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The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice
Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832823/ https://www.ncbi.nlm.nih.gov/pubmed/29497084 http://dx.doi.org/10.1038/s41598-018-22101-6 |
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author | Filipe, Osvaldo De Vleesschauwer, David Haeck, Ashley Demeestere, Kristof Höfte, Monica |
author_facet | Filipe, Osvaldo De Vleesschauwer, David Haeck, Ashley Demeestere, Kristof Höfte, Monica |
author_sort | Filipe, Osvaldo |
collection | PubMed |
description | Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate the required adaptations to maintain energy homeostasis and survival. In plants, SnRK1 is a global regulator of plant metabolism and is also involved in abiotic stress responses. Its role in the response to biotic stress, however, is only starting to be uncovered. Here we studied the effect of altered SnRK1a expression on growth and plant defense in rice. OsSnRK1a overexpression interfered with normal growth and development and increased resistance against both (hemi)biotrophic and necrotrophic pathogens, while OsSnRK1a silencing in RNAi lines increased susceptibility. OsSnRK1a overexpression positively affected the salicylic acid pathway and boosted the jasmonate-mediated defense response after inoculation with the blast fungus Pyricularia oryzae. Together these findings strongly suggest OsSnRK1a to be involved in plant basal immunity and favor a model whereby OsSnRK1a acts as a master switch that regulates growth-immunity trade-offs. |
format | Online Article Text |
id | pubmed-5832823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58328232018-03-05 The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice Filipe, Osvaldo De Vleesschauwer, David Haeck, Ashley Demeestere, Kristof Höfte, Monica Sci Rep Article Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) belongs to a family of evolutionary conserved kinases with orthologs in all eukaryotes, ranging from yeasts (SnF1) to mammals (AMP-Activated kinase). These kinases sense energy deficits caused by nutrient limitation or stress and coordinate the required adaptations to maintain energy homeostasis and survival. In plants, SnRK1 is a global regulator of plant metabolism and is also involved in abiotic stress responses. Its role in the response to biotic stress, however, is only starting to be uncovered. Here we studied the effect of altered SnRK1a expression on growth and plant defense in rice. OsSnRK1a overexpression interfered with normal growth and development and increased resistance against both (hemi)biotrophic and necrotrophic pathogens, while OsSnRK1a silencing in RNAi lines increased susceptibility. OsSnRK1a overexpression positively affected the salicylic acid pathway and boosted the jasmonate-mediated defense response after inoculation with the blast fungus Pyricularia oryzae. Together these findings strongly suggest OsSnRK1a to be involved in plant basal immunity and favor a model whereby OsSnRK1a acts as a master switch that regulates growth-immunity trade-offs. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5832823/ /pubmed/29497084 http://dx.doi.org/10.1038/s41598-018-22101-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Filipe, Osvaldo De Vleesschauwer, David Haeck, Ashley Demeestere, Kristof Höfte, Monica The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title | The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title_full | The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title_fullStr | The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title_full_unstemmed | The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title_short | The energy sensor OsSnRK1a confers broad-spectrum disease resistance in rice |
title_sort | energy sensor ossnrk1a confers broad-spectrum disease resistance in rice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832823/ https://www.ncbi.nlm.nih.gov/pubmed/29497084 http://dx.doi.org/10.1038/s41598-018-22101-6 |
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