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A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization
Arguably, symbiotic arbuscular mycorrhizal (AM) fungi have the broadest host range of all fungi, being able to intracellularly colonise root cells in the vast majority of all land plants. This raises the question how AM fungi effectively deal with the immune systems of such a widely diverse range of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048545/ https://www.ncbi.nlm.nih.gov/pubmed/33507543 http://dx.doi.org/10.1111/nph.17236 |
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author | Wang, Peng Jiang, Henan Boeren, Sjef Dings, Harm Kulikova, Olga Bisseling, Ton Limpens, Erik |
author_facet | Wang, Peng Jiang, Henan Boeren, Sjef Dings, Harm Kulikova, Olga Bisseling, Ton Limpens, Erik |
author_sort | Wang, Peng |
collection | PubMed |
description | Arguably, symbiotic arbuscular mycorrhizal (AM) fungi have the broadest host range of all fungi, being able to intracellularly colonise root cells in the vast majority of all land plants. This raises the question how AM fungi effectively deal with the immune systems of such a widely diverse range of plants. Here, we studied the role of a nuclear‐localisation signal‐containing effector from Rhizophagus irregularis, called Nuclear Localised Effector1 (RiNLE1), that is highly and specifically expressed in arbuscules. We showed that RiNLE1 is able to translocate to the host nucleus where it interacts with the plant core nucleosome protein histone 2B (H2B). RiNLE1 is able to impair the mono‐ubiquitination of H2B, which results in the suppression of defence‐related gene expression and enhanced colonisation levels. This study highlights a novel mechanism by which AM fungi can effectively control plant epigenetic modifications through direct interaction with a core nucleosome component. Homologues of RiNLE1 are found in a range of fungi that establish intimate interactions with plants, suggesting that this type of effector may be more widely recruited to manipulate host defence responses. |
format | Online Article Text |
id | pubmed-8048545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80485452021-04-19 A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization Wang, Peng Jiang, Henan Boeren, Sjef Dings, Harm Kulikova, Olga Bisseling, Ton Limpens, Erik New Phytol Research Arguably, symbiotic arbuscular mycorrhizal (AM) fungi have the broadest host range of all fungi, being able to intracellularly colonise root cells in the vast majority of all land plants. This raises the question how AM fungi effectively deal with the immune systems of such a widely diverse range of plants. Here, we studied the role of a nuclear‐localisation signal‐containing effector from Rhizophagus irregularis, called Nuclear Localised Effector1 (RiNLE1), that is highly and specifically expressed in arbuscules. We showed that RiNLE1 is able to translocate to the host nucleus where it interacts with the plant core nucleosome protein histone 2B (H2B). RiNLE1 is able to impair the mono‐ubiquitination of H2B, which results in the suppression of defence‐related gene expression and enhanced colonisation levels. This study highlights a novel mechanism by which AM fungi can effectively control plant epigenetic modifications through direct interaction with a core nucleosome component. Homologues of RiNLE1 are found in a range of fungi that establish intimate interactions with plants, suggesting that this type of effector may be more widely recruited to manipulate host defence responses. John Wiley and Sons Inc. 2021-02-28 2021-05 /pmc/articles/PMC8048545/ /pubmed/33507543 http://dx.doi.org/10.1111/nph.17236 Text en © 2021 The Authors New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 | Research Wang, Peng Jiang, Henan Boeren, Sjef Dings, Harm Kulikova, Olga Bisseling, Ton Limpens, Erik A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title | A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title_full | A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title_fullStr | A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title_full_unstemmed | A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title_short | A nuclear‐targeted effector of Rhizophagus irregularis interferes with histone 2B mono‐ubiquitination to promote arbuscular mycorrhization |
title_sort | nuclear‐targeted effector of rhizophagus irregularis interferes with histone 2b mono‐ubiquitination to promote arbuscular mycorrhization |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048545/ https://www.ncbi.nlm.nih.gov/pubmed/33507543 http://dx.doi.org/10.1111/nph.17236 |
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