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Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus
BACKGROUND: Cochliobolus heterostrophus is a dothideomycete that causes Southern Corn Leaf Blight disease. There are two races, race O and race T that differ by the absence (race O) and presence (race T) of ~ 1.2-Mb of DNA encoding genes responsible for the production of T-toxin, which makes race T...
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/PMC4112212/ https://www.ncbi.nlm.nih.gov/pubmed/24973942 http://dx.doi.org/10.1186/1471-2164-15-536 |
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author | Santana, Mateus F Silva, José CF Mizubuti, Eduardo SG Araújo, Elza F Condon, Bradford J Turgeon, B Gillian Queiroz, Marisa V |
author_facet | Santana, Mateus F Silva, José CF Mizubuti, Eduardo SG Araújo, Elza F Condon, Bradford J Turgeon, B Gillian Queiroz, Marisa V |
author_sort | Santana, Mateus F |
collection | PubMed |
description | BACKGROUND: Cochliobolus heterostrophus is a dothideomycete that causes Southern Corn Leaf Blight disease. There are two races, race O and race T that differ by the absence (race O) and presence (race T) of ~ 1.2-Mb of DNA encoding genes responsible for the production of T-toxin, which makes race T much more virulent than race O. The presence of repetitive elements in fungal genomes is considered to be an important source of genetic variability between different species. RESULTS: A detailed analysis of class I and II TEs identified in the near complete genome sequence of race O was performed. In total in race O, 12 new families of transposons were identified. In silico evidence of recent activity was found for many of the transposons and analyses of expressed sequence tags (ESTs) demonstrated that these elements were actively transcribed. Various potentially active TEs were found near coding regions and may modify the expression and structure of these genes by acting as ectopic recombination sites. Transposons were found on scaffolds carrying polyketide synthase encoding genes, responsible for production of T-toxin in race T. Strong evidence of ectopic recombination was found, demonstrating that TEs can play an important role in the modulation of genome architecture of this species. The Repeat Induced Point mutation (RIP) silencing mechanism was shown to have high specificity in C. heterostrophus, acting only on transposons near coding regions. CONCLUSIONS: New families of transposons were identified. In C. heterostrophus, the RIP silencing mechanism is efficient and selective. The co-localization of effector genes and TEs, therefore, exposes those genes to high rates of point mutations. This may accelerate the rate of evolution of these genes, providing a potential advantage for the host. Additionally, it was shown that ectopic recombination promoted by TEs appears to be the major event in the genome reorganization of this species and that a large number of elements are still potentially active. So, this study provides information about the potential impact of TEs on the evolution of C. heterostrophus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-536) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4112212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41122122014-08-05 Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus Santana, Mateus F Silva, José CF Mizubuti, Eduardo SG Araújo, Elza F Condon, Bradford J Turgeon, B Gillian Queiroz, Marisa V BMC Genomics Research Article BACKGROUND: Cochliobolus heterostrophus is a dothideomycete that causes Southern Corn Leaf Blight disease. There are two races, race O and race T that differ by the absence (race O) and presence (race T) of ~ 1.2-Mb of DNA encoding genes responsible for the production of T-toxin, which makes race T much more virulent than race O. The presence of repetitive elements in fungal genomes is considered to be an important source of genetic variability between different species. RESULTS: A detailed analysis of class I and II TEs identified in the near complete genome sequence of race O was performed. In total in race O, 12 new families of transposons were identified. In silico evidence of recent activity was found for many of the transposons and analyses of expressed sequence tags (ESTs) demonstrated that these elements were actively transcribed. Various potentially active TEs were found near coding regions and may modify the expression and structure of these genes by acting as ectopic recombination sites. Transposons were found on scaffolds carrying polyketide synthase encoding genes, responsible for production of T-toxin in race T. Strong evidence of ectopic recombination was found, demonstrating that TEs can play an important role in the modulation of genome architecture of this species. The Repeat Induced Point mutation (RIP) silencing mechanism was shown to have high specificity in C. heterostrophus, acting only on transposons near coding regions. CONCLUSIONS: New families of transposons were identified. In C. heterostrophus, the RIP silencing mechanism is efficient and selective. The co-localization of effector genes and TEs, therefore, exposes those genes to high rates of point mutations. This may accelerate the rate of evolution of these genes, providing a potential advantage for the host. Additionally, it was shown that ectopic recombination promoted by TEs appears to be the major event in the genome reorganization of this species and that a large number of elements are still potentially active. So, this study provides information about the potential impact of TEs on the evolution of C. heterostrophus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-536) contains supplementary material, which is available to authorized users. BioMed Central 2014-06-28 /pmc/articles/PMC4112212/ /pubmed/24973942 http://dx.doi.org/10.1186/1471-2164-15-536 Text en © Santana 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 Santana, Mateus F Silva, José CF Mizubuti, Eduardo SG Araújo, Elza F Condon, Bradford J Turgeon, B Gillian Queiroz, Marisa V Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title_full | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title_fullStr | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title_full_unstemmed | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title_short | Characterization and potential evolutionary impact of transposable elements in the genome of Cochliobolus heterostrophus |
title_sort | characterization and potential evolutionary impact of transposable elements in the genome of cochliobolus heterostrophus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112212/ https://www.ncbi.nlm.nih.gov/pubmed/24973942 http://dx.doi.org/10.1186/1471-2164-15-536 |
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