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AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis
Flowering is a dynamic and synchronized process, the timing of which is finely tuned by various environmental signals. A T-DNA insertion mutant in Arabidopsis HEAT SHOCK PROTEIN-RELATED (AtHSPR) exhibited late-flowering phenotypes under both long-day (LD) and short-day (SD) conditions compared to th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475253/ https://www.ncbi.nlm.nih.gov/pubmed/32157303 http://dx.doi.org/10.1093/jxb/eraa128 |
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author | Yang, Tao Sun, Yan Wang, Yongli Zhou, Lina Chen, Mengya Bian, Zhiyuan Lian, Yuke Xuan, Lijuan Yuan, Guoqiang Wang, Xinyu Wang, Chongying |
author_facet | Yang, Tao Sun, Yan Wang, Yongli Zhou, Lina Chen, Mengya Bian, Zhiyuan Lian, Yuke Xuan, Lijuan Yuan, Guoqiang Wang, Xinyu Wang, Chongying |
author_sort | Yang, Tao |
collection | PubMed |
description | Flowering is a dynamic and synchronized process, the timing of which is finely tuned by various environmental signals. A T-DNA insertion mutant in Arabidopsis HEAT SHOCK PROTEIN-RELATED (AtHSPR) exhibited late-flowering phenotypes under both long-day (LD) and short-day (SD) conditions compared to the wild-type, while over-expression of AtHSPR promoted flowering. Exogenous application of gibberellin (GA) partially rescued the late-flowering mutant phenotype under both LD and SD conditions, suggesting that AtHSPR is involved in GA biosynthesis and/or the GA signaling that promotes flowering. Under SD or low-light conditions, the Athspr mutant exhibited late flowering together with reduced pollen viability and seed set, defective phenotypes that were partially rescued by GA treatment. qRT-PCR assays confirmed that GA biosynthetic genes were down-regulated, that GA catabolic genes were up-regulated, and that the levels of bioactive GA and its intermediates were decreased in Athspr under both SD and low-light/LD, further suggesting that AtHSPR could be involved in the GA pathway under SD and low-light conditions. Furthermore, AtHSPR interacted in vitro with OFP1 and KNAT5, which are transcriptional repressors of GA20ox1 in GA biosynthesis. Taken together, our findings demonstrate that AtHSPR plays a positive role in GA- and light intensity-mediated regulation of flowering and seed set. |
format | Online Article Text |
id | pubmed-7475253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74752532020-09-10 AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis Yang, Tao Sun, Yan Wang, Yongli Zhou, Lina Chen, Mengya Bian, Zhiyuan Lian, Yuke Xuan, Lijuan Yuan, Guoqiang Wang, Xinyu Wang, Chongying J Exp Bot Research Papers Flowering is a dynamic and synchronized process, the timing of which is finely tuned by various environmental signals. A T-DNA insertion mutant in Arabidopsis HEAT SHOCK PROTEIN-RELATED (AtHSPR) exhibited late-flowering phenotypes under both long-day (LD) and short-day (SD) conditions compared to the wild-type, while over-expression of AtHSPR promoted flowering. Exogenous application of gibberellin (GA) partially rescued the late-flowering mutant phenotype under both LD and SD conditions, suggesting that AtHSPR is involved in GA biosynthesis and/or the GA signaling that promotes flowering. Under SD or low-light conditions, the Athspr mutant exhibited late flowering together with reduced pollen viability and seed set, defective phenotypes that were partially rescued by GA treatment. qRT-PCR assays confirmed that GA biosynthetic genes were down-regulated, that GA catabolic genes were up-regulated, and that the levels of bioactive GA and its intermediates were decreased in Athspr under both SD and low-light/LD, further suggesting that AtHSPR could be involved in the GA pathway under SD and low-light conditions. Furthermore, AtHSPR interacted in vitro with OFP1 and KNAT5, which are transcriptional repressors of GA20ox1 in GA biosynthesis. Taken together, our findings demonstrate that AtHSPR plays a positive role in GA- and light intensity-mediated regulation of flowering and seed set. Oxford University Press 2020-06-22 2020-03-10 /pmc/articles/PMC7475253/ /pubmed/32157303 http://dx.doi.org/10.1093/jxb/eraa128 Text en © The Author(s) 2020. 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 Yang, Tao Sun, Yan Wang, Yongli Zhou, Lina Chen, Mengya Bian, Zhiyuan Lian, Yuke Xuan, Lijuan Yuan, Guoqiang Wang, Xinyu Wang, Chongying AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title |
AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title_full |
AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title_fullStr |
AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title_full_unstemmed |
AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title_short |
AtHSPR is involved in GA- and light intensity-mediated control of flowering time and seed set in Arabidopsis |
title_sort | athspr is involved in ga- and light intensity-mediated control of flowering time and seed set in arabidopsis |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475253/ https://www.ncbi.nlm.nih.gov/pubmed/32157303 http://dx.doi.org/10.1093/jxb/eraa128 |
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