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The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens
MicroRNAs (miRNAs) play a pivotal role in regulating gene expression during plant development. Although a substantial fraction of plant miRNAs has proven responsive to pathogen infection, their role in disease resistance remains largely unknown, especially during fungal infections. In this study, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362962/ https://www.ncbi.nlm.nih.gov/pubmed/28332603 http://dx.doi.org/10.1038/srep44898 |
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author | Soto-Suárez, Mauricio Baldrich, Patricia Weigel, Detlef Rubio-Somoza, Ignacio San Segundo, Blanca |
author_facet | Soto-Suárez, Mauricio Baldrich, Patricia Weigel, Detlef Rubio-Somoza, Ignacio San Segundo, Blanca |
author_sort | Soto-Suárez, Mauricio |
collection | PubMed |
description | MicroRNAs (miRNAs) play a pivotal role in regulating gene expression during plant development. Although a substantial fraction of plant miRNAs has proven responsive to pathogen infection, their role in disease resistance remains largely unknown, especially during fungal infections. In this study, we screened Arabidopsis thaliana lines in which miRNA activity has been reduced using artificial miRNA target mimics (MIM lines) for their response to fungal pathogens. Reduced activity of miR396 (MIM396 plants) was found to confer broad resistance to necrotrophic and hemibiotrophic fungal pathogens. MiR396 levels gradually decreased during fungal infection, thus, enabling its GRF (GROWTH-REGULATING FACTOR) transcription factor target genes to trigger host reprogramming. Pathogen resistance in MIM396 plants is based on a superactivation of defense responses consistent with a priming event during pathogen infection. Notably, low levels of miR396 are not translated in developmental defects in absence of pathogen challenge. Our findings support a role of miR396 in regulating plant immunity, and broaden our knowledge about the molecular players and processes that sustain defense priming. That miR396 modulates innate immunity without growth costs also suggests fine-tuning of miR396 levels as an effective biotechnological means for protection against pathogen infection. |
format | Online Article Text |
id | pubmed-5362962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53629622017-03-24 The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens Soto-Suárez, Mauricio Baldrich, Patricia Weigel, Detlef Rubio-Somoza, Ignacio San Segundo, Blanca Sci Rep Article MicroRNAs (miRNAs) play a pivotal role in regulating gene expression during plant development. Although a substantial fraction of plant miRNAs has proven responsive to pathogen infection, their role in disease resistance remains largely unknown, especially during fungal infections. In this study, we screened Arabidopsis thaliana lines in which miRNA activity has been reduced using artificial miRNA target mimics (MIM lines) for their response to fungal pathogens. Reduced activity of miR396 (MIM396 plants) was found to confer broad resistance to necrotrophic and hemibiotrophic fungal pathogens. MiR396 levels gradually decreased during fungal infection, thus, enabling its GRF (GROWTH-REGULATING FACTOR) transcription factor target genes to trigger host reprogramming. Pathogen resistance in MIM396 plants is based on a superactivation of defense responses consistent with a priming event during pathogen infection. Notably, low levels of miR396 are not translated in developmental defects in absence of pathogen challenge. Our findings support a role of miR396 in regulating plant immunity, and broaden our knowledge about the molecular players and processes that sustain defense priming. That miR396 modulates innate immunity without growth costs also suggests fine-tuning of miR396 levels as an effective biotechnological means for protection against pathogen infection. Nature Publishing Group 2017-03-23 /pmc/articles/PMC5362962/ /pubmed/28332603 http://dx.doi.org/10.1038/srep44898 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Soto-Suárez, Mauricio Baldrich, Patricia Weigel, Detlef Rubio-Somoza, Ignacio San Segundo, Blanca The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title | The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title_full | The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title_fullStr | The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title_full_unstemmed | The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title_short | The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
title_sort | arabidopsis mir396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362962/ https://www.ncbi.nlm.nih.gov/pubmed/28332603 http://dx.doi.org/10.1038/srep44898 |
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