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Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs
Plants resist infection and herbivory with innate immune responses that are often associated with reduced growth. Despite the importance of growth-defense tradeoffs in shaping plant productivity in natural and agricultural ecosystems, the molecular mechanisms that link growth and immunity are poorly...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155487/ https://www.ncbi.nlm.nih.gov/pubmed/27573094 http://dx.doi.org/10.1038/ncomms12570 |
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author | Campos, Marcelo L. Yoshida, Yuki Major, Ian T. de Oliveira Ferreira, Dalton Weraduwage, Sarathi M. Froehlich, John E. Johnson, Brendan F. Kramer, David M. Jander, Georg Sharkey, Thomas D. Howe, Gregg A. |
author_facet | Campos, Marcelo L. Yoshida, Yuki Major, Ian T. de Oliveira Ferreira, Dalton Weraduwage, Sarathi M. Froehlich, John E. Johnson, Brendan F. Kramer, David M. Jander, Georg Sharkey, Thomas D. Howe, Gregg A. |
author_sort | Campos, Marcelo L. |
collection | PubMed |
description | Plants resist infection and herbivory with innate immune responses that are often associated with reduced growth. Despite the importance of growth-defense tradeoffs in shaping plant productivity in natural and agricultural ecosystems, the molecular mechanisms that link growth and immunity are poorly understood. Here, we demonstrate that growth-defense tradeoffs mediated by the hormone jasmonate are uncoupled in an Arabidopsis mutant (jazQ phyB) lacking a quintet of Jasmonate ZIM-domain transcriptional repressors and the photoreceptor phyB. Analysis of epistatic interactions between jazQ and phyB reveal that growth inhibition associated with enhanced anti-insect resistance is likely not caused by diversion of photoassimilates from growth to defense but rather by a conserved transcriptional network that is hardwired to attenuate growth upon activation of jasmonate signalling. The ability to unlock growth-defense tradeoffs through relief of transcription repression provides an approach to assemble functional plant traits in new and potentially useful ways. |
format | Online Article Text |
id | pubmed-5155487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51554872016-12-21 Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs Campos, Marcelo L. Yoshida, Yuki Major, Ian T. de Oliveira Ferreira, Dalton Weraduwage, Sarathi M. Froehlich, John E. Johnson, Brendan F. Kramer, David M. Jander, Georg Sharkey, Thomas D. Howe, Gregg A. Nat Commun Article Plants resist infection and herbivory with innate immune responses that are often associated with reduced growth. Despite the importance of growth-defense tradeoffs in shaping plant productivity in natural and agricultural ecosystems, the molecular mechanisms that link growth and immunity are poorly understood. Here, we demonstrate that growth-defense tradeoffs mediated by the hormone jasmonate are uncoupled in an Arabidopsis mutant (jazQ phyB) lacking a quintet of Jasmonate ZIM-domain transcriptional repressors and the photoreceptor phyB. Analysis of epistatic interactions between jazQ and phyB reveal that growth inhibition associated with enhanced anti-insect resistance is likely not caused by diversion of photoassimilates from growth to defense but rather by a conserved transcriptional network that is hardwired to attenuate growth upon activation of jasmonate signalling. The ability to unlock growth-defense tradeoffs through relief of transcription repression provides an approach to assemble functional plant traits in new and potentially useful ways. Nature Publishing Group 2016-08-30 /pmc/articles/PMC5155487/ /pubmed/27573094 http://dx.doi.org/10.1038/ncomms12570 Text en Copyright © 2016, 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 Campos, Marcelo L. Yoshida, Yuki Major, Ian T. de Oliveira Ferreira, Dalton Weraduwage, Sarathi M. Froehlich, John E. Johnson, Brendan F. Kramer, David M. Jander, Georg Sharkey, Thomas D. Howe, Gregg A. Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title | Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title_full | Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title_fullStr | Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title_full_unstemmed | Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title_short | Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs |
title_sort | rewiring of jasmonate and phytochrome b signalling uncouples plant growth-defense tradeoffs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155487/ https://www.ncbi.nlm.nih.gov/pubmed/27573094 http://dx.doi.org/10.1038/ncomms12570 |
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