Evidence map›Paper›PMID 22283730›Full record

ReviewNucleic acid therapeutics2012

Argonaute and the nuclear RNAs: new pathways for RNA-mediated control of gene expression.

Keith T Gagnon, David R Corey

Open access · hybridAbstract readReview
In one paragraph

Review in Nucleic acid therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. PSMC3 promotes RNAi by maintaining AGO2 stability through USP14.Cellular & molecular biology letters · 2022
    Article
  6. RNA binding proteins in MLL-rearranged leukemia.Experimental hematology & oncology · 2022
    Review
  7. Article
  8. Expression of tiRNA and tRF inAnnals of translational medicine · 2021
    Article
  9. MicroRNA 195-5p TargetsInternational journal of molecular sciences · 2021
    Article
  10. Article
  11. Action mechanisms and research methods of tRNA-derived small RNAs.Signal transduction and targeted therapy · 2020
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Epigenetic regulation of alternative splicing.American journal of cancer research · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

2 authors at 1 institution in 1 country.

Keith T GagnonDepartments of Pharmacology and Biochemistry, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390, USA.
David R Corey
Southwestern Medical Center

Funding

Recognition of Chromosomal DNA by Peptide Nucleic AcidsR01GM073042 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COREY, DAVID R · 2005 to 2016
$3.5M
Recognition of Chromosomal DNA by Double-Stranded RNAR01GM077253 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COREY, DAVID R · 2007 to 2010
$1.5M
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 1F32HD060377NIGMS NIH HHS GM73042NIGMS NIH HHS GM77253
6 · The paper itself

Abstract

Small RNAs are a commonly used tool for gene silencing and a promising platform for nucleic acid drug development. They are almost exclusively used to silence gene expression post-transcriptionally through degradation of mRNA. Small RNAs, however, can have a broader range of function by binding to Argonaute proteins and associating with complementary RNA targets in the nucleus, including long noncoding RNAs (lncRNAs) and pre-mRNA. Argonaute-RNA complexes can regulate nuclear events like transcription, genome maintenance, and splicing. Thousands of lncRNAs and alternatively spliced pre-mRNA isoforms exist in humans, and these RNAs may serve as natural targets for regulation and therapeutic intervention. This review describes nuclear mechanisms for Argonaute proteins and small RNAs, new pathways for sequence-specific targeting, and the potential for therapeutic development of small RNAs with nuclear targets.

Indexed as

AnimalsArgonaute ProteinsGene Expression RegulationHumansRNA InterferenceRNA, NuclearArgonaute ProteinsRNA, Nuclear

Identifiers

PMID22283730
PMCPMC3318256
OpenAlexW2158403894

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.