Evidence map›Paper›PMID 26524240›Full record

ArticleNature methods2015

Protein-RNA networks revealed through covalent RNA marks.

Christopher P Lapointe, Daniel Wilinski, Harriet A J Saunders, Marvin Wickens

Abstract read
In one paragraph

Article in Nature methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

60 citing papers in PubMed, 97 citations in OpenAlex.

  1. Probing RNA-protein interactions in the early mouse embryo.bioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Article
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  5. Review
  6. Article
  7. Review
  8. CRISPR/Cas13 sgRNA-Mediated RNA-RNA Interaction Mapping in Live Cells with APOBEC RNA Editing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
  10. Mapping subcellular RNA localization with proximity labeling.Acta biochimica et biophysica Sinica · 2024
    Review
  11. Article
  12. Article
  13. Current progress in strategies to profile transcriptomic mFrontiers in cell and developmental biology · 2024
    Review
  14. RNA binding proteins in cardiovascular development and disease.Current topics in developmental biology · 2024
    Article
  15. Article
  16. Review
  17. Identification of RNA-Binding Protein Targets with HyperTRIBE inInternational journal of molecular sciences · 2023
    Article
  18. Role of the RNA-binding protein family in gynecologic cancers.American journal of cancer research · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Christopher P LapointeDepartment of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Daniel WilinskiDepartment of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Harriet A J SaundersDepartment of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Marvin WickensDepartment of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
University of Wisconsin–Madison · US

Funding

FUNCTION OF POLY(A) AND 3'UTRSR01GM050942 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI WICKENS, MARVIN P. · 1994 to 2020
$8.3M
NIGMS NIH HHS GM50942NIGMS NIH HHS R01 GM050942
6 · The paper itself

Abstract

Protein-RNA networks are ubiquitous and central in biological control. We present an approach termed RNA Tagging that enables the user to identify protein-RNA interactions in vivo by analyzing purified cellular RNA, without protein purification or cross-linking. An RNA-binding protein of interest is fused to an enzyme that adds uridines to the end of RNA. RNA targets bound by the chimeric protein in vivo are covalently marked with uridines and subsequently identified from extracted RNA via high-throughput sequencing. We used this approach to identify hundreds of RNAs bound by a Saccharomyces cerevisiae PUF protein, Puf3p. The results showed that although RNA-binding proteins productively bind specific RNAs to control their function, they also 'sample' RNAs without exerting a regulatory effect. We used the method to uncover hundreds of new and likely regulated targets for a protein without canonical RNA-binding domains, Bfr1p. RNA Tagging is well suited to detect and analyze protein-RNA networks in vivo.

Indexed as

3' Untranslated RegionsBinding SitesProtein BindingRepressor ProteinsRNA-Binding ProteinsRNA, FungalRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae Proteins3' Untranslated RegionsBFR1 protein, S cerevisiaePUF3 protein, S cerevisiaeRepressor ProteinsRNA-Binding ProteinsRNA, FungalRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID26524240
PMCPMC4707952
OpenAlexW1921157559

What OpenQuestion holds

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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.