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Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation

Parasite surfaces support multiple functions required for survival within their hosts, and maintenance and functionality of the surface depends on membrane trafficking. To understand the evolutionary history of trypanosomatid trafficking, where multiple lifestyles and mechanisms of host interactions...

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Autores principales: Venkatesh, Divya, Boehm, Cordula, Barlow, Lael D., Nankissoor, Nerissa N., O'Reilly, Amanda, Kelly, Steven, Dacks, Joel B., Field, Mark C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399786/
https://www.ncbi.nlm.nih.gov/pubmed/28386020
http://dx.doi.org/10.1242/jcs.197640
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author Venkatesh, Divya
Boehm, Cordula
Barlow, Lael D.
Nankissoor, Nerissa N.
O'Reilly, Amanda
Kelly, Steven
Dacks, Joel B.
Field, Mark C.
author_facet Venkatesh, Divya
Boehm, Cordula
Barlow, Lael D.
Nankissoor, Nerissa N.
O'Reilly, Amanda
Kelly, Steven
Dacks, Joel B.
Field, Mark C.
author_sort Venkatesh, Divya
collection PubMed
description Parasite surfaces support multiple functions required for survival within their hosts, and maintenance and functionality of the surface depends on membrane trafficking. To understand the evolutionary history of trypanosomatid trafficking, where multiple lifestyles and mechanisms of host interactions are known, we examined protein families central to defining intracellular compartments and mediating transport, namely Rabs, SNAREs and RabGAPs, across all available Euglenozoa genomes. Bodonids possess a large trafficking repertoire, which is mainly retained by the Trypanosoma cruzi group, with extensive losses in other lineages, particularly African trypanosomes and phytomonads. There are no large-scale expansions or contractions from an inferred ancestor, excluding direct associations between parasitism or host range. However, we observe stepwise secondary losses within Rab and SNARE cohorts (but not RabGAPs). Major changes are associated with endosomal and late exocytic pathways, consistent with the diversity in surface proteomes between trypanosomatids and mechanisms of interaction with the host. Along with the conserved core family proteins, several lineage-specific members of the Rab (but not SNARE) family were found. Significantly, testing predictions of SNARE complex composition by proteomics confirms generalised retention of function across eukaryotes.
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spelling pubmed-53997862017-05-16 Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation Venkatesh, Divya Boehm, Cordula Barlow, Lael D. Nankissoor, Nerissa N. O'Reilly, Amanda Kelly, Steven Dacks, Joel B. Field, Mark C. J Cell Sci Research Article Parasite surfaces support multiple functions required for survival within their hosts, and maintenance and functionality of the surface depends on membrane trafficking. To understand the evolutionary history of trypanosomatid trafficking, where multiple lifestyles and mechanisms of host interactions are known, we examined protein families central to defining intracellular compartments and mediating transport, namely Rabs, SNAREs and RabGAPs, across all available Euglenozoa genomes. Bodonids possess a large trafficking repertoire, which is mainly retained by the Trypanosoma cruzi group, with extensive losses in other lineages, particularly African trypanosomes and phytomonads. There are no large-scale expansions or contractions from an inferred ancestor, excluding direct associations between parasitism or host range. However, we observe stepwise secondary losses within Rab and SNARE cohorts (but not RabGAPs). Major changes are associated with endosomal and late exocytic pathways, consistent with the diversity in surface proteomes between trypanosomatids and mechanisms of interaction with the host. Along with the conserved core family proteins, several lineage-specific members of the Rab (but not SNARE) family were found. Significantly, testing predictions of SNARE complex composition by proteomics confirms generalised retention of function across eukaryotes. The Company of Biologists Ltd 2017-04-15 /pmc/articles/PMC5399786/ /pubmed/28386020 http://dx.doi.org/10.1242/jcs.197640 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Venkatesh, Divya
Boehm, Cordula
Barlow, Lael D.
Nankissoor, Nerissa N.
O'Reilly, Amanda
Kelly, Steven
Dacks, Joel B.
Field, Mark C.
Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title_full Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title_fullStr Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title_full_unstemmed Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title_short Evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
title_sort evolution of the endomembrane systems of trypanosomatids – conservation and specialisation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399786/
https://www.ncbi.nlm.nih.gov/pubmed/28386020
http://dx.doi.org/10.1242/jcs.197640
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