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A spatial model of the plant circadian clock reveals design principles for coordinated timing
Individual plant cells possess a genetic network, the circadian clock, that times internal processes to the day‐night cycle. Mathematical models of the clock are typically either “whole‐plant” that ignore tissue or cell type‐specific clock behavior, or “phase‐only” that do not include molecular comp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935279/ https://www.ncbi.nlm.nih.gov/pubmed/35312157 http://dx.doi.org/10.15252/msb.202010140 |
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author | Greenwood, Mark Tokuda, Isao T Locke, James C W |
author_facet | Greenwood, Mark Tokuda, Isao T Locke, James C W |
author_sort | Greenwood, Mark |
collection | PubMed |
description | Individual plant cells possess a genetic network, the circadian clock, that times internal processes to the day‐night cycle. Mathematical models of the clock are typically either “whole‐plant” that ignore tissue or cell type‐specific clock behavior, or “phase‐only” that do not include molecular components. To address the complex spatial coordination observed in experiments, here we implemented a clock network model on a template of a seedling. In our model, the sensitivity to light varies across the plant, and cells communicate their timing via local or long‐distance sharing of clock components, causing their rhythms to couple. We found that both varied light sensitivity and long‐distance coupling could generate period differences between organs, while local coupling was required to generate the spatial waves of clock gene expression observed experimentally. We then examined our model under noisy light‐dark cycles and found that local coupling minimized timing errors caused by the noise while allowing each plant region to maintain a different clock phase. Thus, local sensitivity to environmental inputs combined with local coupling enables flexible yet robust circadian timing. |
format | Online Article Text |
id | pubmed-8935279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89352792022-03-24 A spatial model of the plant circadian clock reveals design principles for coordinated timing Greenwood, Mark Tokuda, Isao T Locke, James C W Mol Syst Biol Articles Individual plant cells possess a genetic network, the circadian clock, that times internal processes to the day‐night cycle. Mathematical models of the clock are typically either “whole‐plant” that ignore tissue or cell type‐specific clock behavior, or “phase‐only” that do not include molecular components. To address the complex spatial coordination observed in experiments, here we implemented a clock network model on a template of a seedling. In our model, the sensitivity to light varies across the plant, and cells communicate their timing via local or long‐distance sharing of clock components, causing their rhythms to couple. We found that both varied light sensitivity and long‐distance coupling could generate period differences between organs, while local coupling was required to generate the spatial waves of clock gene expression observed experimentally. We then examined our model under noisy light‐dark cycles and found that local coupling minimized timing errors caused by the noise while allowing each plant region to maintain a different clock phase. Thus, local sensitivity to environmental inputs combined with local coupling enables flexible yet robust circadian timing. John Wiley and Sons Inc. 2022-03-21 /pmc/articles/PMC8935279/ /pubmed/35312157 http://dx.doi.org/10.15252/msb.202010140 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Greenwood, Mark Tokuda, Isao T Locke, James C W A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title | A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title_full | A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title_fullStr | A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title_full_unstemmed | A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title_short | A spatial model of the plant circadian clock reveals design principles for coordinated timing |
title_sort | spatial model of the plant circadian clock reveals design principles for coordinated timing |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935279/ https://www.ncbi.nlm.nih.gov/pubmed/35312157 http://dx.doi.org/10.15252/msb.202010140 |
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