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The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth
Adjustment to energy starvation is crucial to ensure growth and survival. In Arabidopsis thaliana (Arabidopsis), this process relies in part on the phosphorylation of the circadian clock regulator bZIP63 by SUCROSE non‐fermenting RELATED KINASE1 (SnRK1), a key mediator of responses to low energy. We...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292441/ https://www.ncbi.nlm.nih.gov/pubmed/34053087 http://dx.doi.org/10.1111/nph.17518 |
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author | Viana, Américo J. C. Matiolli, Cleverson C. Newman, David W. Vieira, João G. P. Duarte, Gustavo T. Martins, Marina C. M. Gilbault, Elodie Hotta, Carlos T. Caldana, Camila Vincentz, Michel |
author_facet | Viana, Américo J. C. Matiolli, Cleverson C. Newman, David W. Vieira, João G. P. Duarte, Gustavo T. Martins, Marina C. M. Gilbault, Elodie Hotta, Carlos T. Caldana, Camila Vincentz, Michel |
author_sort | Viana, Américo J. C. |
collection | PubMed |
description | Adjustment to energy starvation is crucial to ensure growth and survival. In Arabidopsis thaliana (Arabidopsis), this process relies in part on the phosphorylation of the circadian clock regulator bZIP63 by SUCROSE non‐fermenting RELATED KINASE1 (SnRK1), a key mediator of responses to low energy. We investigated the effects of mutations in bZIP63 on plant carbon (C) metabolism and growth. Results from phenotypic, transcriptomic and metabolomic analysis of bZIP63 mutants prompted us to investigate the starch accumulation pattern and the expression of genes involved in starch degradation and in the circadian oscillator. bZIP63 mutation impairs growth under light‐dark cycles, but not under constant light. The reduced growth likely results from the accentuated C depletion towards the end of the night, which is caused by the accelerated starch degradation of bZIP63 mutants. The diel expression pattern of bZIP63 is dictated by both the circadian clock and energy levels, which could determine the changes in the circadian expression of clock and starch metabolic genes observed in bZIP63 mutants. We conclude that bZIP63 composes a regulatory interface between the metabolic and circadian control of starch breakdown to optimize C usage and plant growth. |
format | Online Article Text |
id | pubmed-9292441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92924412022-07-20 The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth Viana, Américo J. C. Matiolli, Cleverson C. Newman, David W. Vieira, João G. P. Duarte, Gustavo T. Martins, Marina C. M. Gilbault, Elodie Hotta, Carlos T. Caldana, Camila Vincentz, Michel New Phytol Research Adjustment to energy starvation is crucial to ensure growth and survival. In Arabidopsis thaliana (Arabidopsis), this process relies in part on the phosphorylation of the circadian clock regulator bZIP63 by SUCROSE non‐fermenting RELATED KINASE1 (SnRK1), a key mediator of responses to low energy. We investigated the effects of mutations in bZIP63 on plant carbon (C) metabolism and growth. Results from phenotypic, transcriptomic and metabolomic analysis of bZIP63 mutants prompted us to investigate the starch accumulation pattern and the expression of genes involved in starch degradation and in the circadian oscillator. bZIP63 mutation impairs growth under light‐dark cycles, but not under constant light. The reduced growth likely results from the accentuated C depletion towards the end of the night, which is caused by the accelerated starch degradation of bZIP63 mutants. The diel expression pattern of bZIP63 is dictated by both the circadian clock and energy levels, which could determine the changes in the circadian expression of clock and starch metabolic genes observed in bZIP63 mutants. We conclude that bZIP63 composes a regulatory interface between the metabolic and circadian control of starch breakdown to optimize C usage and plant growth. John Wiley and Sons Inc. 2021-06-30 2021-09 /pmc/articles/PMC9292441/ /pubmed/34053087 http://dx.doi.org/10.1111/nph.17518 Text en © 2021 The Authors New Phytologist © 2021 New Phytologist Foundation 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 | Research Viana, Américo J. C. Matiolli, Cleverson C. Newman, David W. Vieira, João G. P. Duarte, Gustavo T. Martins, Marina C. M. Gilbault, Elodie Hotta, Carlos T. Caldana, Camila Vincentz, Michel The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title | The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title_full | The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title_fullStr | The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title_full_unstemmed | The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title_short | The sugar‐responsive circadian clock regulator bZIP63 modulates plant growth |
title_sort | sugar‐responsive circadian clock regulator bzip63 modulates plant growth |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292441/ https://www.ncbi.nlm.nih.gov/pubmed/34053087 http://dx.doi.org/10.1111/nph.17518 |
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