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The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels
A. Boccaccini, R. Lorrai, V. Ruta, A. Frey, S. Mercey-Boutet, A. Marion-Poll, D. Tarkowská, M. Strnad, P. Costantino, P. Vittorioso,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
NLK
BioMedCentral
od 2001-12-01
BioMedCentral Open Access
od 2001
Directory of Open Access Journals
od 2001
Free Medical Journals
od 2001
PubMed Central
od 2001
Europe PubMed Central
od 2001
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2001-09-01
Medline Complete (EBSCOhost)
od 2001-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
Springer Nature OA/Free Journals
od 2001-12-01
- MeSH
- Arabidopsis růst a vývoj metabolismus MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- gibereliny metabolismus MeSH
- kyselina abscisová metabolismus MeSH
- proteiny huseníčku genetika metabolismus MeSH
- semena rostlinná genetika růst a vývoj metabolismus MeSH
- semenáček genetika růst a vývoj metabolismus MeSH
- transkripční faktory genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
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.
Citace poskytuje Crossref.org
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- $a Boccaccini, Alessandra $u Istituto Pasteur Italia - Fondazione Cenci Bolognetti, Rome, Italy. Dipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185, Rome, Italy.
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- $a The DAG1 transcription factor negatively regulates the seed-to-seedling transition in Arabidopsis acting on ABA and GA levels / $c A. Boccaccini, R. Lorrai, V. Ruta, A. Frey, S. Mercey-Boutet, A. Marion-Poll, D. Tarkowská, M. Strnad, P. Costantino, P. Vittorioso,
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- $a 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.
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- $a Lorrai, Riccardo $u Istituto Pasteur Italia - Fondazione Cenci Bolognetti, Rome, Italy. Dipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185, Rome, Italy.
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- $a Frey, Anne $u Institut Jean-Pierre Bourgin, UMR1318, INRA, AgroParisTech, Université Paris-Saclay, RD10, 78026, Versailles, Cedex, France.
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- $a Mercey-Boutet, Stephanie $u Institut Jean-Pierre Bourgin, UMR1318, INRA, AgroParisTech, Université Paris-Saclay, RD10, 78026, Versailles, Cedex, France.
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- $a Marion-Poll, Annie $u Institut Jean-Pierre Bourgin, UMR1318, INRA, AgroParisTech, Université Paris-Saclay, RD10, 78026, Versailles, Cedex, France.
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- $a Tarkowská, Danuše $u Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany ASCR & Palacký University, Šlechtitelů 11, CZ-783 71, Olomouc, Czech Republic.
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- $a Costantino, Paolo $u Dipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185, Rome, Italy.
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- $a Vittorioso, Paola $u Istituto Pasteur Italia - Fondazione Cenci Bolognetti, Rome, Italy. paola.vittorioso@uniroma1.it. Dipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185, Rome, Italy. paola.vittorioso@uniroma1.it.
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