Cargando…
The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels
BACKGROUND: In seeds, the transition from dormancy to germination is regulated by abscisic acid (ABA) and gibberellins (GAs), and involves chromatin remodelling. Particularly, the repressive mark H3K27 trimethylation (H3K27me3) has been shown to target many master regulators of this transition. DAG1...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016951/ https://www.ncbi.nlm.nih.gov/pubmed/27613195 http://dx.doi.org/10.1186/s12870-016-0890-5 |
_version_ | 1782452654276870144 |
---|---|
author | Boccaccini, Alessandra Lorrai, Riccardo Ruta, Veronica Frey, Anne Mercey-Boutet, Stephanie Marion-Poll, Annie Tarkowská, Danuše Strnad, Miroslav Costantino, Paolo Vittorioso, Paola |
author_facet | Boccaccini, Alessandra Lorrai, Riccardo Ruta, Veronica Frey, Anne Mercey-Boutet, Stephanie Marion-Poll, Annie Tarkowská, Danuše Strnad, Miroslav Costantino, Paolo Vittorioso, Paola |
author_sort | Boccaccini, Alessandra |
collection | PubMed |
description | BACKGROUND: In seeds, the transition from dormancy to germination is regulated by abscisic acid (ABA) and gibberellins (GAs), and involves chromatin remodelling. Particularly, the repressive mark H3K27 trimethylation (H3K27me3) has been shown to target many master regulators of this transition. DAG1 (DOF AFFECTING GERMINATION1), is a negative regulator of seed germination in Arabidopsis, and directly represses the GA biosynthetic gene GA3ox1 (gibberellin 3-β-dioxygenase 1). We set to investigate the role of DAG1 in seed dormancy and maturation with respect to epigenetic and hormonal control. RESULTS: We show that DAG1 expression is controlled at the epigenetic level through the H3K27me3 mark during the seed-to-seedling transition, and that DAG1 directly represses also the ABA catabolic gene CYP707A2; consistently, the ABA level is lower while the GA level is higher in dag1 mutant seeds. Furthermore, both DAG1 expression and protein stability are controlled by GAs. CONCLUSIONS: Our results point to DAG1 as a key player in the control of the developmental switch between seed dormancy and germination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0890-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5016951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50169512016-09-10 The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels Boccaccini, Alessandra Lorrai, Riccardo Ruta, Veronica Frey, Anne Mercey-Boutet, Stephanie Marion-Poll, Annie Tarkowská, Danuše Strnad, Miroslav Costantino, Paolo Vittorioso, Paola BMC Plant Biol Research Article BACKGROUND: In seeds, the transition from dormancy to germination is regulated by abscisic acid (ABA) and gibberellins (GAs), and involves chromatin remodelling. Particularly, the repressive mark H3K27 trimethylation (H3K27me3) has been shown to target many master regulators of this transition. DAG1 (DOF AFFECTING GERMINATION1), is a negative regulator of seed germination in Arabidopsis, and directly represses the GA biosynthetic gene GA3ox1 (gibberellin 3-β-dioxygenase 1). We set to investigate the role of DAG1 in seed dormancy and maturation with respect to epigenetic and hormonal control. RESULTS: We show that DAG1 expression is controlled at the epigenetic level through the H3K27me3 mark during the seed-to-seedling transition, and that DAG1 directly represses also the ABA catabolic gene CYP707A2; consistently, the ABA level is lower while the GA level is higher in dag1 mutant seeds. Furthermore, both DAG1 expression and protein stability are controlled by GAs. CONCLUSIONS: Our results point to DAG1 as a key player in the control of the developmental switch between seed dormancy and germination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-016-0890-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-09 /pmc/articles/PMC5016951/ /pubmed/27613195 http://dx.doi.org/10.1186/s12870-016-0890-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Boccaccini, Alessandra Lorrai, Riccardo Ruta, Veronica Frey, Anne Mercey-Boutet, Stephanie Marion-Poll, Annie Tarkowská, Danuše Strnad, Miroslav Costantino, Paolo Vittorioso, Paola The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title | The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title_full | The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title_fullStr | The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title_full_unstemmed | The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title_short | The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels |
title_sort | dag1 transcription factor negatively regulates the seed-to-seedling transition in arabidopsis acting on aba and ga levels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016951/ https://www.ncbi.nlm.nih.gov/pubmed/27613195 http://dx.doi.org/10.1186/s12870-016-0890-5 |
work_keys_str_mv | AT boccaccinialessandra thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT lorrairiccardo thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT rutaveronica thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT freyanne thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT merceyboutetstephanie thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT marionpollannie thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT tarkowskadanuse thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT strnadmiroslav thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT costantinopaolo thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT vittoriosopaola thedag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT boccaccinialessandra dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT lorrairiccardo dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT rutaveronica dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT freyanne dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT merceyboutetstephanie dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT marionpollannie dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT tarkowskadanuse dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT strnadmiroslav dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT costantinopaolo dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels AT vittoriosopaola dag1transcriptionfactornegativelyregulatestheseedtoseedlingtransitioninarabidopsisactingonabaandgalevels |