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Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes

BACKGROUND: The presence of low complexity and repeated regions in genomes often results in difficulties to assemble sequencing data into full chromosomes. However, the availability of full genome scaffolds is essential to several investigations, regarding for instance the evolution of entire clades...

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Autores principales: Jourdier, Etienne, Baudry, Lyam, Poggi-Parodi, Dante, Vicq, Yoan, Koszul, Romain, Margeot, Antoine, Marbouty, Martial, Bidard, Frédérique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469131/
https://www.ncbi.nlm.nih.gov/pubmed/28616075
http://dx.doi.org/10.1186/s13068-017-0837-6
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author Jourdier, Etienne
Baudry, Lyam
Poggi-Parodi, Dante
Vicq, Yoan
Koszul, Romain
Margeot, Antoine
Marbouty, Martial
Bidard, Frédérique
author_facet Jourdier, Etienne
Baudry, Lyam
Poggi-Parodi, Dante
Vicq, Yoan
Koszul, Romain
Margeot, Antoine
Marbouty, Martial
Bidard, Frédérique
author_sort Jourdier, Etienne
collection PubMed
description BACKGROUND: The presence of low complexity and repeated regions in genomes often results in difficulties to assemble sequencing data into full chromosomes. However, the availability of full genome scaffolds is essential to several investigations, regarding for instance the evolution of entire clades, the analysis of chromosome rearrangements, and is pivotal to sexual crossing studies. In non-conventional but industrially relevant model organisms, such as the ascomycete Trichoderma reesei, a complete genome assembly is seldom available. RESULTS: The chromosome scaffolds of T. reesei QM6a and Rut-C30 strains have been generated using a contact genomic/proximity ligation genomic approach. The original reference assembly, encompassing dozens of scaffolds, was reorganized into two sets of seven chromosomes. Chromosomal contact data also allowed to characterize 10–40 kb, gene-free, AT-rich (76%) regions corresponding to the T. reesei centromeres. Large chromosomal rearrangements (LCR) in Rut-C30 were then characterized, in agreement with former studies, and the position of LCR breakpoints used to assess the likely chromosome structure of other T. reesei strains [QM9414, CBS999.97 (1-1, re), and QM9978]. In agreement with published results, we predict that the numerous chromosome rearrangements found in highly mutated industrial strains may limit the efficiency of sexual reproduction for their improvement. CONCLUSIONS: The GRAAL program allowed us to generate the karyotype of the Rut-C30 strain, and from there to predict chromosome structure for most T. reesei strains for which sequence is available. This method that exploits proximity ligation sequencing approach is a fast, cheap, and straightforward way to characterize both chromosome structure and centromere sequences and is likely to represent a popular convenient alternative to expensive and work-intensive resequencing projects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0837-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-54691312017-06-14 Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes Jourdier, Etienne Baudry, Lyam Poggi-Parodi, Dante Vicq, Yoan Koszul, Romain Margeot, Antoine Marbouty, Martial Bidard, Frédérique Biotechnol Biofuels Research BACKGROUND: The presence of low complexity and repeated regions in genomes often results in difficulties to assemble sequencing data into full chromosomes. However, the availability of full genome scaffolds is essential to several investigations, regarding for instance the evolution of entire clades, the analysis of chromosome rearrangements, and is pivotal to sexual crossing studies. In non-conventional but industrially relevant model organisms, such as the ascomycete Trichoderma reesei, a complete genome assembly is seldom available. RESULTS: The chromosome scaffolds of T. reesei QM6a and Rut-C30 strains have been generated using a contact genomic/proximity ligation genomic approach. The original reference assembly, encompassing dozens of scaffolds, was reorganized into two sets of seven chromosomes. Chromosomal contact data also allowed to characterize 10–40 kb, gene-free, AT-rich (76%) regions corresponding to the T. reesei centromeres. Large chromosomal rearrangements (LCR) in Rut-C30 were then characterized, in agreement with former studies, and the position of LCR breakpoints used to assess the likely chromosome structure of other T. reesei strains [QM9414, CBS999.97 (1-1, re), and QM9978]. In agreement with published results, we predict that the numerous chromosome rearrangements found in highly mutated industrial strains may limit the efficiency of sexual reproduction for their improvement. CONCLUSIONS: The GRAAL program allowed us to generate the karyotype of the Rut-C30 strain, and from there to predict chromosome structure for most T. reesei strains for which sequence is available. This method that exploits proximity ligation sequencing approach is a fast, cheap, and straightforward way to characterize both chromosome structure and centromere sequences and is likely to represent a popular convenient alternative to expensive and work-intensive resequencing projects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0837-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-12 /pmc/articles/PMC5469131/ /pubmed/28616075 http://dx.doi.org/10.1186/s13068-017-0837-6 Text en © The Author(s) 2017 Open AccessThis article is 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 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 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.
spellingShingle Research
Jourdier, Etienne
Baudry, Lyam
Poggi-Parodi, Dante
Vicq, Yoan
Koszul, Romain
Margeot, Antoine
Marbouty, Martial
Bidard, Frédérique
Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title_full Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title_fullStr Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title_full_unstemmed Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title_short Proximity ligation scaffolding and comparison of two Trichoderma reesei strains genomes
title_sort proximity ligation scaffolding and comparison of two trichoderma reesei strains genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469131/
https://www.ncbi.nlm.nih.gov/pubmed/28616075
http://dx.doi.org/10.1186/s13068-017-0837-6
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