFs and GAPs, which highlight sets known to interact experimentally and many novel combinations. This work represents a valuable resource for research into all fields of cellular regulation.
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spelling pubmed-89230232022-03-16 Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators Forbes, Gillian Schilde, Christina Lawal, Hajara Kin, Koryu Du, Qingyou Chen, Zhi-hui Rivero, Francisco Schaap, Pauline Small GTPases Research Paper GTP binding proteins known as small GTPases make up one of the largest groups of regulatory proteins and control almost all functions of living cells. Their activity is under, respectively, positive and negative regulation by guanine nucleotide exchange factors (GEFs) and GTPase activating proteins (GAPs), which together with their upstream regulators and the downstream targets of the small GTPases form formidable signalling networks. While genomics has revealed the large size of the GTPase, GEF and GAP repertoires, only a small fraction of their interactions and functions have yet been experimentally explored. Dictyostelid social amoebas have been particularly useful in unravelling the roles of many proteins in the Rac-Rho and Ras-Rap families of GTPases in directional cell migration and regulation of the actin cytoskeleton. Genomes and cell-type specific and developmental transcriptomes are available for Dictyostelium species that span the 0.5 billion years of evolution of the group from their unicellular ancestors. In this work, we identified all GTPases, GEFs and GAPs from genomes representative of the four major taxon groups and investigated their phylogenetic relationships and evolutionary conservation and changes in their functional domain architecture and in their developmental and cell-type specific expression. We performed a hierarchical cluster analysis of the expression profiles of the ~2000 analysed genes to identify putative interacting sets of GTPases, GEFs and GAPs, which highlight sets known to interact experimentally and many novel combinations. This work represents a valuable resource for research into all fields of cellular regulation. Taylor & Francis 2021-10-05 /pmc/articles/PMC8923023/ /pubmed/34565293 http://dx.doi.org/10.1080/21541248.2021.1984829 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Forbes, Gillian
Schilde, Christina
Lawal, Hajara
Kin, Koryu
Du, Qingyou
Chen, Zhi-hui
Rivero, Francisco
Schaap, Pauline
Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title_full Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title_fullStr Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title_full_unstemmed Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title_short Interactome and evolutionary conservation of Dictyostelid small GTPases and their direct regulators
title_sort interactome and evolutionary conservation of dictyostelid small gtpases and their direct regulators
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923023/
https://www.ncbi.nlm.nih.gov/pubmed/34565293
http://dx.doi.org/10.1080/21541248.2021.1984829
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