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Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola

Epigenetic processes play a crucial role in the regulation of plant stress responses, but their role in plant–pathogen interactions remains poorly understood. Although histone‐modifying enzymes have been observed to be deregulated in galls induced by root‐knot nematodes (RKN, Meloidogyne graminicola...

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Autores principales: Atighi, Mohammad Reza, Verstraeten, Bruno, De Meyer, Tim, Kyndt, Tina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938626/
https://www.ncbi.nlm.nih.gov/pubmed/33580630
http://dx.doi.org/10.1111/mpp.13037
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author Atighi, Mohammad Reza
Verstraeten, Bruno
De Meyer, Tim
Kyndt, Tina
author_facet Atighi, Mohammad Reza
Verstraeten, Bruno
De Meyer, Tim
Kyndt, Tina
author_sort Atighi, Mohammad Reza
collection PubMed
description Epigenetic processes play a crucial role in the regulation of plant stress responses, but their role in plant–pathogen interactions remains poorly understood. Although histone‐modifying enzymes have been observed to be deregulated in galls induced by root‐knot nematodes (RKN, Meloidogyne graminicola) in rice, their influence on plant defence and their genome‐wide impact has not been comprehensively investigated. First, the role of histone modifications in plant–nematode interactions was confirmed by pharmacological inhibition of histone‐modifying enzymes, which all significantly affected rice susceptibility to RKN. For a more specific view, three histone marks, H3K9ac, H3K9me2, and H3K27me3, were subsequently studied by chromatin‐immunoprecipitation‐sequencing on RKN‐induced galls at 3 days postinoculation. While levels of H3K9ac and H3K27me3 were strongly enriched, H3K9me2 was generally depleted in galls versus control root tips. Differential histone peaks were generally associated with plant defence‐related genes. Transcriptome analysis using RNA‐Seq and RT‐qPCR‐based validation revealed that genes marked with H3K9ac or H3K9me2 showed the expected activation or repression gene expression pattern, but this was not the case for H3K27me3 marks. Our results indicate that histone modifications respond dynamically to RKN infection, and that posttranslational modifications mainly at H3K9 specifically target plant defence‐related genes.
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spelling pubmed-79386262021-03-16 Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola Atighi, Mohammad Reza Verstraeten, Bruno De Meyer, Tim Kyndt, Tina Mol Plant Pathol Original Articles Epigenetic processes play a crucial role in the regulation of plant stress responses, but their role in plant–pathogen interactions remains poorly understood. Although histone‐modifying enzymes have been observed to be deregulated in galls induced by root‐knot nematodes (RKN, Meloidogyne graminicola) in rice, their influence on plant defence and their genome‐wide impact has not been comprehensively investigated. First, the role of histone modifications in plant–nematode interactions was confirmed by pharmacological inhibition of histone‐modifying enzymes, which all significantly affected rice susceptibility to RKN. For a more specific view, three histone marks, H3K9ac, H3K9me2, and H3K27me3, were subsequently studied by chromatin‐immunoprecipitation‐sequencing on RKN‐induced galls at 3 days postinoculation. While levels of H3K9ac and H3K27me3 were strongly enriched, H3K9me2 was generally depleted in galls versus control root tips. Differential histone peaks were generally associated with plant defence‐related genes. Transcriptome analysis using RNA‐Seq and RT‐qPCR‐based validation revealed that genes marked with H3K9ac or H3K9me2 showed the expected activation or repression gene expression pattern, but this was not the case for H3K27me3 marks. Our results indicate that histone modifications respond dynamically to RKN infection, and that posttranslational modifications mainly at H3K9 specifically target plant defence‐related genes. John Wiley and Sons Inc. 2021-02-12 /pmc/articles/PMC7938626/ /pubmed/33580630 http://dx.doi.org/10.1111/mpp.13037 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Atighi, Mohammad Reza
Verstraeten, Bruno
De Meyer, Tim
Kyndt, Tina
Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title_full Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title_fullStr Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title_full_unstemmed Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title_short Genome‐wide shifts in histone modifications at early stage of rice infection with Meloidogyne graminicola
title_sort genome‐wide shifts in histone modifications at early stage of rice infection with meloidogyne graminicola
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938626/
https://www.ncbi.nlm.nih.gov/pubmed/33580630
http://dx.doi.org/10.1111/mpp.13037
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