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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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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. |
format | Online Article Text |
id | pubmed-8923023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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