Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature
Chromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-...
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doaj-980ab619ad394e6385c804693173c3a72020-11-24T21:42:20ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2020-02-011110.3389/fpls.2020.00039494585Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low TemperatureKora Vyse0Léa Faivre1Melissa Romich2Majken Pagter3Daniel Schubert4Dirk K. Hincha5Ellen Zuther6Central Infrastructure Group Genomics and Transcript Profiling, Max-Planck-Institute of Molecular Plant Physiology, Potsdam, GermanyInstitute of Biology, Freie Universität Berlin, Berlin, GermanyInstitute of Biology, Freie Universität Berlin, Berlin, GermanyDepartment of Chemistry and Bioscience, Aalborg University, Aalborg East, DenmarkInstitute of Biology, Freie Universität Berlin, Berlin, GermanyCentral Infrastructure Group Genomics and Transcript Profiling, Max-Planck-Institute of Molecular Plant Physiology, Potsdam, GermanyCentral Infrastructure Group Genomics and Transcript Profiling, Max-Planck-Institute of Molecular Plant Physiology, Potsdam, GermanyChromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-transcriptional level upon stress exposure and relief from stress. We reveal that the repressive modification histone H3 lysine 27 trimethylation (H3K27me3) targets genes which are quickly activated upon cold exposure, however, H3K27me3 is not necessarily lost during a longer time in the cold. In addition, we have set-up a quantitative reverse transcription polymerase chain reaction-based platform for high-throughput transcriptional profiling of a large set of chromatin genes. We find that the expression of many of these genes is regulated by cold. In addition, we reveal an induction of several DNA and histone demethylase genes and certain histone variants after plants have been shifted back to ambient temperature (deacclimation), suggesting a role in the memory of cold acclimation. We also re-analyze large scale transcriptomic datasets for transcriptional regulation and alternative splicing (AS) of chromatin genes, uncovering an unexpected level of regulation of these genes, particularly at the splicing level. This includes several vernalization regulating genes whose AS may result in cold-regulated protein diversity. Overall, we provide a profiling platform for the analysis of chromatin regulatory genes and integrative analyses of their regulation, suggesting a dynamic regulation of key chromatin genes in response to low temperature stress.https://www.frontiersin.org/article/10.3389/fpls.2020.00039/fullchromatin regulatorsquantitative reverse transcription polymerase chain reaction platformhistonescold acclimationdeacclimation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kora Vyse Léa Faivre Melissa Romich Majken Pagter Daniel Schubert Dirk K. Hincha Ellen Zuther |
spellingShingle |
Kora Vyse Léa Faivre Melissa Romich Majken Pagter Daniel Schubert Dirk K. Hincha Ellen Zuther Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature Frontiers in Plant Science chromatin regulators quantitative reverse transcription polymerase chain reaction platform histones cold acclimation deacclimation |
author_facet |
Kora Vyse Léa Faivre Melissa Romich Majken Pagter Daniel Schubert Dirk K. Hincha Ellen Zuther |
author_sort |
Kora Vyse |
title |
Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature |
title_short |
Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature |
title_full |
Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature |
title_fullStr |
Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature |
title_full_unstemmed |
Transcriptional and Post-Transcriptional Regulation and Transcriptional Memory of Chromatin Regulators in Response to Low Temperature |
title_sort |
transcriptional and post-transcriptional regulation and transcriptional memory of chromatin regulators in response to low temperature |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Plant Science |
issn |
1664-462X |
publishDate |
2020-02-01 |
description |
Chromatin regulation ensures stable repression of stress-inducible genes under non-stress conditions and transcriptional activation and memory of stress-related genes after stress exposure. However, there is only limited knowledge on how chromatin genes are regulated at the transcriptional and post-transcriptional level upon stress exposure and relief from stress. We reveal that the repressive modification histone H3 lysine 27 trimethylation (H3K27me3) targets genes which are quickly activated upon cold exposure, however, H3K27me3 is not necessarily lost during a longer time in the cold. In addition, we have set-up a quantitative reverse transcription polymerase chain reaction-based platform for high-throughput transcriptional profiling of a large set of chromatin genes. We find that the expression of many of these genes is regulated by cold. In addition, we reveal an induction of several DNA and histone demethylase genes and certain histone variants after plants have been shifted back to ambient temperature (deacclimation), suggesting a role in the memory of cold acclimation. We also re-analyze large scale transcriptomic datasets for transcriptional regulation and alternative splicing (AS) of chromatin genes, uncovering an unexpected level of regulation of these genes, particularly at the splicing level. This includes several vernalization regulating genes whose AS may result in cold-regulated protein diversity. Overall, we provide a profiling platform for the analysis of chromatin regulatory genes and integrative analyses of their regulation, suggesting a dynamic regulation of key chromatin genes in response to low temperature stress. |
topic |
chromatin regulators quantitative reverse transcription polymerase chain reaction platform histones cold acclimation deacclimation |
url |
https://www.frontiersin.org/article/10.3389/fpls.2020.00039/full |
work_keys_str_mv |
AT koravyse transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT leafaivre transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT melissaromich transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT majkenpagter transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT danielschubert transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT dirkkhincha transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature AT ellenzuther transcriptionalandposttranscriptionalregulationandtranscriptionalmemoryofchromatinregulatorsinresponsetolowtemperature |
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