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Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network

Plastid-to-nucleus retrograde signals emitted by dysfunctional chloroplasts impact photomorphogenic development, but the molecular link between retrograde- and photosensory-receptor signalling has remained unclear. Here, we show that the phytochrome and retrograde signalling (RS) pathways converge a...

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Autores principales: Martín, Guiomar, Leivar, Pablo, Ludevid, Dolores, Tepperman, James M., Quail, Peter H., Monte, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859062/
https://www.ncbi.nlm.nih.gov/pubmed/27150909
http://dx.doi.org/10.1038/ncomms11431
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author Martín, Guiomar
Leivar, Pablo
Ludevid, Dolores
Tepperman, James M.
Quail, Peter H.
Monte, Elena
author_facet Martín, Guiomar
Leivar, Pablo
Ludevid, Dolores
Tepperman, James M.
Quail, Peter H.
Monte, Elena
author_sort Martín, Guiomar
collection PubMed
description Plastid-to-nucleus retrograde signals emitted by dysfunctional chloroplasts impact photomorphogenic development, but the molecular link between retrograde- and photosensory-receptor signalling has remained unclear. Here, we show that the phytochrome and retrograde signalling (RS) pathways converge antagonistically to regulate the expression of the nuclear-encoded transcription factor GLK1, a key regulator of a light-induced transcriptional network central to photomorphogenesis. GLK1 gene transcription is directly repressed by PHYTOCHROME-INTERACTING FACTOR (PIF)-class bHLH transcription factors in darkness, but light-activated phytochrome reverses this activity, thereby inducing expression. Conversely, we show that retrograde signals repress this induction by a mechanism independent of PIF mediation. Collectively, our data indicate that light at moderate levels acts through the plant's nuclear-localized sensory-photoreceptor system to induce appropriate photomorphogenic development, but at excessive levels, sensed through the separate plastid-localized RS system, acts to suppress such development, thus providing a mechanism for protection against photo-oxidative damage by minimizing the tissue exposure to deleterious radiation.
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spelling pubmed-48590622016-05-23 Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network Martín, Guiomar Leivar, Pablo Ludevid, Dolores Tepperman, James M. Quail, Peter H. Monte, Elena Nat Commun Article Plastid-to-nucleus retrograde signals emitted by dysfunctional chloroplasts impact photomorphogenic development, but the molecular link between retrograde- and photosensory-receptor signalling has remained unclear. Here, we show that the phytochrome and retrograde signalling (RS) pathways converge antagonistically to regulate the expression of the nuclear-encoded transcription factor GLK1, a key regulator of a light-induced transcriptional network central to photomorphogenesis. GLK1 gene transcription is directly repressed by PHYTOCHROME-INTERACTING FACTOR (PIF)-class bHLH transcription factors in darkness, but light-activated phytochrome reverses this activity, thereby inducing expression. Conversely, we show that retrograde signals repress this induction by a mechanism independent of PIF mediation. Collectively, our data indicate that light at moderate levels acts through the plant's nuclear-localized sensory-photoreceptor system to induce appropriate photomorphogenic development, but at excessive levels, sensed through the separate plastid-localized RS system, acts to suppress such development, thus providing a mechanism for protection against photo-oxidative damage by minimizing the tissue exposure to deleterious radiation. Nature Publishing Group 2016-05-06 /pmc/articles/PMC4859062/ /pubmed/27150909 http://dx.doi.org/10.1038/ncomms11431 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Martín, Guiomar
Leivar, Pablo
Ludevid, Dolores
Tepperman, James M.
Quail, Peter H.
Monte, Elena
Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title_full Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title_fullStr Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title_full_unstemmed Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title_short Phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
title_sort phytochrome and retrograde signalling pathways converge to antagonistically regulate a light-induced transcriptional network
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859062/
https://www.ncbi.nlm.nih.gov/pubmed/27150909
http://dx.doi.org/10.1038/ncomms11431
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