Evidence map›Paper›PMID 23028332›Full record

ArticlePLoS pathogens2012

Primary and secondary siRNAs in geminivirus-induced gene silencing.

Michael Aregger, Basanta K Borah, Jonathan Seguin, Rajendran Rajeswaran, Ekaterina G Gubaeva, Anna S Zvereva, David Windels, Franck Vazquez, Todd Blevins, Laurent Farinelli and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
16.5field-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

80 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Geminivirus diseases of legumes in India: current status and approaches for management.Physiology and molecular biology of plants : an international journal of functional plant biology · 2025
    Review
  6. Article
  7. Review
  8. The plant siRNA landscape.The Plant cell · 2024
    Review
  9. Article
  10. Article
  11. Infection Defects of RNA and DNA Viruses Induced by Antiviral RNA Interference.Microbiology and molecular biology reviews : MMBR · 2023
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. The master role of siRNAs in plant immunity.Molecular plant pathology · 2022
    Review
  20. PepYLCIV and PepYLCAV resistance gene Pepy-2 encodes DFDGD-Class RNA-dependent RNA polymerase in Capsicum.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2022
    Article

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

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

11 authors at 2 institutions in 2 countries.

Michael AreggerInstitute of Botany, University of Basel, Basel, Switzerland.
Basanta K Borah
Jonathan Seguin
Rajendran Rajeswaran
Ekaterina G Gubaeva
Anna S Zvereva
David Windels
Franck Vazquez
Todd Blevins
Laurent Farinelli
Mikhail M Pooggin
University of Basel · CHIndiana University Bloomington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In plants, RNA silencing-based antiviral defense is mediated by Dicer-like (DCL) proteins producing short interfering (si)RNAs. In Arabidopsis infected with the bipartite circular DNA geminivirus Cabbage leaf curl virus (CaLCuV), four distinct DCLs produce 21, 22 and 24 nt viral siRNAs. Using deep sequencing and blot hybridization, we found that viral siRNAs of each size-class densely cover the entire viral genome sequences in both polarities, but highly abundant siRNAs correspond primarily to the leftward and rightward transcription units. Double-stranded RNA precursors of viral siRNAs can potentially be generated by host RDR-dependent RNA polymerase (RDR). However, genetic evidence revealed that CaLCuV siRNA biogenesis does not require RDR1, RDR2, or RDR6. By contrast, CaLCuV derivatives engineered to target 30 nt sequences of a GFP transgene by primary viral siRNAs trigger RDR6-dependent production of secondary siRNAs. Viral siRNAs targeting upstream of the GFP stop codon induce secondary siRNAs almost exclusively from sequences downstream of the target site. Conversely, viral siRNAs targeting the GFP 3'-untranslated region (UTR) induce secondary siRNAs mostly upstream of the target site. RDR6-dependent siRNA production is not necessary for robust GFP silencing, except when viral siRNAs targeted GFP 5'-UTR. Furthermore, viral siRNAs targeting the transgene enhancer region cause GFP silencing without secondary siRNA production. We conclude that the majority of viral siRNAs accumulating during geminiviral infection are RDR1/2/6-independent primary siRNAs. Double-stranded RNA precursors of these siRNAs are likely generated by bidirectional readthrough transcription of circular viral DNA by RNA polymerase II. Unlike transgenic mRNA, geminiviral mRNAs appear to be poor templates for RDR-dependent production of secondary siRNAs.

Indexed as

RNA Interference3' Untranslated Regions5' Untranslated RegionsArabidopsisArabidopsis ProteinsGeminiviridaeGene Expression Regulation, PlantGreen Fluorescent ProteinsHigh-Throughput Nucleotide SequencingPlant DiseasesRNA-Dependent RNA PolymeraseRNA, Double-StrandedRNA Polymerase IIRNA, Small InterferingRNA, Viral3' Untranslated Regions5' Untranslated RegionsArabidopsis ProteinsGreen Fluorescent ProteinsRDR2 protein, ArabidopsisRDR6 protein, ArabidopsisRNA-Dependent RNA PolymeraseRNA, Double-StrandedRNA Polymerase IIRNA, Small InterferingRNA, Viral

Identifiers

PMID23028332
PMCPMC3460622
OpenAlexW1963719858

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.