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Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome

Plastids are supported by a wide range of proteins encoded within the nucleus and imported from the cytoplasm. These plastid-targeted proteins may originate from the endosymbiont, the host, or other sources entirely. Here, we identify and characterise 770 plastid-targeted proteins that are conserved...

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Autores principales: Dorrell, Richard G, Gile, Gillian, McCallum, Giselle, Méheust, Raphaël, Bapteste, Eric P, Klinger, Christen M, Brillet-Guéguen, Loraine, Freeman, Katalina D, Richter, Daniel J, Bowler, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462543/
https://www.ncbi.nlm.nih.gov/pubmed/28498102
http://dx.doi.org/10.7554/eLife.23717
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author Dorrell, Richard G
Gile, Gillian
McCallum, Giselle
Méheust, Raphaël
Bapteste, Eric P
Klinger, Christen M
Brillet-Guéguen, Loraine
Freeman, Katalina D
Richter, Daniel J
Bowler, Chris
author_facet Dorrell, Richard G
Gile, Gillian
McCallum, Giselle
Méheust, Raphaël
Bapteste, Eric P
Klinger, Christen M
Brillet-Guéguen, Loraine
Freeman, Katalina D
Richter, Daniel J
Bowler, Chris
author_sort Dorrell, Richard G
collection PubMed
description Plastids are supported by a wide range of proteins encoded within the nucleus and imported from the cytoplasm. These plastid-targeted proteins may originate from the endosymbiont, the host, or other sources entirely. Here, we identify and characterise 770 plastid-targeted proteins that are conserved across the ochrophytes, a major group of algae including diatoms, pelagophytes and kelps, that possess plastids derived from red algae. We show that the ancestral ochrophyte plastid proteome was an evolutionary chimera, with 25% of its phylogenetically tractable nucleus-encoded proteins deriving from green algae. We additionally show that functional mixing of host and plastid proteomes, such as through dual-targeting, is an ancestral feature of plastid evolution. Finally, we detect a clear phylogenetic signal from one ochrophyte subgroup, the lineage containing pelagophytes and dictyochophytes, in plastid-targeted proteins from another major algal lineage, the haptophytes. This may represent a possible serial endosymbiosis event deep in eukaryotic evolutionary history. DOI: http://dx.doi.org/10.7554/eLife.23717.001
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spelling pubmed-54625432017-06-09 Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome Dorrell, Richard G Gile, Gillian McCallum, Giselle Méheust, Raphaël Bapteste, Eric P Klinger, Christen M Brillet-Guéguen, Loraine Freeman, Katalina D Richter, Daniel J Bowler, Chris eLife Cell Biology Plastids are supported by a wide range of proteins encoded within the nucleus and imported from the cytoplasm. These plastid-targeted proteins may originate from the endosymbiont, the host, or other sources entirely. Here, we identify and characterise 770 plastid-targeted proteins that are conserved across the ochrophytes, a major group of algae including diatoms, pelagophytes and kelps, that possess plastids derived from red algae. We show that the ancestral ochrophyte plastid proteome was an evolutionary chimera, with 25% of its phylogenetically tractable nucleus-encoded proteins deriving from green algae. We additionally show that functional mixing of host and plastid proteomes, such as through dual-targeting, is an ancestral feature of plastid evolution. Finally, we detect a clear phylogenetic signal from one ochrophyte subgroup, the lineage containing pelagophytes and dictyochophytes, in plastid-targeted proteins from another major algal lineage, the haptophytes. This may represent a possible serial endosymbiosis event deep in eukaryotic evolutionary history. DOI: http://dx.doi.org/10.7554/eLife.23717.001 eLife Sciences Publications, Ltd 2017-05-12 /pmc/articles/PMC5462543/ /pubmed/28498102 http://dx.doi.org/10.7554/eLife.23717 Text en © 2017, Dorrell et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Dorrell, Richard G
Gile, Gillian
McCallum, Giselle
Méheust, Raphaël
Bapteste, Eric P
Klinger, Christen M
Brillet-Guéguen, Loraine
Freeman, Katalina D
Richter, Daniel J
Bowler, Chris
Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title_full Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title_fullStr Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title_full_unstemmed Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title_short Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
title_sort chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462543/
https://www.ncbi.nlm.nih.gov/pubmed/28498102
http://dx.doi.org/10.7554/eLife.23717
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