Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783238384739680256 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5442315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT youyuan temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT sawikowskaaneta temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT neumannmanuela temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT posedavid temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT capovillagiovanna temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT langeneckertobias temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT neherricharda temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT krajewskipaweł temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering AT schmidmarkus temporaldynamicsofgeneexpressionandhistonemarksatthearabidopsisshootmeristemduringflowering |