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Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton
Emiliania huxleyi is the most abundant calcifying plankton in modern oceans with substantial intraspecific genome variability and a biphasic life cycle involving sexual alternation between calcified 2N and flagellated 1N cells. We show that high genome content variability in Emiliania relates to ero...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438323/ https://www.ncbi.nlm.nih.gov/pubmed/25461969 http://dx.doi.org/10.1038/ismej.2014.221 |
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author | von Dassow, Peter John, Uwe Ogata, Hiroyuki Probert, Ian Bendif, El Mahdi Kegel, Jessica U Audic, Stéphane Wincker, Patrick Da Silva, Corinne Claverie, Jean-Michel Doney, Scott Glover, David M Flores, Daniella Mella Herrera, Yeritza Lescot, Magali Garet-Delmas, Marie-José de Vargas, Colomban |
author_facet | von Dassow, Peter John, Uwe Ogata, Hiroyuki Probert, Ian Bendif, El Mahdi Kegel, Jessica U Audic, Stéphane Wincker, Patrick Da Silva, Corinne Claverie, Jean-Michel Doney, Scott Glover, David M Flores, Daniella Mella Herrera, Yeritza Lescot, Magali Garet-Delmas, Marie-José de Vargas, Colomban |
author_sort | von Dassow, Peter |
collection | PubMed |
description | Emiliania huxleyi is the most abundant calcifying plankton in modern oceans with substantial intraspecific genome variability and a biphasic life cycle involving sexual alternation between calcified 2N and flagellated 1N cells. We show that high genome content variability in Emiliania relates to erosion of 1N-specific genes and loss of the ability to form flagellated cells. Analysis of 185 E. huxleyi strains isolated from world oceans suggests that loss of flagella occurred independently in lineages inhabiting oligotrophic open oceans over short evolutionary timescales. This environmentally linked physiogenomic change suggests life cycling is not advantageous in very large/diluted populations experiencing low biotic pressure and low ecological variability. Gene loss did not appear to reflect pressure for genome streamlining in oligotrophic oceans as previously observed in picoplankton. Life-cycle modifications might be common in plankton and cause major functional variability to be hidden from traditional taxonomic or molecular markers. |
format | Online Article Text |
id | pubmed-4438323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44383232015-06-01 Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton von Dassow, Peter John, Uwe Ogata, Hiroyuki Probert, Ian Bendif, El Mahdi Kegel, Jessica U Audic, Stéphane Wincker, Patrick Da Silva, Corinne Claverie, Jean-Michel Doney, Scott Glover, David M Flores, Daniella Mella Herrera, Yeritza Lescot, Magali Garet-Delmas, Marie-José de Vargas, Colomban ISME J Original Article Emiliania huxleyi is the most abundant calcifying plankton in modern oceans with substantial intraspecific genome variability and a biphasic life cycle involving sexual alternation between calcified 2N and flagellated 1N cells. We show that high genome content variability in Emiliania relates to erosion of 1N-specific genes and loss of the ability to form flagellated cells. Analysis of 185 E. huxleyi strains isolated from world oceans suggests that loss of flagella occurred independently in lineages inhabiting oligotrophic open oceans over short evolutionary timescales. This environmentally linked physiogenomic change suggests life cycling is not advantageous in very large/diluted populations experiencing low biotic pressure and low ecological variability. Gene loss did not appear to reflect pressure for genome streamlining in oligotrophic oceans as previously observed in picoplankton. Life-cycle modifications might be common in plankton and cause major functional variability to be hidden from traditional taxonomic or molecular markers. Nature Publishing Group 2015-06 2014-12-02 /pmc/articles/PMC4438323/ /pubmed/25461969 http://dx.doi.org/10.1038/ismej.2014.221 Text en Copyright © 2015 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article von Dassow, Peter John, Uwe Ogata, Hiroyuki Probert, Ian Bendif, El Mahdi Kegel, Jessica U Audic, Stéphane Wincker, Patrick Da Silva, Corinne Claverie, Jean-Michel Doney, Scott Glover, David M Flores, Daniella Mella Herrera, Yeritza Lescot, Magali Garet-Delmas, Marie-José de Vargas, Colomban Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title | Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title_full | Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title_fullStr | Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title_full_unstemmed | Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title_short | Life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
title_sort | life-cycle modification in open oceans accounts for genome variability in a cosmopolitan phytoplankton |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438323/ https://www.ncbi.nlm.nih.gov/pubmed/25461969 http://dx.doi.org/10.1038/ismej.2014.221 |
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