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Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes

Root-knot nematodes (genus Meloidogyne) are the major contributor to crop losses caused by nematodes. These nematodes secrete effector proteins into the plant, derived from two sets of pharyngeal gland cells, to manipulate host physiology and immunity. Successful completion of the life cycle, involv...

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Autores principales: Da Rocha, Martine, Bournaud, Caroline, Dazenière, Julie, Thorpe, Peter, Bailly-Bechet, Marc, Pellegrin, Clément, Péré, Arthur, Grynberg, Priscila, Perfus-Barbeoch, Laetitia, Eves-van den Akker, Sebastian, Danchin, Etienne G. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158474/
https://www.ncbi.nlm.nih.gov/pubmed/34070210
http://dx.doi.org/10.3390/genes12050771
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author Da Rocha, Martine
Bournaud, Caroline
Dazenière, Julie
Thorpe, Peter
Bailly-Bechet, Marc
Pellegrin, Clément
Péré, Arthur
Grynberg, Priscila
Perfus-Barbeoch, Laetitia
Eves-van den Akker, Sebastian
Danchin, Etienne G. J.
author_facet Da Rocha, Martine
Bournaud, Caroline
Dazenière, Julie
Thorpe, Peter
Bailly-Bechet, Marc
Pellegrin, Clément
Péré, Arthur
Grynberg, Priscila
Perfus-Barbeoch, Laetitia
Eves-van den Akker, Sebastian
Danchin, Etienne G. J.
author_sort Da Rocha, Martine
collection PubMed
description Root-knot nematodes (genus Meloidogyne) are the major contributor to crop losses caused by nematodes. These nematodes secrete effector proteins into the plant, derived from two sets of pharyngeal gland cells, to manipulate host physiology and immunity. Successful completion of the life cycle, involving successive molts from egg to adult, covers morphologically and functionally distinct stages and will require precise control of gene expression, including effector genes. The details of how root-knot nematodes regulate transcription remain sparse. Here, we report a life stage-specific transcriptome of Meloidogyne incognita. Combined with an available annotated genome, we explore the spatio-temporal regulation of gene expression. We reveal gene expression clusters and predicted functions that accompany the major developmental transitions. Focusing on effectors, we identify a putative cis-regulatory motif associated with expression in the dorsal glands, providing an insight into effector regulation. We combine the presence of this motif with several other criteria to predict a novel set of putative dorsal gland effectors. Finally, we show this motif, and thereby its utility, is broadly conserved across the Meloidogyne genus, and we name it Mel-DOG. Taken together, we provide the first genome-wide analysis of spatio-temporal gene expression in a root-knot nematode and identify a new set of candidate effector genes that will guide future functional analyses.
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spelling pubmed-81584742021-05-28 Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes Da Rocha, Martine Bournaud, Caroline Dazenière, Julie Thorpe, Peter Bailly-Bechet, Marc Pellegrin, Clément Péré, Arthur Grynberg, Priscila Perfus-Barbeoch, Laetitia Eves-van den Akker, Sebastian Danchin, Etienne G. J. Genes (Basel) Article Root-knot nematodes (genus Meloidogyne) are the major contributor to crop losses caused by nematodes. These nematodes secrete effector proteins into the plant, derived from two sets of pharyngeal gland cells, to manipulate host physiology and immunity. Successful completion of the life cycle, involving successive molts from egg to adult, covers morphologically and functionally distinct stages and will require precise control of gene expression, including effector genes. The details of how root-knot nematodes regulate transcription remain sparse. Here, we report a life stage-specific transcriptome of Meloidogyne incognita. Combined with an available annotated genome, we explore the spatio-temporal regulation of gene expression. We reveal gene expression clusters and predicted functions that accompany the major developmental transitions. Focusing on effectors, we identify a putative cis-regulatory motif associated with expression in the dorsal glands, providing an insight into effector regulation. We combine the presence of this motif with several other criteria to predict a novel set of putative dorsal gland effectors. Finally, we show this motif, and thereby its utility, is broadly conserved across the Meloidogyne genus, and we name it Mel-DOG. Taken together, we provide the first genome-wide analysis of spatio-temporal gene expression in a root-knot nematode and identify a new set of candidate effector genes that will guide future functional analyses. MDPI 2021-05-18 /pmc/articles/PMC8158474/ /pubmed/34070210 http://dx.doi.org/10.3390/genes12050771 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Da Rocha, Martine
Bournaud, Caroline
Dazenière, Julie
Thorpe, Peter
Bailly-Bechet, Marc
Pellegrin, Clément
Péré, Arthur
Grynberg, Priscila
Perfus-Barbeoch, Laetitia
Eves-van den Akker, Sebastian
Danchin, Etienne G. J.
Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title_full Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title_fullStr Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title_full_unstemmed Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title_short Genome Expression Dynamics Reveal the Parasitism Regulatory Landscape of the Root-Knot Nematode Meloidogyne incognita and a Promoter Motif Associated with Effector Genes
title_sort genome expression dynamics reveal the parasitism regulatory landscape of the root-knot nematode meloidogyne incognita and a promoter motif associated with effector genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158474/
https://www.ncbi.nlm.nih.gov/pubmed/34070210
http://dx.doi.org/10.3390/genes12050771
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