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Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum

Nitrogen (N) is one of the main limiting nutrients for plant growth and crop yield. It is well documented that changes in nitrate availability, the main N source found in agricultural soils, influences a myriad of developmental programs and processes including the plant defense response. Indeed, man...

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Autores principales: Vega, Andrea, Canessa, Paulo, Hoppe, Gustavo, Retamal, Ignacio, Moyano, Tomas C., Canales, Javier, Gutiérrez, Rodrigo A., Rubilar, Joselyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631835/
https://www.ncbi.nlm.nih.gov/pubmed/26583019
http://dx.doi.org/10.3389/fpls.2015.00911
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author Vega, Andrea
Canessa, Paulo
Hoppe, Gustavo
Retamal, Ignacio
Moyano, Tomas C.
Canales, Javier
Gutiérrez, Rodrigo A.
Rubilar, Joselyn
author_facet Vega, Andrea
Canessa, Paulo
Hoppe, Gustavo
Retamal, Ignacio
Moyano, Tomas C.
Canales, Javier
Gutiérrez, Rodrigo A.
Rubilar, Joselyn
author_sort Vega, Andrea
collection PubMed
description Nitrogen (N) is one of the main limiting nutrients for plant growth and crop yield. It is well documented that changes in nitrate availability, the main N source found in agricultural soils, influences a myriad of developmental programs and processes including the plant defense response. Indeed, many agronomical reports indicate that the plant N nutritional status influences their ability to respond effectively when challenged by different pathogens. However, the molecular mechanisms involved in N-modulation of plant susceptibility to pathogens are poorly characterized. In this work, we show that Solanum lycopersicum defense response to the necrotrophic fungus Botrytis cinerea is affected by plant N availability, with higher susceptibility in nitrate-limiting conditions. Global gene expression responses of tomato against B. cinerea under contrasting nitrate conditions reveals that plant primary metabolism is affected by the fungal infection regardless of N regimes. This result suggests that differential susceptibility to pathogen attack under contrasting N conditions is not only explained by a metabolic alteration. We used a systems biology approach to identify the transcriptional regulatory network implicated in plant response to the fungus infection under contrasting nitrate conditions. Interestingly, hub genes in this network are known key transcription factors involved in ethylene and jasmonic acid signaling. This result positions these hormones as key integrators of nitrate and defense against B. cinerea in tomato plants. Our results provide insights into potential crosstalk mechanisms between necrotrophic defense response and N status in plants.
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spelling pubmed-46318352015-11-18 Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum Vega, Andrea Canessa, Paulo Hoppe, Gustavo Retamal, Ignacio Moyano, Tomas C. Canales, Javier Gutiérrez, Rodrigo A. Rubilar, Joselyn Front Plant Sci Plant Science Nitrogen (N) is one of the main limiting nutrients for plant growth and crop yield. It is well documented that changes in nitrate availability, the main N source found in agricultural soils, influences a myriad of developmental programs and processes including the plant defense response. Indeed, many agronomical reports indicate that the plant N nutritional status influences their ability to respond effectively when challenged by different pathogens. However, the molecular mechanisms involved in N-modulation of plant susceptibility to pathogens are poorly characterized. In this work, we show that Solanum lycopersicum defense response to the necrotrophic fungus Botrytis cinerea is affected by plant N availability, with higher susceptibility in nitrate-limiting conditions. Global gene expression responses of tomato against B. cinerea under contrasting nitrate conditions reveals that plant primary metabolism is affected by the fungal infection regardless of N regimes. This result suggests that differential susceptibility to pathogen attack under contrasting N conditions is not only explained by a metabolic alteration. We used a systems biology approach to identify the transcriptional regulatory network implicated in plant response to the fungus infection under contrasting nitrate conditions. Interestingly, hub genes in this network are known key transcription factors involved in ethylene and jasmonic acid signaling. This result positions these hormones as key integrators of nitrate and defense against B. cinerea in tomato plants. Our results provide insights into potential crosstalk mechanisms between necrotrophic defense response and N status in plants. Frontiers Media S.A. 2015-11-04 /pmc/articles/PMC4631835/ /pubmed/26583019 http://dx.doi.org/10.3389/fpls.2015.00911 Text en Copyright © 2015 Vega, Canessa, Hoppe, Retamal, Moyano, Canales, Gutiérrez and Rubilar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Vega, Andrea
Canessa, Paulo
Hoppe, Gustavo
Retamal, Ignacio
Moyano, Tomas C.
Canales, Javier
Gutiérrez, Rodrigo A.
Rubilar, Joselyn
Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title_full Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title_fullStr Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title_full_unstemmed Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title_short Transcriptome analysis reveals regulatory networks underlying differential susceptibility to Botrytis cinerea in response to nitrogen availability in Solanum lycopersicum
title_sort transcriptome analysis reveals regulatory networks underlying differential susceptibility to botrytis cinerea in response to nitrogen availability in solanum lycopersicum
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631835/
https://www.ncbi.nlm.nih.gov/pubmed/26583019
http://dx.doi.org/10.3389/fpls.2015.00911
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