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Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System
The membrane trafficking is an essential process of eukaryotic cells, as it manages vesicular trafficking toward different parts of the cell. In this process, membrane fusions between vesicles and target membranes are mediated by several factors, including the multisubunit tethering complexes. One t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290106/ https://www.ncbi.nlm.nih.gov/pubmed/34061181 http://dx.doi.org/10.1093/gbe/evab125 |
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author | Santana-Molina, Carlos Gutierrez, Fernando Devos, Damien P |
author_facet | Santana-Molina, Carlos Gutierrez, Fernando Devos, Damien P |
author_sort | Santana-Molina, Carlos |
collection | PubMed |
description | The membrane trafficking is an essential process of eukaryotic cells, as it manages vesicular trafficking toward different parts of the cell. In this process, membrane fusions between vesicles and target membranes are mediated by several factors, including the multisubunit tethering complexes. One type of multisubunit tethering complex, the complexes associated with tethering containing helical rods (CATCHR), encompasses the exocyst, COG, GARP, and DSL1 complexes. The CATCHR share similarities at sequence, structural, and protein-complex organization level although their actual relationship is still poorly understood. In this study, we have re-evaluated CATCHR at different levels, demonstrating that gene duplications followed by neofunctionalization, were key for their origin. Our results, reveals that there are specific homology relationships and parallelism within and between the CATCHR suggesting that most of these complexes are composed by modular tetramers of four different kinds of proteins, three of them having a clear common origin. The extension of CATCHR family occurred concomitantly with the protein family expansions of their molecular partners, such as small GTPases and SNAREs, among others, and likely providing functional specificity. Our results provide novel insights into the structural organization and mechanism of action of CATCHR, with implications for the evolution of the endomembrane system of eukaryotes and promoting CATCHR as ideal candidates to study the evolution of multiprotein complexes. |
format | Online Article Text |
id | pubmed-8290106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82901062021-07-21 Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System Santana-Molina, Carlos Gutierrez, Fernando Devos, Damien P Genome Biol Evol Research Article The membrane trafficking is an essential process of eukaryotic cells, as it manages vesicular trafficking toward different parts of the cell. In this process, membrane fusions between vesicles and target membranes are mediated by several factors, including the multisubunit tethering complexes. One type of multisubunit tethering complex, the complexes associated with tethering containing helical rods (CATCHR), encompasses the exocyst, COG, GARP, and DSL1 complexes. The CATCHR share similarities at sequence, structural, and protein-complex organization level although their actual relationship is still poorly understood. In this study, we have re-evaluated CATCHR at different levels, demonstrating that gene duplications followed by neofunctionalization, were key for their origin. Our results, reveals that there are specific homology relationships and parallelism within and between the CATCHR suggesting that most of these complexes are composed by modular tetramers of four different kinds of proteins, three of them having a clear common origin. The extension of CATCHR family occurred concomitantly with the protein family expansions of their molecular partners, such as small GTPases and SNAREs, among others, and likely providing functional specificity. Our results provide novel insights into the structural organization and mechanism of action of CATCHR, with implications for the evolution of the endomembrane system of eukaryotes and promoting CATCHR as ideal candidates to study the evolution of multiprotein complexes. Oxford University Press 2021-06-01 /pmc/articles/PMC8290106/ /pubmed/34061181 http://dx.doi.org/10.1093/gbe/evab125 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Santana-Molina, Carlos Gutierrez, Fernando Devos, Damien P Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title | Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title_full | Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title_fullStr | Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title_full_unstemmed | Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title_short | Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System |
title_sort | homology and modular evolution of catchr at the origin of the eukaryotic endomembrane system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290106/ https://www.ncbi.nlm.nih.gov/pubmed/34061181 http://dx.doi.org/10.1093/gbe/evab125 |
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