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High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing

Genetic variation in natural populations represents the raw material for phenotypic diversity. Species-wide characterization of genetic variants is crucial to have a deeper insight into the genotype-phenotype relationship. With the advent of new sequencing strategies and more recently the release of...

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Autores principales: Fournier, Téo, Gounot, Jean-Sébastien, Freel, Kelle, Cruaud, Corinne, Lemainque, Arnaud, Aury, Jean-Marc, Wincker, Patrick, Schacherer, Joseph, Friedrich, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633375/
https://www.ncbi.nlm.nih.gov/pubmed/28983066
http://dx.doi.org/10.1534/g3.117.300128
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author Fournier, Téo
Gounot, Jean-Sébastien
Freel, Kelle
Cruaud, Corinne
Lemainque, Arnaud
Aury, Jean-Marc
Wincker, Patrick
Schacherer, Joseph
Friedrich, Anne
author_facet Fournier, Téo
Gounot, Jean-Sébastien
Freel, Kelle
Cruaud, Corinne
Lemainque, Arnaud
Aury, Jean-Marc
Wincker, Patrick
Schacherer, Joseph
Friedrich, Anne
author_sort Fournier, Téo
collection PubMed
description Genetic variation in natural populations represents the raw material for phenotypic diversity. Species-wide characterization of genetic variants is crucial to have a deeper insight into the genotype-phenotype relationship. With the advent of new sequencing strategies and more recently the release of long-read sequencing platforms, it is now possible to explore the genetic diversity of any nonmodel organisms, representing a fundamental resource for biological research. In the frame of population genomic surveys, a first step is to obtain the complete sequence and high-quality assembly of a reference genome. Here, we sequenced and assembled a reference genome of the nonconventional Dekkera bruxellensis yeast. While this species is a major cause of wine spoilage, it paradoxically contributes to the specific flavor profile of some Belgium beers. In addition, an extreme karyotype variability is observed across natural isolates, highlighting that D. bruxellensis genome is very dynamic. The whole genome of the D. bruxellensis UMY321 isolate was sequenced using a combination of Nanopore long-read and Illumina short-read sequencing data. We generated the most complete and contiguous de novo assembly of D. bruxellensis to date and obtained a first glimpse into the genomic variability within this species by comparing the sequences of several isolates. This genome sequence is therefore of high value for population genomic surveys and represents a reference to study genome dynamic in this yeast species.
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spelling pubmed-56333752017-10-18 High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing Fournier, Téo Gounot, Jean-Sébastien Freel, Kelle Cruaud, Corinne Lemainque, Arnaud Aury, Jean-Marc Wincker, Patrick Schacherer, Joseph Friedrich, Anne G3 (Bethesda) Genome Report Genetic variation in natural populations represents the raw material for phenotypic diversity. Species-wide characterization of genetic variants is crucial to have a deeper insight into the genotype-phenotype relationship. With the advent of new sequencing strategies and more recently the release of long-read sequencing platforms, it is now possible to explore the genetic diversity of any nonmodel organisms, representing a fundamental resource for biological research. In the frame of population genomic surveys, a first step is to obtain the complete sequence and high-quality assembly of a reference genome. Here, we sequenced and assembled a reference genome of the nonconventional Dekkera bruxellensis yeast. While this species is a major cause of wine spoilage, it paradoxically contributes to the specific flavor profile of some Belgium beers. In addition, an extreme karyotype variability is observed across natural isolates, highlighting that D. bruxellensis genome is very dynamic. The whole genome of the D. bruxellensis UMY321 isolate was sequenced using a combination of Nanopore long-read and Illumina short-read sequencing data. We generated the most complete and contiguous de novo assembly of D. bruxellensis to date and obtained a first glimpse into the genomic variability within this species by comparing the sequences of several isolates. This genome sequence is therefore of high value for population genomic surveys and represents a reference to study genome dynamic in this yeast species. Genetics Society of America 2017-08-09 /pmc/articles/PMC5633375/ /pubmed/28983066 http://dx.doi.org/10.1534/g3.117.300128 Text en Copyright © 2017 Fournier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Fournier, Téo
Gounot, Jean-Sébastien
Freel, Kelle
Cruaud, Corinne
Lemainque, Arnaud
Aury, Jean-Marc
Wincker, Patrick
Schacherer, Joseph
Friedrich, Anne
High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title_full High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title_fullStr High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title_full_unstemmed High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title_short High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing
title_sort high-quality de novo genome assembly of the dekkera bruxellensis yeast using nanopore minion sequencing
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633375/
https://www.ncbi.nlm.nih.gov/pubmed/28983066
http://dx.doi.org/10.1534/g3.117.300128
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