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Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells

BACKGROUND: Methylation of cytosines is an evolutionarily conserved epigenetic mark that is essential for the control of chromatin activity in many taxa. It acts mainly repressively, causing transcriptional gene silencing. In plants, de novo DNA methylation is established mainly by RNA-directed DNA-...

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Autores principales: Přibylová, Adéla, Čermák, Vojtěch, Tyč, Dimitrij, Fischer, Lukáš
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737654/
https://www.ncbi.nlm.nih.gov/pubmed/31511048
http://dx.doi.org/10.1186/s13072-019-0299-0
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author Přibylová, Adéla
Čermák, Vojtěch
Tyč, Dimitrij
Fischer, Lukáš
author_facet Přibylová, Adéla
Čermák, Vojtěch
Tyč, Dimitrij
Fischer, Lukáš
author_sort Přibylová, Adéla
collection PubMed
description BACKGROUND: Methylation of cytosines is an evolutionarily conserved epigenetic mark that is essential for the control of chromatin activity in many taxa. It acts mainly repressively, causing transcriptional gene silencing. In plants, de novo DNA methylation is established mainly by RNA-directed DNA-methylation pathway. Even though the protein machinery involved is relatively well-described, the course of the initial phases remains covert. RESULTS: We show the first detailed description of de novo DNA-methylation dynamics. Since prevalent plant model systems do not provide the possibility to collect homogenously responding material in time series with short intervals, we developed a convenient system based on tobacco BY-2 cell lines with inducible production of siRNAs (from an RNA hairpin) guiding the methylation machinery to the CaMV 35S promoter controlling GFP reporter. These lines responded very synchronously, and a high level of promoter-specific siRNAs triggered rapid promoter methylation with the first increase observed already 12 h after the induction. The previous presence of CG methylation in the promoter did not affect the methylation dynamics. The individual cytosine contexts reacted differently. CHH methylation peaked at about 80% in 2 days and then declined, whereas CG and CHG methylation needed more time with CHG reaching practically 100% after 10 days. Spreading of methylation was only minimal outside the target region in accordance with the absence of transitive siRNAs. The low and stable proportion of 24-nt siRNAs suggested that Pol IV was not involved in the initial phases. CONCLUSIONS: Our results show that de novo DNA methylation is a rapid process initiated practically immediately with the appearance of promoter-specific siRNAs and independently of the prior presence of methylcytosines at the target locus. The methylation was precisely targeted, and its dynamics varied depending on the cytosine sequence context. The progressively increasing methylation resulted in a smooth, gradual inhibition of the promoter activity, which was entirely suppressed in 2 days.
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spelling pubmed-67376542019-09-16 Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells Přibylová, Adéla Čermák, Vojtěch Tyč, Dimitrij Fischer, Lukáš Epigenetics Chromatin Research BACKGROUND: Methylation of cytosines is an evolutionarily conserved epigenetic mark that is essential for the control of chromatin activity in many taxa. It acts mainly repressively, causing transcriptional gene silencing. In plants, de novo DNA methylation is established mainly by RNA-directed DNA-methylation pathway. Even though the protein machinery involved is relatively well-described, the course of the initial phases remains covert. RESULTS: We show the first detailed description of de novo DNA-methylation dynamics. Since prevalent plant model systems do not provide the possibility to collect homogenously responding material in time series with short intervals, we developed a convenient system based on tobacco BY-2 cell lines with inducible production of siRNAs (from an RNA hairpin) guiding the methylation machinery to the CaMV 35S promoter controlling GFP reporter. These lines responded very synchronously, and a high level of promoter-specific siRNAs triggered rapid promoter methylation with the first increase observed already 12 h after the induction. The previous presence of CG methylation in the promoter did not affect the methylation dynamics. The individual cytosine contexts reacted differently. CHH methylation peaked at about 80% in 2 days and then declined, whereas CG and CHG methylation needed more time with CHG reaching practically 100% after 10 days. Spreading of methylation was only minimal outside the target region in accordance with the absence of transitive siRNAs. The low and stable proportion of 24-nt siRNAs suggested that Pol IV was not involved in the initial phases. CONCLUSIONS: Our results show that de novo DNA methylation is a rapid process initiated practically immediately with the appearance of promoter-specific siRNAs and independently of the prior presence of methylcytosines at the target locus. The methylation was precisely targeted, and its dynamics varied depending on the cytosine sequence context. The progressively increasing methylation resulted in a smooth, gradual inhibition of the promoter activity, which was entirely suppressed in 2 days. BioMed Central 2019-09-11 /pmc/articles/PMC6737654/ /pubmed/31511048 http://dx.doi.org/10.1186/s13072-019-0299-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Přibylová, Adéla
Čermák, Vojtěch
Tyč, Dimitrij
Fischer, Lukáš
Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title_full Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title_fullStr Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title_full_unstemmed Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title_short Detailed insight into the dynamics of the initial phases of de novo RNA-directed DNA methylation in plant cells
title_sort detailed insight into the dynamics of the initial phases of de novo rna-directed dna methylation in plant cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737654/
https://www.ncbi.nlm.nih.gov/pubmed/31511048
http://dx.doi.org/10.1186/s13072-019-0299-0
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