Evidence map›Paper›PMID 26787884›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Mobile small RNAs regulate genome-wide DNA methylation.

Mathew G Lewsey, Thomas J Hardcastle, Charles W Melnyk, Attila Molnar, Adrián Valli, Mark A Urich, Joseph R Nery, David C Baulcombe, Joseph R Ecker

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
67.8field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 231 citations in OpenAlex.

  1. Article
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  5. TheProceedings of the National Academy of Sciences of the United States of America · 2026
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  9. Article
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  13. RNA interference shapes stress responses inFrontiers in plant science · 2025
    Review
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  15. Article
  16. Article
  17. Article
  18. The plant siRNA landscape.The Plant cell · 2024
    Review
  19. Article
  20. Review

42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Mathew G LewseyGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037; Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037;
Thomas J HardcastleDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom;
Charles W MelnykDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom;
Attila MolnarDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom;
Adrián ValliDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom;
Mark A UrichGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037;
Joseph R NeryGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037;
David C BaulcombeDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom; dcb40@cam.ac.uk ecker@salk.edu.
Joseph R EckerGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037; Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037; Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, CA 92037 dcb40@cam.ac.uk ecker@salk.edu.
University of Cambridge · GBSalk Institute for Biological Studies · USHoward Hughes Medical Institute · US

Funding

European Research Council 340642
6 · The paper itself

Abstract

RNA silencing at the transcriptional and posttranscriptional levels regulates endogenous gene expression, controls invading transposable elements (TEs), and protects the cell against viruses. Key components of the mechanism are small RNAs (sRNAs) of 21-24 nt that guide the silencing machinery to their nucleic acid targets in a nucleotide sequence-specific manner. Transcriptional gene silencing is associated with 24-nt sRNAs and RNA-directed DNA methylation (RdDM) at cytosine residues in three DNA sequence contexts (CG, CHG, and CHH). We previously demonstrated that 24-nt sRNAs are mobile from shoot to root in Arabidopsis thaliana and confirmed that they mediate DNA methylation at three sites in recipient cells. In this study, we extend this finding by demonstrating that RdDM of thousands of loci in root tissues is dependent upon mobile sRNAs from the shoot and that mobile sRNA-dependent DNA methylation occurs predominantly in non-CG contexts. Mobile sRNA-dependent non-CG methylation is largely dependent on the DOMAINS REARRANGED METHYLTRANSFERASES 1/2 (DRM1/DRM2) RdDM pathway but is independent of the CHROMOMETHYLASE (CMT)2/3 DNA methyltransferases. Specific superfamilies of TEs, including those typically found in gene-rich euchromatic regions, lose DNA methylation in a mutant lacking 22- to 24-nt sRNAs (dicer-like 2, 3, 4 triple mutant). Transcriptome analyses identified a small number of genes whose expression in roots is associated with mobile sRNAs and connected to DNA methylation directly or indirectly. Finally, we demonstrate that sRNAs from shoots of one accession move across a graft union and target DNA methylation de novo at normally unmethylated sites in the genomes of root cells from a different accession.

Indexed as

Genome, PlantAllelesArabidopsisDNA MethylationDNA Transposable ElementsGene Expression Regulation, PlantGenetic LociPlant RootsRNA, PlantDNA Transposable ElementsRNA, Plantplant graftingRNA-directed DNA methylationsmall RNAtranscriptional gene silencingtransposable element

Identifiers

PMID26787884
PMCPMC4760824
OpenAlexW2225514865

What OpenQuestion holds

Textmetadata
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.