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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...
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/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. |
format | Online Article Text |
id | pubmed-4859062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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