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High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population

Genome-wide characterization of genetic variants of a large population of individuals within the same species is essential to have a deeper insight into its evolutionary history as well as the genotype–phenotype relationship. Population genomic surveys have been performed in multiple yeast species,...

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Autores principales: Gounot, Jean-Sébastien, Neuvéglise, Cécile, Freel, Kelle C, Devillers, Hugo, Piškur, Jure, Friedrich, Anne, Schacherer, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313668/
https://www.ncbi.nlm.nih.gov/pubmed/32302403
http://dx.doi.org/10.1093/gbe/evaa077
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author Gounot, Jean-Sébastien
Neuvéglise, Cécile
Freel, Kelle C
Devillers, Hugo
Piškur, Jure
Friedrich, Anne
Schacherer, Joseph
author_facet Gounot, Jean-Sébastien
Neuvéglise, Cécile
Freel, Kelle C
Devillers, Hugo
Piškur, Jure
Friedrich, Anne
Schacherer, Joseph
author_sort Gounot, Jean-Sébastien
collection PubMed
description Genome-wide characterization of genetic variants of a large population of individuals within the same species is essential to have a deeper insight into its evolutionary history as well as the genotype–phenotype relationship. Population genomic surveys have been performed in multiple yeast species, including the two model organisms, Saccharomyces cerevisiae and Schizosaccharomyces pombe. In this context, we sought to characterize at the population level the Brettanomyces bruxellensis yeast species, which is a major cause of wine spoilage and can contribute to the specific flavor profile of some Belgium beers. We have completely sequenced the genome of 53 B. bruxellensis strains isolated worldwide. The annotation of the reference genome allowed us to define the gene content of this species. As previously suggested, our genomic data clearly highlighted that genetic diversity variation is related to ploidy level, which is variable in the B. bruxellensis species. Genomes are punctuated by multiple loss-of-heterozygosity regions, whereas aneuploidies as well as segmental duplications are uncommon. Interestingly, triploid genomes are more prone to gene copy number variation than diploids. Finally, the pangenome of the species was reconstructed and was found to be small with few accessory genes compared with S. cerevisiae. The pangenome is composed of 5,409 ORFs (open reading frames) among which 5,106 core ORFs and 303 ORFs that are variable within the population. All these results highlight the different trajectories of species evolution and consequently the interest of establishing population genomic surveys in more populations.
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spelling pubmed-73136682020-06-29 High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population Gounot, Jean-Sébastien Neuvéglise, Cécile Freel, Kelle C Devillers, Hugo Piškur, Jure Friedrich, Anne Schacherer, Joseph Genome Biol Evol Research Article Genome-wide characterization of genetic variants of a large population of individuals within the same species is essential to have a deeper insight into its evolutionary history as well as the genotype–phenotype relationship. Population genomic surveys have been performed in multiple yeast species, including the two model organisms, Saccharomyces cerevisiae and Schizosaccharomyces pombe. In this context, we sought to characterize at the population level the Brettanomyces bruxellensis yeast species, which is a major cause of wine spoilage and can contribute to the specific flavor profile of some Belgium beers. We have completely sequenced the genome of 53 B. bruxellensis strains isolated worldwide. The annotation of the reference genome allowed us to define the gene content of this species. As previously suggested, our genomic data clearly highlighted that genetic diversity variation is related to ploidy level, which is variable in the B. bruxellensis species. Genomes are punctuated by multiple loss-of-heterozygosity regions, whereas aneuploidies as well as segmental duplications are uncommon. Interestingly, triploid genomes are more prone to gene copy number variation than diploids. Finally, the pangenome of the species was reconstructed and was found to be small with few accessory genes compared with S. cerevisiae. The pangenome is composed of 5,409 ORFs (open reading frames) among which 5,106 core ORFs and 303 ORFs that are variable within the population. All these results highlight the different trajectories of species evolution and consequently the interest of establishing population genomic surveys in more populations. Oxford University Press 2020-04-22 /pmc/articles/PMC7313668/ /pubmed/32302403 http://dx.doi.org/10.1093/gbe/evaa077 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gounot, Jean-Sébastien
Neuvéglise, Cécile
Freel, Kelle C
Devillers, Hugo
Piškur, Jure
Friedrich, Anne
Schacherer, Joseph
High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title_full High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title_fullStr High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title_full_unstemmed High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title_short High Complexity and Degree of Genetic Variation in Brettanomyces bruxellensis Population
title_sort high complexity and degree of genetic variation in brettanomyces bruxellensis population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313668/
https://www.ncbi.nlm.nih.gov/pubmed/32302403
http://dx.doi.org/10.1093/gbe/evaa077
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