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A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
Environmental signals drive seed dormancy cycling in the soil to synchronize germination with the optimal time of year, a process essential for species' fitness and survival. Previous correlation of transcription profiles in exhumed seeds with annual environmental signals revealed the coordinat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518234/ https://www.ncbi.nlm.nih.gov/pubmed/28240777 http://dx.doi.org/10.1111/pce.12940 |
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author | Footitt, Steven Ölçer‐Footitt, Hülya Hambidge, Angela J. Finch‐Savage, William E. |
author_facet | Footitt, Steven Ölçer‐Footitt, Hülya Hambidge, Angela J. Finch‐Savage, William E. |
author_sort | Footitt, Steven |
collection | PubMed |
description | Environmental signals drive seed dormancy cycling in the soil to synchronize germination with the optimal time of year, a process essential for species' fitness and survival. Previous correlation of transcription profiles in exhumed seeds with annual environmental signals revealed the coordination of dormancy‐regulating mechanisms with the soil environment. Here, we developed a rapid and robust laboratory dormancy cycling simulation. The utility of this simulation was tested in two ways: firstly, using mutants in known dormancy‐related genes [DELAY OF GERMINATION 1 (DOG1), MOTHER OF FLOWERING TIME (MFT), CBL‐INTERACTING PROTEIN KINASE 23 (CIPK23) and PHYTOCHROME A (PHYA)] and secondly, using further mutants, we test the hypothesis that components of the circadian clock are involved in coordination of the annual seed dormancy cycle. The rate of dormancy induction and relief differed in all lines tested. In the mutants, dog1‐2 and mft2, dormancy induction was reduced but not absent. DOG1 is not absolutely required for dormancy. In cipk23 and phyA dormancy, induction was accelerated. Involvement of the clock in dormancy cycling was clear when mutants in the morning and evening loops of the clock were compared. Dormancy induction was faster when the morning loop was compromised and delayed when the evening loop was compromised. |
format | Online Article Text |
id | pubmed-5518234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55182342017-08-03 A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA Footitt, Steven Ölçer‐Footitt, Hülya Hambidge, Angela J. Finch‐Savage, William E. Plant Cell Environ Original Articles Environmental signals drive seed dormancy cycling in the soil to synchronize germination with the optimal time of year, a process essential for species' fitness and survival. Previous correlation of transcription profiles in exhumed seeds with annual environmental signals revealed the coordination of dormancy‐regulating mechanisms with the soil environment. Here, we developed a rapid and robust laboratory dormancy cycling simulation. The utility of this simulation was tested in two ways: firstly, using mutants in known dormancy‐related genes [DELAY OF GERMINATION 1 (DOG1), MOTHER OF FLOWERING TIME (MFT), CBL‐INTERACTING PROTEIN KINASE 23 (CIPK23) and PHYTOCHROME A (PHYA)] and secondly, using further mutants, we test the hypothesis that components of the circadian clock are involved in coordination of the annual seed dormancy cycle. The rate of dormancy induction and relief differed in all lines tested. In the mutants, dog1‐2 and mft2, dormancy induction was reduced but not absent. DOG1 is not absolutely required for dormancy. In cipk23 and phyA dormancy, induction was accelerated. Involvement of the clock in dormancy cycling was clear when mutants in the morning and evening loops of the clock were compared. Dormancy induction was faster when the morning loop was compromised and delayed when the evening loop was compromised. John Wiley and Sons Inc. 2017-05-16 2017-08 /pmc/articles/PMC5518234/ /pubmed/28240777 http://dx.doi.org/10.1111/pce.12940 Text en © 2017 The Authors Plant, Cell & Environment Published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Footitt, Steven Ölçer‐Footitt, Hülya Hambidge, Angela J. Finch‐Savage, William E. A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA |
title | A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
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title_full | A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
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title_fullStr | A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
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title_full_unstemmed | A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
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title_short | A laboratory simulation of Arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes DOG1, MFT, CIPK23 and PHYA
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title_sort | laboratory simulation of arabidopsis seed dormancy cycling provides new insight into its regulation by clock genes and the dormancy‐related genes dog1, mft, cipk23 and phya |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518234/ https://www.ncbi.nlm.nih.gov/pubmed/28240777 http://dx.doi.org/10.1111/pce.12940 |
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