Evidence map›Paper›PMID 38956134›Full record

ArticleScientific reports2024

Comprehensive survey of conserved RNA secondary structures in full-genome alignment of Hepatitis C virus.

Sandra Triebel, Kevin Lamkiewicz, Nancy Ontiveros, Blake Sweeney, Peter F Stadler, Anton I Petrov, Michael Niepmann, Manja Marz

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Rfam 15: RNA families database in 2025.Nucleic acids research · 2025
    Article
  8. R2DT: A COMPREHENSIVE PLATFORM FOR VISUALISING RNA SECONDARY STRUCTURE.bioRxiv : the preprint server for biology · 2024
    Article
  9. Rfam 15: RNA families database in 2025.bioRxiv : the preprint server for biology · 2024
    Article
  10. 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

8 authors.

Sandra TriebelRNA Bioinformatics and High-Throughput Analysis, Friedrich Schiller University Jena, 07743, Jena, Germany.
Kevin LamkiewiczRNA Bioinformatics and High-Throughput Analysis, Friedrich Schiller University Jena, 07743, Jena, Germany.
Nancy OntiverosEuropean Molecular Biology Laboratory, Wellcome Genome Campus, European Bioinformatics Institute, Hinxton, Cambridge, CB10 1SD, UK.
Blake SweeneyEuropean Molecular Biology Laboratory, Wellcome Genome Campus, European Bioinformatics Institute, Hinxton, Cambridge, CB10 1SD, UK.
Peter F StadlerEuropean Virus Bioinformatics Center, Friedrich Schiller University Jena, 07743, Jena, Germany.ORCID 0000-0002-5016-5191
Anton I PetrovRiboscope Ltd., Cambridge, CB1 1AH, UK.
Michael NiepmannInstitute for Biochemistry, Justus-Liebig-University Giessen, 35392, Giessen, Germany.
Manja MarzRNA Bioinformatics and High-Throughput Analysis, Friedrich Schiller University Jena, 07743, Jena, Germany. manja@uni-jena.de.

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) EXC 2051-Project-ID 390713860Deutsche Forschungsgemeinschaft (German Research Foundation) FOR 5151 QuaLiPerF-TP4: MA5082/15-1Deutsche Forschungsgemeinschaft (German Research Foundation) SFB 1021-Project-ID 197785619EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) "VIROINF"-Project-ID 955974Thüringer Aufbaubank (TAB) Project-ID 2021 FGI 0009
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is a plus-stranded RNA virus that often chronically infects liver hepatocytes and causes liver cirrhosis and cancer. These viruses replicate their genomes employing error-prone replicases. Thereby, they routinely generate a large 'cloud' of RNA genomes (quasispecies) which-by trial and error-comprehensively explore the sequence space available for functional RNA genomes that maintain the ability for efficient replication and immune escape. In this context, it is important to identify which RNA secondary structures in the sequence space of the HCV genome are conserved, likely due to functional requirements. Here, we provide the first genome-wide multiple sequence alignment (MSA) with the prediction of RNA secondary structures throughout all representative full-length HCV genomes. We selected 57 representative genomes by clustering all complete HCV genomes from the BV-BRC database based on k-mer distributions and dimension reduction and adding RefSeq sequences. We include annotations of previously recognized features for easy comparison to other studies. Our results indicate that mainly the core coding region, the C-terminal NS5A region, and the NS5B region contain secondary structure elements that are conserved beyond coding sequence requirements, indicating functionality on the RNA level. In contrast, the genome regions in between contain less highly conserved structures. The results provide a complete description of all conserved RNA secondary structures and make clear that functionally important RNA secondary structures are present in certain HCV genome regions but are largely absent from other regions. Full-genome alignments of all branches of Hepacivirus C are provided in the supplement.

Indexed as

Conserved SequenceGenome, ViralHepacivirusNucleic Acid ConformationRNA, ViralHepatitis CHumansSequence AlignmentRNA, ViralFull-genome alignmentHepatitis C virusRNA secondary structure prediction

Identifiers

PMID38956134
PMCPMC11219754

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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.