Cargando…

PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation

Dormancy cycling controls the seasonal conditions under which seeds germinate, and these conditions strongly influence growth and survival of plants. Several endogenous and environmental signals affect the dormancy status of seeds. Factors such as time, light, and temperature influence the balance b...

Descripción completa

Detalles Bibliográficos
Autores principales: Martel, Catherine, Blair, Logan K, Donohue, Kathleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972622/
https://www.ncbi.nlm.nih.gov/pubmed/29648603
http://dx.doi.org/10.1093/jxb/ery140
_version_ 1783326459390066688
author Martel, Catherine
Blair, Logan K
Donohue, Kathleen
author_facet Martel, Catherine
Blair, Logan K
Donohue, Kathleen
author_sort Martel, Catherine
collection PubMed
description Dormancy cycling controls the seasonal conditions under which seeds germinate, and these conditions strongly influence growth and survival of plants. Several endogenous and environmental signals affect the dormancy status of seeds. Factors such as time, light, and temperature influence the balance between abscisic acid (ABA) and gibberellic acid (GA), two phytohormones that play a key role in seed dormancy and germination. High temperatures have been shown to increase ABA level and prevent seed germination, a process known as thermoinhibition. High temperature can also cause the acquisition of secondary dormancy, preventing germination of seeds upon their return to favorable germination conditions. The mechanisms and conditions linking thermoinhibition and secondary dormancy remain unclear. Phytochromes are photoreceptors known to promote seed germination of many plant species including Arabidopsis thaliana. Here, we demonstrate a role for PHYD in modulating secondary dormancy acquisition in seeds exposed to high temperature. We found that a functional PHYD gene is required for the germination of seeds that experienced high temperature, and that ABA- and GA-related gene expression during and after pre-incubation at high temperatures was altered in a phyD mutant. We further show that the level of PHYD mRNA increased in seeds pre-incubated at high temperature and that this increase correlates with efficient removal of the germination repressor PIL5.
format Online
Article
Text
id pubmed-5972622
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-59726222018-06-04 PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation Martel, Catherine Blair, Logan K Donohue, Kathleen J Exp Bot Research Papers Dormancy cycling controls the seasonal conditions under which seeds germinate, and these conditions strongly influence growth and survival of plants. Several endogenous and environmental signals affect the dormancy status of seeds. Factors such as time, light, and temperature influence the balance between abscisic acid (ABA) and gibberellic acid (GA), two phytohormones that play a key role in seed dormancy and germination. High temperatures have been shown to increase ABA level and prevent seed germination, a process known as thermoinhibition. High temperature can also cause the acquisition of secondary dormancy, preventing germination of seeds upon their return to favorable germination conditions. The mechanisms and conditions linking thermoinhibition and secondary dormancy remain unclear. Phytochromes are photoreceptors known to promote seed germination of many plant species including Arabidopsis thaliana. Here, we demonstrate a role for PHYD in modulating secondary dormancy acquisition in seeds exposed to high temperature. We found that a functional PHYD gene is required for the germination of seeds that experienced high temperature, and that ABA- and GA-related gene expression during and after pre-incubation at high temperatures was altered in a phyD mutant. We further show that the level of PHYD mRNA increased in seeds pre-incubated at high temperature and that this increase correlates with efficient removal of the germination repressor PIL5. Oxford University Press 2018-05-25 2018-04-10 /pmc/articles/PMC5972622/ /pubmed/29648603 http://dx.doi.org/10.1093/jxb/ery140 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Martel, Catherine
Blair, Logan K
Donohue, Kathleen
PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title_full PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title_fullStr PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title_full_unstemmed PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title_short PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
title_sort phyd prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower pil5 accumulation
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972622/
https://www.ncbi.nlm.nih.gov/pubmed/29648603
http://dx.doi.org/10.1093/jxb/ery140
work_keys_str_mv AT martelcatherine phydpreventssecondarydormancyestablishmentofseedsexposedtohightemperatureandisassociatedwithlowerpil5accumulation
AT blairlogank phydpreventssecondarydormancyestablishmentofseedsexposedtohightemperatureandisassociatedwithlowerpil5accumulation
AT donohuekathleen phydpreventssecondarydormancyestablishmentofseedsexposedtohightemperatureandisassociatedwithlowerpil5accumulation