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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5462543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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