Evidence map›Paper›PMID 22179787›Full record

ArticleNature structural & molecular biology2011

Tudor domain ERI-5 tethers an RNA-dependent RNA polymerase to DCR-1 to potentiate endo-RNAi.

Caroline Thivierge, Neetha Makil, Mathieu Flamand, Jessica J Vasale, Craig C Mello, James Wohlschlegel, Darryl Conte, Thomas F Duchaine

Erratum issuedAbstract read
In one paragraph

Article in Nature structural & molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
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

49 citing papers in PubMed.

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  15. eLife · 2024
    Article
  16. bioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Biogenesis ofScience advances · 2022
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors.

Caroline ThiviergeDepartment of Biochemistry, McGill University, Montreal, Quebec, Canada.
Neetha Makil
Mathieu Flamand
Jessica J Vasale
Craig C Mello
James Wohlschlegel
Darryl Conte
Thomas F Duchaine

Funding

Proteolytic Control of Iron Metabolism by the Ubiquitin Ligase FBXL5R01GM089778 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WOHLSCHLEGEL, JAMES AKIRA · 2010 to 2023
$4.0M
CIHR MOP 86577Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM089778
6 · The paper itself

Abstract

Endogenous RNA interference (endo-RNAi) pathways use a variety of mechanisms to generate siRNA and to mediate gene silencing. In Caenorhabditis elegans, DCR-1 is essential for competing RNAi pathways-the ERI endo-RNAi pathway and the exogenous RNAi pathway-to function. Here, we demonstrate that DCR-1 forms exclusive complexes in each pathway and further define the ERI-DCR-1 complex. We show that the tandem tudor protein ERI-5 potentiates ERI endo-RNAi by tethering an RNA-dependent RNA polymerase (RdRP) module to DCR-1. In the absence of ERI-5, the RdRP module is uncoupled from DCR-1. Notably, EKL-1, an ERI-5 paralog that specifies distinct RdRP modules in Dicer-independent endo-RNAi pathways, partially compensates for the loss of ERI-5 without interacting with DCR-1. Our results implicate tudor proteins in the recruitment of RdRP complexes to specific steps within DCR-1-dependent and DCR-1-independent endo-RNAi pathways.

Indexed as

RNA InterferenceAnimalsBlotting, WesternCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsEmbryo, NonmammalianImmunoprecipitationMutationProtein BindingRecombinant ProteinsRibonuclease IIIRNA-Dependent RNA PolymeraseRNA-Induced Silencing ComplexRNA, Small InterferingCaenorhabditis elegans ProteinsCarrier Proteinsdcr-1 protein, C elegansERI-5 protein, C elegansRecombinant ProteinsRibonuclease IIIRNA-Dependent RNA PolymeraseRNA-Induced Silencing ComplexRNA, Small Interfering

Identifiers

PMID22179787
PMCPMC3684169

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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.