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Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions

Plants have a remarkable ability to react to seasonal changes by synchronizing life-cycle transitions with environmental conditions. We addressed the question of how transcriptional re-programming occurs in response to an environmental cue that triggers the major life cycle transition from seed dorm...

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Detalles Bibliográficos
Autores principales: Müller, Kerstin, Bouyer, Daniel, Schnittger, Arp, Kermode, Allison R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519861/
https://www.ncbi.nlm.nih.gov/pubmed/23240039
http://dx.doi.org/10.1371/journal.pone.0051532
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author Müller, Kerstin
Bouyer, Daniel
Schnittger, Arp
Kermode, Allison R.
author_facet Müller, Kerstin
Bouyer, Daniel
Schnittger, Arp
Kermode, Allison R.
author_sort Müller, Kerstin
collection PubMed
description Plants have a remarkable ability to react to seasonal changes by synchronizing life-cycle transitions with environmental conditions. We addressed the question of how transcriptional re-programming occurs in response to an environmental cue that triggers the major life cycle transition from seed dormancy to germination and seedling growth. We elucidated an important mechanistic aspect of this process by following the chromatin dynamics of key regulatory genes with a focus on the two antagonistic marks, H3K4me3 and H3K27me3. Histone methylation patterns of major dormancy regulators changed during the transition to germination and seedling growth. We observed a switch from H3K4me3 and high transcription levels to silencing by the repressive H3K27me3 mark when dormancy was broken through exposure to moist chilling, underscoring that a functional PRC2 complex is necessary for this transition. Moreover, this reciprocal regulation by H3K4me3 and H3K27me3 is evolutionarily conserved from gymnosperms to angiosperms.
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spelling pubmed-35198612012-12-13 Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions Müller, Kerstin Bouyer, Daniel Schnittger, Arp Kermode, Allison R. PLoS One Research Article Plants have a remarkable ability to react to seasonal changes by synchronizing life-cycle transitions with environmental conditions. We addressed the question of how transcriptional re-programming occurs in response to an environmental cue that triggers the major life cycle transition from seed dormancy to germination and seedling growth. We elucidated an important mechanistic aspect of this process by following the chromatin dynamics of key regulatory genes with a focus on the two antagonistic marks, H3K4me3 and H3K27me3. Histone methylation patterns of major dormancy regulators changed during the transition to germination and seedling growth. We observed a switch from H3K4me3 and high transcription levels to silencing by the repressive H3K27me3 mark when dormancy was broken through exposure to moist chilling, underscoring that a functional PRC2 complex is necessary for this transition. Moreover, this reciprocal regulation by H3K4me3 and H3K27me3 is evolutionarily conserved from gymnosperms to angiosperms. Public Library of Science 2012-12-11 /pmc/articles/PMC3519861/ /pubmed/23240039 http://dx.doi.org/10.1371/journal.pone.0051532 Text en © 2012 Müller et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Müller, Kerstin
Bouyer, Daniel
Schnittger, Arp
Kermode, Allison R.
Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title_full Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title_fullStr Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title_full_unstemmed Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title_short Evolutionarily Conserved Histone Methylation Dynamics during Seed Life-Cycle Transitions
title_sort evolutionarily conserved histone methylation dynamics during seed life-cycle transitions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519861/
https://www.ncbi.nlm.nih.gov/pubmed/23240039
http://dx.doi.org/10.1371/journal.pone.0051532
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