Evidence map›Paper›PMID 24388755›Full record

ArticleCell reports2014

RNAi factors are present and active in human cell nuclei.

Keith T Gagnon, Liande Li, Yongjun Chu, Bethany A Janowski, David R Corey

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 241 papers.

0numbers the graph read from it
0cells of the map it votes in
241citing papers in PubMed
18.6field-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

241 citing papers in PubMed, 371 citations in OpenAlex.

  1. Lentiviral RNAi for Depletion of Enhancer RNAs in Primary Neurons.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. RNA therapeutics: current status and future directions.Signal transduction and targeted therapy · 2026
    Review
  3. Delpacibart etedesiran improves the molecular pathology of myotonic dystrophy type 1 in the phase 1/2 MARINA study.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  8. Development of an AAV-delivered microRNA gene therapy for myotonic dystrophy type 1.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  9. Article
  10. Unlocking the role of tRNA-derived fragments in shaping breast cancer signaling.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
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  13. Article
  14. Review
  15. Review
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181 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

5 authors at 1 institution in 1 country.

Keith T GagnonDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9041, USA.
Liande LiDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9041, USA.
Yongjun ChuDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9041, USA.
Bethany A JanowskiDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9041, USA.
David R CoreyDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9041, USA. Electronic address: david.corey@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

Recognition of Chromosomal DNA by Peptide Nucleic AcidsR01GM073042 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COREY, DAVID R · 2005 to 2016
$3.5M
Molecular Switches: Regulatory RNAs Targeting Nuclear Hormone Receptor PromotersR01GM085080 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI JANOWSKI, BETHANY ANN · 2009 to 2013
$1.2M
Activating Gene Expression with Antigene RNAs to Treat Genetic DiseasesF32HD060377 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI GAGNON, KEITH THOMAS · 2009 to 2012
$152k
NICHD NIH HHS 1F32HD060377NICHD NIH HHS F32 HD060377NIGMS NIH HHS GM 73042NIGMS NIH HHS GM85080NIGMS NIH HHS R01 GM073042NIGMS NIH HHS R01 GM085080
6 · The paper itself

Abstract

RNAi is widely appreciated as a powerful regulator of mRNA translation in the cytoplasm of mammalian cells. However, the presence and activity of RNAi factors in the mammalian nucleus has been the subject of considerable debate. Here, we show that Argonaute-2 (Ago2) and RNAi factors Dicer, TRBP, and TRNC6A/GW182 are in the human nucleus and associate together in multiprotein complexes. Small RNAs can silence nuclear RNA and guide site-specific cleavage of the targeted RNA, demonstrating that RNAi can function in the human nucleus. Nuclear Dicer is active and miRNAs are bound to nuclear Ago2, consistent with the existence of nuclear miRNA pathways. Notably, we do not detect loading of duplex small RNAs in nuclear extracts and known loading factors are absent. These results extend RNAi into the mammalian nucleus and suggest that regulation of RNAi via small RNA loading of Ago2 differs between the cytoplasm and the nucleus.

Indexed as

RNA InterferenceArgonaute ProteinsAutoantigensCell NucleusCytoplasmDEAD-box RNA HelicasesHeLa CellsHumansProtein BindingRibonuclease IIIRNA-Binding ProteinsTrans-Activation Responsive RNA-Binding ProteinAGO2 protein, humanArgonaute ProteinsAutoantigensDEAD-box RNA HelicasesDICER1 protein, humanRibonuclease IIIRNA-Binding ProteinsTNRC6A protein, humanTrans-Activation Responsive RNA-Binding Protein

Identifiers

PMID24388755
PMCPMC3916906
OpenAlexW2003931886

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.