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Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering

Plants can produce organs throughout their entire life from pluripotent stem cells located at their growing tip, the shoot apical meristem (SAM). At the time of flowering, the SAM of Arabidopsis thaliana switches fate and starts producing flowers instead of leaves. Correct timing of flowering in par...

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Autores principales: You, Yuan, Sawikowska, Aneta, Neumann, Manuela, Posé, David, Capovilla, Giovanna, Langenecker, Tobias, Neher, Richard A., Krajewski, Paweł, Schmid, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442315/
https://www.ncbi.nlm.nih.gov/pubmed/28513600
http://dx.doi.org/10.1038/ncomms15120
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author You, Yuan
Sawikowska, Aneta
Neumann, Manuela
Posé, David
Capovilla, Giovanna
Langenecker, Tobias
Neher, Richard A.
Krajewski, Paweł
Schmid, Markus
author_facet You, Yuan
Sawikowska, Aneta
Neumann, Manuela
Posé, David
Capovilla, Giovanna
Langenecker, Tobias
Neher, Richard A.
Krajewski, Paweł
Schmid, Markus
author_sort You, Yuan
collection PubMed
description Plants can produce organs throughout their entire life from pluripotent stem cells located at their growing tip, the shoot apical meristem (SAM). At the time of flowering, the SAM of Arabidopsis thaliana switches fate and starts producing flowers instead of leaves. Correct timing of flowering in part determines reproductive success, and is therefore under environmental and endogenous control. How epigenetic regulation contributes to the floral transition has eluded analysis so far, mostly because of the poor accessibility of the SAM. Here we report the temporal dynamics of the chromatin modifications H3K4me3 and H3K27me3 and their correlation with transcriptional changes at the SAM in response to photoperiod-induced flowering. Emphasizing the importance of tissue-specific epigenomic analyses we detect enrichments of chromatin states in the SAM that were not apparent in whole seedlings. Furthermore, our results suggest that regulation of translation might be involved in adjusting meristem function during the induction of flowering.
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spelling pubmed-54423152017-06-02 Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering You, Yuan Sawikowska, Aneta Neumann, Manuela Posé, David Capovilla, Giovanna Langenecker, Tobias Neher, Richard A. Krajewski, Paweł Schmid, Markus Nat Commun Article Plants can produce organs throughout their entire life from pluripotent stem cells located at their growing tip, the shoot apical meristem (SAM). At the time of flowering, the SAM of Arabidopsis thaliana switches fate and starts producing flowers instead of leaves. Correct timing of flowering in part determines reproductive success, and is therefore under environmental and endogenous control. How epigenetic regulation contributes to the floral transition has eluded analysis so far, mostly because of the poor accessibility of the SAM. Here we report the temporal dynamics of the chromatin modifications H3K4me3 and H3K27me3 and their correlation with transcriptional changes at the SAM in response to photoperiod-induced flowering. Emphasizing the importance of tissue-specific epigenomic analyses we detect enrichments of chromatin states in the SAM that were not apparent in whole seedlings. Furthermore, our results suggest that regulation of translation might be involved in adjusting meristem function during the induction of flowering. Nature Publishing Group 2017-05-17 /pmc/articles/PMC5442315/ /pubmed/28513600 http://dx.doi.org/10.1038/ncomms15120 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
You, Yuan
Sawikowska, Aneta
Neumann, Manuela
Posé, David
Capovilla, Giovanna
Langenecker, Tobias
Neher, Richard A.
Krajewski, Paweł
Schmid, Markus
Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title_full Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title_fullStr Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title_full_unstemmed Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title_short Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
title_sort temporal dynamics of gene expression and histone marks at the arabidopsis shoot meristem during flowering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442315/
https://www.ncbi.nlm.nih.gov/pubmed/28513600
http://dx.doi.org/10.1038/ncomms15120
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