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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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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. |
format | Online Article Text |
id | pubmed-10653901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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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