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Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen

Dynamic changes in transcription profiles are key for the success of pathogens in colonizing their hosts. In many pathogens, genes associated with virulence, such as effector genes, are located in regions of the genome that are rich in transposable elements and heterochromatin. The contribution of c...

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Autores principales: Meile, Lukas, Peter, Jules, Puccetti, Guido, Alassimone, Julien, McDonald, Bruce A., Sánchez-Vallet, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542367/
https://www.ncbi.nlm.nih.gov/pubmed/33024042
http://dx.doi.org/10.1128/mBio.02343-20
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author Meile, Lukas
Peter, Jules
Puccetti, Guido
Alassimone, Julien
McDonald, Bruce A.
Sánchez-Vallet, Andrea
author_facet Meile, Lukas
Peter, Jules
Puccetti, Guido
Alassimone, Julien
McDonald, Bruce A.
Sánchez-Vallet, Andrea
author_sort Meile, Lukas
collection PubMed
description Dynamic changes in transcription profiles are key for the success of pathogens in colonizing their hosts. In many pathogens, genes associated with virulence, such as effector genes, are located in regions of the genome that are rich in transposable elements and heterochromatin. The contribution of chromatin modifications to gene expression in pathogens remains largely unknown. Using a combination of a reporter gene-based approach and chromatin immunoprecipitation, we show that the heterochromatic environment of effector genes in the fungal plant pathogen Zymoseptoria tritici is a key regulator of their specific spatiotemporal expression patterns. Enrichment in trimethylated lysine 27 of histone H3 dictates the repression of effector genes in the absence of the host. Chromatin decondensation during host colonization, featuring a reduction in this repressive modification, indicates a major role for epigenetics in effector gene induction. Our results illustrate that chromatin modifications triggered during host colonization determine the specific expression profile of effector genes at the cellular level and, hence, provide new insights into the regulation of virulence in fungal plant pathogens.
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spelling pubmed-75423672020-10-19 Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen Meile, Lukas Peter, Jules Puccetti, Guido Alassimone, Julien McDonald, Bruce A. Sánchez-Vallet, Andrea mBio Research Article Dynamic changes in transcription profiles are key for the success of pathogens in colonizing their hosts. In many pathogens, genes associated with virulence, such as effector genes, are located in regions of the genome that are rich in transposable elements and heterochromatin. The contribution of chromatin modifications to gene expression in pathogens remains largely unknown. Using a combination of a reporter gene-based approach and chromatin immunoprecipitation, we show that the heterochromatic environment of effector genes in the fungal plant pathogen Zymoseptoria tritici is a key regulator of their specific spatiotemporal expression patterns. Enrichment in trimethylated lysine 27 of histone H3 dictates the repression of effector genes in the absence of the host. Chromatin decondensation during host colonization, featuring a reduction in this repressive modification, indicates a major role for epigenetics in effector gene induction. Our results illustrate that chromatin modifications triggered during host colonization determine the specific expression profile of effector genes at the cellular level and, hence, provide new insights into the regulation of virulence in fungal plant pathogens. American Society for Microbiology 2020-10-06 /pmc/articles/PMC7542367/ /pubmed/33024042 http://dx.doi.org/10.1128/mBio.02343-20 Text en Copyright © 2020 Meile et al. https://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 (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Meile, Lukas
Peter, Jules
Puccetti, Guido
Alassimone, Julien
McDonald, Bruce A.
Sánchez-Vallet, Andrea
Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title_full Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title_fullStr Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title_full_unstemmed Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title_short Chromatin Dynamics Contribute to the Spatiotemporal Expression Pattern of Virulence Genes in a Fungal Plant Pathogen
title_sort chromatin dynamics contribute to the spatiotemporal expression pattern of virulence genes in a fungal plant pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542367/
https://www.ncbi.nlm.nih.gov/pubmed/33024042
http://dx.doi.org/10.1128/mBio.02343-20
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