Evidence map›Paper›PMID 31511048›Full record

ArticleEpigenetics & chromatin2019

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

Adéla Přibylová, Vojtěch Čermák, Dimitrij Tyč, Lukáš Fischer

Open access · goldAbstract read
In one paragraph

Article in Epigenetics & chromatin, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  7. Barley somatic embryogenesis-an attempt to modify variation induced in tissue culture.Journal of biological research (Thessalonike, Greece) · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Adéla PřibylováDepartment of Experimental Plant Biology, Charles University, Faculty of Science, 128 44, Prague, Czech Republic.ORCID 0000-0001-8675-5065
Vojtěch ČermákDepartment of Experimental Plant Biology, Charles University, Faculty of Science, 128 44, Prague, Czech Republic.
Dimitrij TyčDepartment of Experimental Plant Biology, Charles University, Faculty of Science, 128 44, Prague, Czech Republic.
Lukáš FischerDepartment of Experimental Plant Biology, Charles University, Faculty of Science, 128 44, Prague, Czech Republic. lukasf@natur.cuni.cz.ORCID 0000-0003-1852-0461
Charles University · CZ

Funding

Ministry of Education, Youth and Sports of the Czech Republic LO1417
6 · The paper itself

Abstract

backgroundMethylation 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.

resultsWe 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.

conclusionsOur 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.

Indexed as

DNA MethylationCaulimovirusEstradiolGreen Fluorescent ProteinsNicotianaPlant CellsPlasmidsPromoter Regions, GeneticRNA InterferenceRNA, Small InterferingEstradiolGreen Fluorescent ProteinsRNA, Small InterferingEpigeneticsRdDMRNA interferencesRNA sequencingTranscriptional gene silencing

Identifiers

PMID31511048
PMCPMC6737654
OpenAlexW2972419973

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.