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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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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. |
format | Online Article Text |
id | pubmed-3519861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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