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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...

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Autores principales: Soto-Suárez, Mauricio, Baldrich, Patricia, Weigel, Detlef, Rubio-Somoza, Ignacio, San Segundo, Blanca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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