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Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature

Clock-regulated pathways coordinate the response of many developmental processes to changes in photoperiod and temperature. We model two of the best-understood clock output pathways in Arabidopsis, which control key regulators of flowering and elongation growth. In flowering, the model predicted reg...

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Autores principales: Seaton, Daniel D, Smith, Robert W, Song, Young Hun, MacGregor, Dana R, Stewart, Kelly, Steel, Gavin, Foreman, Julia, Penfield, Steven, Imaizumi, Takato, Millar, Andrew J, Halliday, Karen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332151/
https://www.ncbi.nlm.nih.gov/pubmed/25600997
http://dx.doi.org/10.15252/msb.20145766
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author Seaton, Daniel D
Smith, Robert W
Song, Young Hun
MacGregor, Dana R
Stewart, Kelly
Steel, Gavin
Foreman, Julia
Penfield, Steven
Imaizumi, Takato
Millar, Andrew J
Halliday, Karen J
author_facet Seaton, Daniel D
Smith, Robert W
Song, Young Hun
MacGregor, Dana R
Stewart, Kelly
Steel, Gavin
Foreman, Julia
Penfield, Steven
Imaizumi, Takato
Millar, Andrew J
Halliday, Karen J
author_sort Seaton, Daniel D
collection PubMed
description Clock-regulated pathways coordinate the response of many developmental processes to changes in photoperiod and temperature. We model two of the best-understood clock output pathways in Arabidopsis, which control key regulators of flowering and elongation growth. In flowering, the model predicted regulatory links from the clock to CYCLING DOF FACTOR 1 (CDF1) and FLAVIN-BINDING, KELCH REPEAT, F-BOX 1 (FKF1) transcription. Physical interaction data support these links, which create threefold feed-forward motifs from two clock components to the floral regulator FT. In hypocotyl growth, the model described clock-regulated transcription of PHYTOCHROME-INTERACTING FACTOR 4 and 5 (PIF4, PIF5), interacting with post-translational regulation of PIF proteins by phytochrome B (phyB) and other light-activated pathways. The model predicted bimodal and end-of-day PIF activity profiles that are observed across hundreds of PIF-regulated target genes. In the response to temperature, warmth-enhanced PIF4 activity explained the observed hypocotyl growth dynamics but additional, temperature-dependent regulators were implicated in the flowering response. Integrating these two pathways with the clock model highlights the molecular mechanisms that coordinate plant development across changing conditions.
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spelling pubmed-43321512015-03-09 Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature Seaton, Daniel D Smith, Robert W Song, Young Hun MacGregor, Dana R Stewart, Kelly Steel, Gavin Foreman, Julia Penfield, Steven Imaizumi, Takato Millar, Andrew J Halliday, Karen J Mol Syst Biol Articles Clock-regulated pathways coordinate the response of many developmental processes to changes in photoperiod and temperature. We model two of the best-understood clock output pathways in Arabidopsis, which control key regulators of flowering and elongation growth. In flowering, the model predicted regulatory links from the clock to CYCLING DOF FACTOR 1 (CDF1) and FLAVIN-BINDING, KELCH REPEAT, F-BOX 1 (FKF1) transcription. Physical interaction data support these links, which create threefold feed-forward motifs from two clock components to the floral regulator FT. In hypocotyl growth, the model described clock-regulated transcription of PHYTOCHROME-INTERACTING FACTOR 4 and 5 (PIF4, PIF5), interacting with post-translational regulation of PIF proteins by phytochrome B (phyB) and other light-activated pathways. The model predicted bimodal and end-of-day PIF activity profiles that are observed across hundreds of PIF-regulated target genes. In the response to temperature, warmth-enhanced PIF4 activity explained the observed hypocotyl growth dynamics but additional, temperature-dependent regulators were implicated in the flowering response. Integrating these two pathways with the clock model highlights the molecular mechanisms that coordinate plant development across changing conditions. BlackWell Publishing Ltd 2015-01-19 /pmc/articles/PMC4332151/ /pubmed/25600997 http://dx.doi.org/10.15252/msb.20145766 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Seaton, Daniel D
Smith, Robert W
Song, Young Hun
MacGregor, Dana R
Stewart, Kelly
Steel, Gavin
Foreman, Julia
Penfield, Steven
Imaizumi, Takato
Millar, Andrew J
Halliday, Karen J
Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title_full Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title_fullStr Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title_full_unstemmed Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title_short Linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
title_sort linked circadian outputs control elongation growth and flowering in response to photoperiod and temperature
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332151/
https://www.ncbi.nlm.nih.gov/pubmed/25600997
http://dx.doi.org/10.15252/msb.20145766
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