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Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates

Phototrophic eukaryotes have evolved mainly by the primary or secondary uptake of photosynthetic organisms. A return to heterotrophy occurred multiple times in various protistan groups such as Chrysophyceae, despite the expected advantage of autotrophy. It is assumed that the evolutionary shift to m...

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Autores principales: Majda, Stephan, Beisser, Daniela, Boenigk, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954800/
https://www.ncbi.nlm.nih.gov/pubmed/33712682
http://dx.doi.org/10.1038/s42003-021-01781-3
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author Majda, Stephan
Beisser, Daniela
Boenigk, Jens
author_facet Majda, Stephan
Beisser, Daniela
Boenigk, Jens
author_sort Majda, Stephan
collection PubMed
description Phototrophic eukaryotes have evolved mainly by the primary or secondary uptake of photosynthetic organisms. A return to heterotrophy occurred multiple times in various protistan groups such as Chrysophyceae, despite the expected advantage of autotrophy. It is assumed that the evolutionary shift to mixotrophy and further to heterotrophy is triggered by a differential importance of nutrient and carbon limitation. We sequenced the genomes of 16 chrysophyte strains and compared them in terms of size, function, and sequence characteristics in relation to photo-, mixo- and heterotrophic nutrition. All strains were sequenced with Illumina and partly with PacBio. Heterotrophic taxa have reduced genomes and a higher GC content of up to 59% as compared to phototrophic taxa. Heterotrophs have a large pan genome, but a small core genome, indicating a differential specialization of the distinct lineages. The pan genome of mixotrophs and heterotrophs taken together but not the pan genome of the mixotrophs alone covers the complete functionality of the phototrophic strains indicating a random reduction of genes. The observed ploidy ranges from di- to tetraploidy and was found to be independent of taxonomy or trophic mode. Our results substantiate an evolution driven by nutrient and carbon limitation.
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spelling pubmed-79548002021-03-28 Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates Majda, Stephan Beisser, Daniela Boenigk, Jens Commun Biol Article Phototrophic eukaryotes have evolved mainly by the primary or secondary uptake of photosynthetic organisms. A return to heterotrophy occurred multiple times in various protistan groups such as Chrysophyceae, despite the expected advantage of autotrophy. It is assumed that the evolutionary shift to mixotrophy and further to heterotrophy is triggered by a differential importance of nutrient and carbon limitation. We sequenced the genomes of 16 chrysophyte strains and compared them in terms of size, function, and sequence characteristics in relation to photo-, mixo- and heterotrophic nutrition. All strains were sequenced with Illumina and partly with PacBio. Heterotrophic taxa have reduced genomes and a higher GC content of up to 59% as compared to phototrophic taxa. Heterotrophs have a large pan genome, but a small core genome, indicating a differential specialization of the distinct lineages. The pan genome of mixotrophs and heterotrophs taken together but not the pan genome of the mixotrophs alone covers the complete functionality of the phototrophic strains indicating a random reduction of genes. The observed ploidy ranges from di- to tetraploidy and was found to be independent of taxonomy or trophic mode. Our results substantiate an evolution driven by nutrient and carbon limitation. Nature Publishing Group UK 2021-03-12 /pmc/articles/PMC7954800/ /pubmed/33712682 http://dx.doi.org/10.1038/s42003-021-01781-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Majda, Stephan
Beisser, Daniela
Boenigk, Jens
Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title_full Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title_fullStr Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title_full_unstemmed Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title_short Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
title_sort nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954800/
https://www.ncbi.nlm.nih.gov/pubmed/33712682
http://dx.doi.org/10.1038/s42003-021-01781-3
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