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Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens
BACKGROUND: Many plant-pathogenic fungi have a tendency towards genome size expansion, mostly driven by increasing content of transposable elements (TEs). Through comparative and evolutionary genomics, five members of the Leptosphaeria maculans-Leptosphaeria biglobosa species complex (class Dothideo...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210507/ https://www.ncbi.nlm.nih.gov/pubmed/25306241 http://dx.doi.org/10.1186/1471-2164-15-891 |
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author | Grandaubert, Jonathan Lowe, Rohan GT Soyer, Jessica L Schoch, Conrad L Van de Wouw, Angela P Fudal, Isabelle Robbertse, Barbara Lapalu, Nicolas Links, Matthew G Ollivier, Bénédicte Linglin, Juliette Barbe, Valérie Mangenot, Sophie Cruaud, Corinne Borhan, Hossein Howlett, Barbara J Balesdent, Marie-Hélène Rouxel, Thierry |
author_facet | Grandaubert, Jonathan Lowe, Rohan GT Soyer, Jessica L Schoch, Conrad L Van de Wouw, Angela P Fudal, Isabelle Robbertse, Barbara Lapalu, Nicolas Links, Matthew G Ollivier, Bénédicte Linglin, Juliette Barbe, Valérie Mangenot, Sophie Cruaud, Corinne Borhan, Hossein Howlett, Barbara J Balesdent, Marie-Hélène Rouxel, Thierry |
author_sort | Grandaubert, Jonathan |
collection | PubMed |
description | BACKGROUND: Many plant-pathogenic fungi have a tendency towards genome size expansion, mostly driven by increasing content of transposable elements (TEs). Through comparative and evolutionary genomics, five members of the Leptosphaeria maculans-Leptosphaeria biglobosa species complex (class Dothideomycetes, order Pleosporales), having different host ranges and pathogenic abilities towards cruciferous plants, were studied to infer the role of TEs on genome shaping, speciation, and on the rise of better adapted pathogens. RESULTS: L. maculans ‘brassicae’, the most damaging species on oilseed rape, is the only member of the species complex to have a TE-invaded genome (32.5%) compared to the other members genomes (<4%). These TEs had an impact at the structural level by creating large TE-rich regions and are suspected to have been instrumental in chromosomal rearrangements possibly leading to speciation. TEs, associated with species-specific genes involved in disease process, also possibly had an incidence on evolution of pathogenicity by promoting translocations of effector genes to highly dynamic regions and thus tuning the regulation of effector gene expression in planta. CONCLUSIONS: Invasion of L. maculans ‘brassicae’ genome by TEs followed by bursts of TE activity allowed this species to evolve and to better adapt to its host, making this genome species a peculiarity within its own species complex as well as in the Pleosporales lineage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-891) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4210507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42105072014-10-29 Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens Grandaubert, Jonathan Lowe, Rohan GT Soyer, Jessica L Schoch, Conrad L Van de Wouw, Angela P Fudal, Isabelle Robbertse, Barbara Lapalu, Nicolas Links, Matthew G Ollivier, Bénédicte Linglin, Juliette Barbe, Valérie Mangenot, Sophie Cruaud, Corinne Borhan, Hossein Howlett, Barbara J Balesdent, Marie-Hélène Rouxel, Thierry BMC Genomics Research Article BACKGROUND: Many plant-pathogenic fungi have a tendency towards genome size expansion, mostly driven by increasing content of transposable elements (TEs). Through comparative and evolutionary genomics, five members of the Leptosphaeria maculans-Leptosphaeria biglobosa species complex (class Dothideomycetes, order Pleosporales), having different host ranges and pathogenic abilities towards cruciferous plants, were studied to infer the role of TEs on genome shaping, speciation, and on the rise of better adapted pathogens. RESULTS: L. maculans ‘brassicae’, the most damaging species on oilseed rape, is the only member of the species complex to have a TE-invaded genome (32.5%) compared to the other members genomes (<4%). These TEs had an impact at the structural level by creating large TE-rich regions and are suspected to have been instrumental in chromosomal rearrangements possibly leading to speciation. TEs, associated with species-specific genes involved in disease process, also possibly had an incidence on evolution of pathogenicity by promoting translocations of effector genes to highly dynamic regions and thus tuning the regulation of effector gene expression in planta. CONCLUSIONS: Invasion of L. maculans ‘brassicae’ genome by TEs followed by bursts of TE activity allowed this species to evolve and to better adapt to its host, making this genome species a peculiarity within its own species complex as well as in the Pleosporales lineage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-891) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-12 /pmc/articles/PMC4210507/ /pubmed/25306241 http://dx.doi.org/10.1186/1471-2164-15-891 Text en © Grandaubert et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article Grandaubert, Jonathan Lowe, Rohan GT Soyer, Jessica L Schoch, Conrad L Van de Wouw, Angela P Fudal, Isabelle Robbertse, Barbara Lapalu, Nicolas Links, Matthew G Ollivier, Bénédicte Linglin, Juliette Barbe, Valérie Mangenot, Sophie Cruaud, Corinne Borhan, Hossein Howlett, Barbara J Balesdent, Marie-Hélène Rouxel, Thierry Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title | Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title_full | Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title_fullStr | Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title_full_unstemmed | Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title_short | Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens |
title_sort | transposable element-assisted evolution and adaptation to host plant within the leptosphaeria maculans-leptosphaeria biglobosa species complex of fungal pathogens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210507/ https://www.ncbi.nlm.nih.gov/pubmed/25306241 http://dx.doi.org/10.1186/1471-2164-15-891 |
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