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Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen

Effector proteins are secreted by plant pathogens to enable host colonization. Typically, effector genes are tightly regulated, have very low expression levels in axenic conditions, and are strongly induced during host colonization. Chromatin remodeling contributes to the activation of effector gene...

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Autores principales: Suarez-Fernandez, Marta, Álvarez-Aragón, Rocio, Pastor-Mediavilla, Ana, Maestre-Guillén, Alejandro, del Olmo, Ivan, De Francesco, Agustina, Meile, Lukas, Sánchez-Vallet, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653901/
https://www.ncbi.nlm.nih.gov/pubmed/37642412
http://dx.doi.org/10.1128/mbio.01386-23
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author Suarez-Fernandez, Marta
Álvarez-Aragón, Rocio
Pastor-Mediavilla, Ana
Maestre-Guillén, Alejandro
del Olmo, Ivan
De Francesco, Agustina
Meile, Lukas
Sánchez-Vallet, Andrea
author_facet Suarez-Fernandez, Marta
Álvarez-Aragón, Rocio
Pastor-Mediavilla, Ana
Maestre-Guillén, Alejandro
del Olmo, Ivan
De Francesco, Agustina
Meile, Lukas
Sánchez-Vallet, Andrea
author_sort Suarez-Fernandez, Marta
collection PubMed
description Effector proteins are secreted by plant pathogens to enable host colonization. Typically, effector genes are tightly regulated, have very low expression levels in axenic conditions, and are strongly induced during host colonization. Chromatin remodeling contributes to the activation of effector genes in planta by still poorly known mechanisms. In this work, we investigated the role of histone acetylation in effector gene derepression in plant pathogens. We used Zymoseptoria tritici, a major pathogen of wheat, as a model to determine the role of lysine acetyltransferases (KATs) in plant infection. We showed that effector gene activation is associated with chromatin remodeling, featuring increased acetylation levels of histone H3 lysine 9 (H3K9) and 14 (H3K14) in effector loci. We functionally characterized the role of Z. tritici KATs and demonstrated their distinct contributions to growth, development, and infection. Sas3 is required for host colonization and pycnidia production and is involved in the acetylation of H3K9 and H3K14 in effector loci and, consequently, in effector gene activation during plant infection. We propose that Sas3-mediated histone acetylation is required for the spatiotemporal activation of effector genes and the virulence of Z. tritici. IMPORTANCE: Pathogen infections require the production of effectors that enable host colonization. Effectors have diverse functions and are only expressed at certain stages of the infection cycle. Thus, effector genes are tightly regulated by several mechanisms, including chromatin remodeling. Here, we investigate the role of histone acetylation in effector gene activation in the fungal wheat pathogen Zymoseptoria tritici. We demonstrate that lysine acetyltransferases (KATs) are essential for the spatiotemporal regulation of effector genes. We show that the KAT Sas3 is involved in leaf symptom development and pycnidia formation. Importantly, our results indicate that Sas3 controls histone acetylation of effector loci and is a regulator of effector gene activation during stomatal penetration. Overall, our work demonstrates the key role of histone acetylation in regulating gene expression associated with plant infection.
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spelling pubmed-106539012023-08-29 Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen Suarez-Fernandez, Marta Álvarez-Aragón, Rocio Pastor-Mediavilla, Ana Maestre-Guillén, Alejandro del Olmo, Ivan De Francesco, Agustina Meile, Lukas Sánchez-Vallet, Andrea mBio Research Article Effector proteins are secreted by plant pathogens to enable host colonization. Typically, effector genes are tightly regulated, have very low expression levels in axenic conditions, and are strongly induced during host colonization. Chromatin remodeling contributes to the activation of effector genes in planta by still poorly known mechanisms. In this work, we investigated the role of histone acetylation in effector gene derepression in plant pathogens. We used Zymoseptoria tritici, a major pathogen of wheat, as a model to determine the role of lysine acetyltransferases (KATs) in plant infection. We showed that effector gene activation is associated with chromatin remodeling, featuring increased acetylation levels of histone H3 lysine 9 (H3K9) and 14 (H3K14) in effector loci. We functionally characterized the role of Z. tritici KATs and demonstrated their distinct contributions to growth, development, and infection. Sas3 is required for host colonization and pycnidia production and is involved in the acetylation of H3K9 and H3K14 in effector loci and, consequently, in effector gene activation during plant infection. We propose that Sas3-mediated histone acetylation is required for the spatiotemporal activation of effector genes and the virulence of Z. tritici. IMPORTANCE: Pathogen infections require the production of effectors that enable host colonization. Effectors have diverse functions and are only expressed at certain stages of the infection cycle. Thus, effector genes are tightly regulated by several mechanisms, including chromatin remodeling. Here, we investigate the role of histone acetylation in effector gene activation in the fungal wheat pathogen Zymoseptoria tritici. We demonstrate that lysine acetyltransferases (KATs) are essential for the spatiotemporal regulation of effector genes. We show that the KAT Sas3 is involved in leaf symptom development and pycnidia formation. Importantly, our results indicate that Sas3 controls histone acetylation of effector loci and is a regulator of effector gene activation during stomatal penetration. Overall, our work demonstrates the key role of histone acetylation in regulating gene expression associated with plant infection. American Society for Microbiology 2023-08-29 /pmc/articles/PMC10653901/ /pubmed/37642412 http://dx.doi.org/10.1128/mbio.01386-23 Text en Copyright © 2023 Suarez-Fernandez 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
Suarez-Fernandez, Marta
Álvarez-Aragón, Rocio
Pastor-Mediavilla, Ana
Maestre-Guillén, Alejandro
del Olmo, Ivan
De Francesco, Agustina
Meile, Lukas
Sánchez-Vallet, Andrea
Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title_full Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title_fullStr Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title_full_unstemmed Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title_short Sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
title_sort sas3-mediated histone acetylation regulates effector gene activation in a fungal plant pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653901/
https://www.ncbi.nlm.nih.gov/pubmed/37642412
http://dx.doi.org/10.1128/mbio.01386-23
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