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PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis
Plants react to seasonal change in day length through altering physiology and development. Factors that function to harmonize growth with photoperiod are poorly understood. Here we characterize a new protein that associates with both circadian clock and photoreceptor components, named PHOTOPERIODIC...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755757/ https://www.ncbi.nlm.nih.gov/pubmed/26839287 http://dx.doi.org/10.7554/eLife.13292 |
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author | Huang, He Yoo, Chan Yul Bindbeutel, Rebecca Goldsworthy, Jessica Tielking, Allison Alvarez, Sophie Naldrett, Michael J Evans, Bradley S Chen, Meng Nusinow, Dmitri A |
author_facet | Huang, He Yoo, Chan Yul Bindbeutel, Rebecca Goldsworthy, Jessica Tielking, Allison Alvarez, Sophie Naldrett, Michael J Evans, Bradley S Chen, Meng Nusinow, Dmitri A |
author_sort | Huang, He |
collection | PubMed |
description | Plants react to seasonal change in day length through altering physiology and development. Factors that function to harmonize growth with photoperiod are poorly understood. Here we characterize a new protein that associates with both circadian clock and photoreceptor components, named PHOTOPERIODIC CONTROL OF HYPOCOTYL1 (PCH1). pch1 seedlings have overly elongated hypocotyls specifically under short days while constitutive expression of PCH1 shortens hypocotyls independent of day length. PCH1 peaks at dusk, binds phytochrome B (phyB) in a red light-dependent manner, and co-localizes with phyB into photobodies. PCH1 is necessary and sufficient to promote the biogenesis of large photobodies to maintain an active phyB pool after light exposure, potentiating red-light signaling and prolonging memory of prior illumination. Manipulating PCH1 alters PHYTOCHROME INTERACTING FACTOR 4 levels and regulates light-responsive gene expression. Thus, PCH1 is a new factor that regulates photoperiod-responsive growth by integrating the clock with light perception pathways through modulating daily phyB-signaling. DOI: http://dx.doi.org/10.7554/eLife.13292.001 |
format | Online Article Text |
id | pubmed-4755757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47557572016-02-18 PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis Huang, He Yoo, Chan Yul Bindbeutel, Rebecca Goldsworthy, Jessica Tielking, Allison Alvarez, Sophie Naldrett, Michael J Evans, Bradley S Chen, Meng Nusinow, Dmitri A eLife Plant Biology Plants react to seasonal change in day length through altering physiology and development. Factors that function to harmonize growth with photoperiod are poorly understood. Here we characterize a new protein that associates with both circadian clock and photoreceptor components, named PHOTOPERIODIC CONTROL OF HYPOCOTYL1 (PCH1). pch1 seedlings have overly elongated hypocotyls specifically under short days while constitutive expression of PCH1 shortens hypocotyls independent of day length. PCH1 peaks at dusk, binds phytochrome B (phyB) in a red light-dependent manner, and co-localizes with phyB into photobodies. PCH1 is necessary and sufficient to promote the biogenesis of large photobodies to maintain an active phyB pool after light exposure, potentiating red-light signaling and prolonging memory of prior illumination. Manipulating PCH1 alters PHYTOCHROME INTERACTING FACTOR 4 levels and regulates light-responsive gene expression. Thus, PCH1 is a new factor that regulates photoperiod-responsive growth by integrating the clock with light perception pathways through modulating daily phyB-signaling. DOI: http://dx.doi.org/10.7554/eLife.13292.001 eLife Sciences Publications, Ltd 2016-02-03 /pmc/articles/PMC4755757/ /pubmed/26839287 http://dx.doi.org/10.7554/eLife.13292 Text en © 2016, Huang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Plant Biology Huang, He Yoo, Chan Yul Bindbeutel, Rebecca Goldsworthy, Jessica Tielking, Allison Alvarez, Sophie Naldrett, Michael J Evans, Bradley S Chen, Meng Nusinow, Dmitri A PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title | PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title_full | PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title_fullStr | PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title_full_unstemmed | PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title_short | PCH1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in Arabidopsis |
title_sort | pch1 integrates circadian and light-signaling pathways to control photoperiod-responsive growth in arabidopsis |
topic | Plant Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755757/ https://www.ncbi.nlm.nih.gov/pubmed/26839287 http://dx.doi.org/10.7554/eLife.13292 |
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