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Discordant evolution of mitochondrial and nuclear yeast genomes at population level

BACKGROUND: Mitochondria are essential organelles partially regulated by their own genomes. The mitochondrial genome maintenance and inheritance differ from the nuclear genome, potentially uncoupling their evolutionary trajectories. Here, we analysed mitochondrial sequences obtained from the 1011 Sa...

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Autores principales: De Chiara, Matteo, Friedrich, Anne, Barré, Benjamin, Breitenbach, Michael, Schacherer, Joseph, Liti, Gianni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216626/
https://www.ncbi.nlm.nih.gov/pubmed/32393264
http://dx.doi.org/10.1186/s12915-020-00786-4
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author De Chiara, Matteo
Friedrich, Anne
Barré, Benjamin
Breitenbach, Michael
Schacherer, Joseph
Liti, Gianni
author_facet De Chiara, Matteo
Friedrich, Anne
Barré, Benjamin
Breitenbach, Michael
Schacherer, Joseph
Liti, Gianni
author_sort De Chiara, Matteo
collection PubMed
description BACKGROUND: Mitochondria are essential organelles partially regulated by their own genomes. The mitochondrial genome maintenance and inheritance differ from the nuclear genome, potentially uncoupling their evolutionary trajectories. Here, we analysed mitochondrial sequences obtained from the 1011 Saccharomyces cerevisiae strain collection and identified pronounced differences with their nuclear genome counterparts. RESULTS: In contrast with pre-whole genome duplication fungal species, S. cerevisiae mitochondrial genomes show higher genetic diversity compared to the nuclear genomes. Strikingly, mitochondrial genomes appear to be highly admixed, resulting in a complex interconnected phylogeny with a weak grouping of isolates, whereas interspecies introgressions are very rare. Complete genome assemblies revealed that structural rearrangements are nearly absent with rare inversions detected. We tracked intron variation in COX1 and COB to infer gain and loss events throughout the species evolutionary history. Mitochondrial genome copy number is connected with the nuclear genome and linearly scale up with ploidy. We observed rare cases of naturally occurring mitochondrial DNA loss, petite, with a subset of them that do not suffer the expected growth defect in fermentable rich media. CONCLUSIONS: Overall, our results illustrate how differences in the biology of two genomes coexisting in the same cells can lead to discordant evolutionary histories.
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spelling pubmed-72166262020-05-18 Discordant evolution of mitochondrial and nuclear yeast genomes at population level De Chiara, Matteo Friedrich, Anne Barré, Benjamin Breitenbach, Michael Schacherer, Joseph Liti, Gianni BMC Biol Research Article BACKGROUND: Mitochondria are essential organelles partially regulated by their own genomes. The mitochondrial genome maintenance and inheritance differ from the nuclear genome, potentially uncoupling their evolutionary trajectories. Here, we analysed mitochondrial sequences obtained from the 1011 Saccharomyces cerevisiae strain collection and identified pronounced differences with their nuclear genome counterparts. RESULTS: In contrast with pre-whole genome duplication fungal species, S. cerevisiae mitochondrial genomes show higher genetic diversity compared to the nuclear genomes. Strikingly, mitochondrial genomes appear to be highly admixed, resulting in a complex interconnected phylogeny with a weak grouping of isolates, whereas interspecies introgressions are very rare. Complete genome assemblies revealed that structural rearrangements are nearly absent with rare inversions detected. We tracked intron variation in COX1 and COB to infer gain and loss events throughout the species evolutionary history. Mitochondrial genome copy number is connected with the nuclear genome and linearly scale up with ploidy. We observed rare cases of naturally occurring mitochondrial DNA loss, petite, with a subset of them that do not suffer the expected growth defect in fermentable rich media. CONCLUSIONS: Overall, our results illustrate how differences in the biology of two genomes coexisting in the same cells can lead to discordant evolutionary histories. BioMed Central 2020-05-11 /pmc/articles/PMC7216626/ /pubmed/32393264 http://dx.doi.org/10.1186/s12915-020-00786-4 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
De Chiara, Matteo
Friedrich, Anne
Barré, Benjamin
Breitenbach, Michael
Schacherer, Joseph
Liti, Gianni
Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title_full Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title_fullStr Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title_full_unstemmed Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title_short Discordant evolution of mitochondrial and nuclear yeast genomes at population level
title_sort discordant evolution of mitochondrial and nuclear yeast genomes at population level
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216626/
https://www.ncbi.nlm.nih.gov/pubmed/32393264
http://dx.doi.org/10.1186/s12915-020-00786-4
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