Evidence map›Paper›PMID 26696443›Full record

ArticlePLoS biology2015

Plants Encode a General siRNA Suppressor That Is Induced and Suppressed by Viruses.

Nahid Shamandi, Matthias Zytnicki, Cyril Charbonnel, Emilie Elvira-Matelot, Aurore Bochnakian, Pascale Comella, Allison C Mallory, Gersende Lepère, Julio Sáez-Vásquez, Hervé Vaucheret

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
9.3field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 51 citations in OpenAlex.

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  15. Redox Components: Key Regulators of Epigenetic Modifications in Plants.International journal of molecular sciences · 2020
    Review
  16. RNA silencing ofBiotechnology reports (Amsterdam, Netherlands) · 2019
    Article
  17. Article
  18. Plant Responses to Pathogen Attack: Small RNAs in Focus.International journal of molecular sciences · 2018
    Review
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 1 country.

Nahid ShamandiInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Matthias ZytnickiURGI, INRA, Versailles, France.
Cyril CharbonnelCNRS, UMR 5096, LGDP, Perpignan, France.
Emilie Elvira-MatelotInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Aurore BochnakianInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Pascale ComellaCNRS, UMR 5096, LGDP, Perpignan, France.
Allison C MalloryInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Gersende LepèreInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Julio Sáez-VásquezCNRS, UMR 5096, LGDP, Perpignan, France.
Hervé VaucheretInstitut Jean-Pierre Bourgin, UMR 1318, INRA AgroParisTech CNRS, Université Paris-Saclay, Versailles, France.
Centre National de la Recherche Scientifique · FRInstitut Jean-Pierre Bourgin · FRUniversité de Perpignan · FRAgroParisTech · FRUniversité Paris-Saclay · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small RNAs play essential regulatory roles in genome stability, development, and responses to biotic and abiotic stresses in most eukaryotes. In plants, the RNaseIII enzyme DICER-LIKE1 (DCL1) produces miRNAs, whereas DCL2, DCL3, and DCL4 produce various size classes of siRNAs. Plants also encode RNASE THREE-LIKE (RTL) enzymes that lack DCL-specific domains and whose function is largely unknown. We found that virus infection induces RTL1 expression, suggesting that this enzyme could play a role in plant-virus interaction. To first investigate the biochemical activity of RTL1 independent of virus infection, small RNAs were sequenced from transgenic plants constitutively expressing RTL1. These plants lacked almost all DCL2-, DCL3-, and DCL4-dependent small RNAs, indicating that RTL1 is a general suppressor of plant siRNA pathways. In vivo and in vitro assays revealed that RTL1 prevents siRNA production by cleaving dsRNA prior to DCL2-, DCL3-, and DCL4-processing. The substrate of RTL1 cleavage is likely long-perfect (or near-perfect) dsRNA, consistent with the RTL1-insensitivity of miRNAs, which derive from DCL1-processing of short-imperfect dsRNA. Virus infection induces RTL1 mRNA accumulation, but viral proteins that suppress RNA silencing inhibit RTL1 activity, suggesting that RTL1 has evolved as an inducible antiviral defense that could target dsRNA intermediates of viral replication, but that a broad range of viruses counteract RTL1 using the same protein toolbox used to inhibit antiviral RNA silencing. Together, these results reveal yet another level of complexity in the evolutionary battle between viruses and plant defenses.

Indexed as

Gene Expression Regulation, PlantHost-Pathogen InteractionsAmino Acid SubstitutionArabidopsisArabidopsis ProteinsCarmovirusComputational BiologyCucumovirusIsoenzymesMutagenesis, Site-DirectedMutant ProteinsPlants, Genetically ModifiedPoint MutationRecombinant Fusion ProteinsRepressor ProteinsRNA, MessengerArabidopsis ProteinsIsoenzymesMutant ProteinsRecombinant Fusion ProteinsRepressor ProteinsRNA, MessengerRNA, PlantRNA, Small InterferingRTL1 protein, Arabidopsis

Identifiers

PMID26696443
PMCPMC4687873
OpenAlexW2216633015

What OpenQuestion holds

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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.