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Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita

In model organisms, epigenome dynamics underlies a plethora of biological processes. The role of epigenetic modifications in development and parasitism in nematode pests remains unknown. The root-knot nematode Meloidogyne incognita adapts rapidly to unfavorable conditions, despite its asexual reprod...

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Autores principales: Hassanaly-Goulamhoussen, Rahim, De Carvalho Augusto, Ronaldo, Marteu-Garello, Nathalie, Péré, Arthur, Favery, Bruno, Da Rocha, Martine, Danchin, Etienne G. J., Abad, Pierre, Grunau, Christoph, Perfus-Barbeoch, Laetitia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685519/
https://www.ncbi.nlm.nih.gov/pubmed/34938734
http://dx.doi.org/10.3389/fcell.2021.765690
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author Hassanaly-Goulamhoussen, Rahim
De Carvalho Augusto, Ronaldo
Marteu-Garello, Nathalie
Péré, Arthur
Favery, Bruno
Da Rocha, Martine
Danchin, Etienne G. J.
Abad, Pierre
Grunau, Christoph
Perfus-Barbeoch, Laetitia
author_facet Hassanaly-Goulamhoussen, Rahim
De Carvalho Augusto, Ronaldo
Marteu-Garello, Nathalie
Péré, Arthur
Favery, Bruno
Da Rocha, Martine
Danchin, Etienne G. J.
Abad, Pierre
Grunau, Christoph
Perfus-Barbeoch, Laetitia
author_sort Hassanaly-Goulamhoussen, Rahim
collection PubMed
description In model organisms, epigenome dynamics underlies a plethora of biological processes. The role of epigenetic modifications in development and parasitism in nematode pests remains unknown. The root-knot nematode Meloidogyne incognita adapts rapidly to unfavorable conditions, despite its asexual reproduction. However, the mechanisms underlying this remarkable plasticity and their potential impact on gene expression remain unknown. This study provides the first insight into contribution of epigenetic mechanisms to this plasticity, by studying histone modifications in M. incognita. The distribution of five histone modifications revealed the existence of strong epigenetic signatures, similar to those found in the model nematode Caenorhabditis elegans. We investigated their impact on chromatin structure and their distribution relative to transposable elements (TE) loci. We assessed the influence of the chromatin landscape on gene expression at two developmental stages: eggs, and pre-parasitic juveniles. H3K4me3 histone modification was strongly correlated with high levels of expression for protein-coding genes implicated in stage-specific processes during M. incognita development. We provided new insights in the dynamic regulation of parasitism genes kept under histone modifications silencing. In this pioneering study, we establish a comprehensive framework for the importance of epigenetic mechanisms in the regulation of the genome expression and its stability in plant-parasitic nematodes.
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spelling pubmed-86855192021-12-21 Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita Hassanaly-Goulamhoussen, Rahim De Carvalho Augusto, Ronaldo Marteu-Garello, Nathalie Péré, Arthur Favery, Bruno Da Rocha, Martine Danchin, Etienne G. J. Abad, Pierre Grunau, Christoph Perfus-Barbeoch, Laetitia Front Cell Dev Biol Cell and Developmental Biology In model organisms, epigenome dynamics underlies a plethora of biological processes. The role of epigenetic modifications in development and parasitism in nematode pests remains unknown. The root-knot nematode Meloidogyne incognita adapts rapidly to unfavorable conditions, despite its asexual reproduction. However, the mechanisms underlying this remarkable plasticity and their potential impact on gene expression remain unknown. This study provides the first insight into contribution of epigenetic mechanisms to this plasticity, by studying histone modifications in M. incognita. The distribution of five histone modifications revealed the existence of strong epigenetic signatures, similar to those found in the model nematode Caenorhabditis elegans. We investigated their impact on chromatin structure and their distribution relative to transposable elements (TE) loci. We assessed the influence of the chromatin landscape on gene expression at two developmental stages: eggs, and pre-parasitic juveniles. H3K4me3 histone modification was strongly correlated with high levels of expression for protein-coding genes implicated in stage-specific processes during M. incognita development. We provided new insights in the dynamic regulation of parasitism genes kept under histone modifications silencing. In this pioneering study, we establish a comprehensive framework for the importance of epigenetic mechanisms in the regulation of the genome expression and its stability in plant-parasitic nematodes. Frontiers Media S.A. 2021-12-06 /pmc/articles/PMC8685519/ /pubmed/34938734 http://dx.doi.org/10.3389/fcell.2021.765690 Text en Copyright © 2021 Hassanaly-Goulamhoussen, De Carvalho Augusto, Marteu-Garello, Péré, Favery, Da Rocha, Danchin, Abad, Grunau and Perfus-Barbeoch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Hassanaly-Goulamhoussen, Rahim
De Carvalho Augusto, Ronaldo
Marteu-Garello, Nathalie
Péré, Arthur
Favery, Bruno
Da Rocha, Martine
Danchin, Etienne G. J.
Abad, Pierre
Grunau, Christoph
Perfus-Barbeoch, Laetitia
Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title_full Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title_fullStr Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title_full_unstemmed Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title_short Chromatin Landscape Dynamics in the Early Development of the Plant Parasitic Nematode Meloidogyne incognita
title_sort chromatin landscape dynamics in the early development of the plant parasitic nematode meloidogyne incognita
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685519/
https://www.ncbi.nlm.nih.gov/pubmed/34938734
http://dx.doi.org/10.3389/fcell.2021.765690
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