Evidence map›Paper›PMID 39747944›Full record

ArticleScientific reports2025

Asymmetric distribution of G-quadruplex forming sequences in genomes of retroviruses.

Filip Kledus, Michaela Dobrovolná, Jean-Louis Mergny, Václav Brázda

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Filip KledusInstitute of Biophysics , Czech Academy of Sciences , Královopolská 135, Brno, 612 65, Czech Republic.
Michaela DobrovolnáInstitute of Biophysics , Czech Academy of Sciences , Královopolská 135, Brno, 612 65, Czech Republic.
Jean-Louis MergnyInstitute of Biophysics , Czech Academy of Sciences , Královopolská 135, Brno, 612 65, Czech Republic.
Václav BrázdaInstitute of Biophysics , Czech Academy of Sciences , Královopolská 135, Brno, 612 65, Czech Republic. vaclav@ibp.cz.

Funding

Fondation de l'Ecole Polytechnique 2023 - PathogensGrantová Agentura České Republiky 22-21903SINTERREG AT-CZ ATCZ0052
6 · The paper itself

Abstract

Retroviruses are among the most extensively studied viral families, both historically and in contemporary research. They are primarily investigated in the fields of viral oncogenesis, reverse transcription mechanisms, and other infection-specific aspects. These include the integration of endogenous retroviruses (ERVs) into host genomes, a process widely utilized in genetic engineering, and the ongoing search for HIV/AIDS treatment. G-quadruplexes (G4) have emerged as potential therapeutic targets in antiviral therapy and have been identified in important regulatory regions of viral genomes. In this study, we examine the presence of potential G-quadruplex-forming sequences (PQS) across all currently available unique retroviral genomes. Given that these retroviral genomes typically consist of single-stranded RNA (ssRNA) molecules, we also investigated whether the localization of PQSs is strand-dependent. This is particularly relevant since antisense transcripts have been detected in HIV, and ERV integration into the host genome involves reverse transcription from genomic positive strand ssRNA to double-stranded DNA (dsDNA), implicating both strands in this process. We show that in most mammalian retroviruses, including human retroviruses, PQSs are significantly more prevalent on the negative (antisense) strand, with some notable exceptions such as HIV-1. In sharp contrast, avian retroviruses exhibit a higher prevalence of PQSs on the positive (sense) strand.

Indexed as

Genome, ViralG-QuadruplexesRetroviridaeAnimalsEndogenous RetrovirusesHumansBioinformaticsG4HunterG-quadruplexPersistent infectionRetroviral genome

Identifiers

PMID39747944
PMCPMC11696869

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Registered trials

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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.