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The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB
Seed thermoinhibition, the repression of germination under high temperatures, prevents seedling establishment under potentially fatal conditions. Thermoinhibition is relevant for phenology and agriculture, particularly in a warming globe. The temperature sensing mechanisms and signaling pathways sus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992654/ https://www.ncbi.nlm.nih.gov/pubmed/36882415 http://dx.doi.org/10.1038/s41467-023-36903-4 |
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author | Piskurewicz, Urszula Sentandreu, Maria Iwasaki, Mayumi Glauser, Gaëtan Lopez-Molina, Luis |
author_facet | Piskurewicz, Urszula Sentandreu, Maria Iwasaki, Mayumi Glauser, Gaëtan Lopez-Molina, Luis |
author_sort | Piskurewicz, Urszula |
collection | PubMed |
description | Seed thermoinhibition, the repression of germination under high temperatures, prevents seedling establishment under potentially fatal conditions. Thermoinhibition is relevant for phenology and agriculture, particularly in a warming globe. The temperature sensing mechanisms and signaling pathways sustaining thermoinhibition are unknown. Here we show that thermoinhibition in Arabidopsis thaliana is not autonomously controlled by the embryo but is rather implemented by the endosperm. High temperature is sensed through endospermic phyB by accelerating its reversion from the active signaling Pfr form into the inactive Pr form, as previously described in seedlings. This leads to thermoinhibition mediated by PIFs, mainly PIF1, PIF3 and PIF5. Endospermic PIF3 represses the expression of the endospermic ABA catabolic gene CYP707A1 and promotes endospermic ABA accumulation and release towards the embryo to block its growth. Furthermore, endospermic ABA represses embryonic PIF3 accumulation that would otherwise promote embryonic growth. Hence, under high temperatures PIF3 exerts opposite growth responses in the endosperm and embryo. |
format | Online Article Text |
id | pubmed-9992654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99926542023-03-09 The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB Piskurewicz, Urszula Sentandreu, Maria Iwasaki, Mayumi Glauser, Gaëtan Lopez-Molina, Luis Nat Commun Article Seed thermoinhibition, the repression of germination under high temperatures, prevents seedling establishment under potentially fatal conditions. Thermoinhibition is relevant for phenology and agriculture, particularly in a warming globe. The temperature sensing mechanisms and signaling pathways sustaining thermoinhibition are unknown. Here we show that thermoinhibition in Arabidopsis thaliana is not autonomously controlled by the embryo but is rather implemented by the endosperm. High temperature is sensed through endospermic phyB by accelerating its reversion from the active signaling Pfr form into the inactive Pr form, as previously described in seedlings. This leads to thermoinhibition mediated by PIFs, mainly PIF1, PIF3 and PIF5. Endospermic PIF3 represses the expression of the endospermic ABA catabolic gene CYP707A1 and promotes endospermic ABA accumulation and release towards the embryo to block its growth. Furthermore, endospermic ABA represses embryonic PIF3 accumulation that would otherwise promote embryonic growth. Hence, under high temperatures PIF3 exerts opposite growth responses in the endosperm and embryo. Nature Publishing Group UK 2023-03-07 /pmc/articles/PMC9992654/ /pubmed/36882415 http://dx.doi.org/10.1038/s41467-023-36903-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Piskurewicz, Urszula Sentandreu, Maria Iwasaki, Mayumi Glauser, Gaëtan Lopez-Molina, Luis The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title | The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title_full | The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title_fullStr | The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title_full_unstemmed | The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title_short | The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB |
title_sort | arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyb |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992654/ https://www.ncbi.nlm.nih.gov/pubmed/36882415 http://dx.doi.org/10.1038/s41467-023-36903-4 |
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