Evidence map›Paper›PMID 25349403›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Functional conservation despite structural divergence in ligand-responsive RNA switches.

Mark A Boerneke, Sergey M Dibrov, Jing Gu, David L Wyles, Thomas Hermann

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Target-Directed Approaches for Screening Small Molecules against RNA Targets.SLAS discovery : advancing life sciences R & D · 2020
    Review
  12. Review
  13. The Role of the RNA-RNA Interactome in the Hepatitis C Virus Life Cycle.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Pervasive tertiary structure in the dengue virus RNA genome.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. Dynamics of IRES-mediated translation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
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 2 institutions in 1 country.

Mark A BoernekeDepartment of Chemistry and Biochemistry.
Sergey M DibrovDepartment of Chemistry and Biochemistry.
Jing GuDepartment of Chemistry and Biochemistry.
David L WylesDivision of Infectious Diseases, Department of Medicine, and.
Thomas HermannDepartment of Chemistry and Biochemistry, Center for Drug Discovery Innovation, University of California, San Diego, La Jolla, CA 92093 tch@ucsd.edu.
Office of Infectious Diseases · USUniversity of California, San Diego · US

Funding

VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUSAN JANET LITTLE · 1994 to 2026
$78.4M
X-ray generator and associated optics for macromolecular crystallography at UCSDS10OD011957 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PARTHO · 2012 to 2012
$398k
NIAID NIH HHS P30 AI036214NIH HHS OD011957NIH HHS S10 OD011957
6 · The paper itself

Abstract

An internal ribosome entry site (IRES) initiates protein synthesis in RNA viruses, including the hepatitis C virus (HCV). We have discovered ligand-responsive conformational switches in viral IRES elements. Modular RNA motifs of greatly distinct sequence and local secondary structure have been found to serve as functionally conserved switches involved in viral IRES-driven translation and may be captured by identical cognate ligands. The RNA motifs described here constitute a new paradigm for ligand-captured switches that differ from metabolite-sensing riboswitches with regard to their small size, as well as the intrinsic stability and structural definition of the constitutive conformational states. These viral RNA modules represent the simplest form of ligand-responsive mechanical switches in nucleic acids.

Indexed as

Nucleic Acid ConformationRegulatory Sequences, Ribonucleic AcidCell-Free SystemHepacivirusProtein BiosynthesisRNA, ViralViral ProteinsRegulatory Sequences, Ribonucleic AcidRNA, ViralViral Proteinshepatitis C virusIRES elementsRNA virusestranslation regulation

Identifiers

PMID25349403
PMCPMC4234586
OpenAlexW2105902657

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.