Evidence map›Paper›PMID 26476446›Full record

ArticleNucleic acids research2015

Full-length RNA structure prediction of the HIV-1 genome reveals a conserved core domain.

Zsuzsanna Sükösd, Ebbe S Andersen, Stefan E Seemann, Mads Krogh Jensen, Mathias Hansen, Jan Gorodkin, Jørgen Kjems

Abstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  6. Article
  7. Article
  8. RNA structure inference through chemical mapping after accidental or intentional mutations.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  9. Virus evolution · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Bridging the gap between in vitro and in vivo RNA folding.Quarterly reviews of biophysics · 2016
    Article
  14. 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

7 authors.

Zsuzsanna SükösdBiRC, Bioinformatics Research Centre, Aarhus University, DK-8000 Aarhus C, Denmark zsuzsanna.etches@qiagen.com.
Ebbe S AnderseniNANO, Interdisciplinary Nanoscience Center, Aarhus University, DK-8000 Aarhus C, Denmark.
Stefan E SeemannRTH, Center for non-coding RNA in Technology and Health, Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, DK-1870 Frederiksberg C, Denmark.
Mads Krogh JensenBiRC, Bioinformatics Research Centre, Aarhus University, DK-8000 Aarhus C, Denmark.
Mathias HansenBiRC, Bioinformatics Research Centre, Aarhus University, DK-8000 Aarhus C, Denmark.
Jan GorodkinRTH, Center for non-coding RNA in Technology and Health, Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, DK-1870 Frederiksberg C, Denmark.
Jørgen KjemsiNANO, Interdisciplinary Nanoscience Center, Aarhus University, DK-8000 Aarhus C, Denmark jk@mb.au.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A distance constrained secondary structural model of the ≈10 kb RNA genome of the HIV-1 has been predicted but higher-order structures, involving long distance interactions, are currently unknown. We present the first global RNA secondary structure model for the HIV-1 genome, which integrates both comparative structure analysis and information from experimental data in a full-length prediction without distance constraints. Besides recovering known structural elements, we predict several novel structural elements that are conserved in HIV-1 evolution. Our results also indicate that the structure of the HIV-1 genome is highly variable in most regions, with a limited number of stable and conserved RNA secondary structures. Most interesting, a set of long distance interactions form a core organizing structure (COS) that organize the genome into three major structural domains. Despite overlapping protein-coding regions the COS is supported by a particular high frequency of compensatory base changes, suggesting functional importance for this element. This new structural element potentially organizes the whole genome into three major domains protruding from a conserved core structure with potential roles in replication and evolution for the virus.

Indexed as

Genome, ViralHIV-1Models, GeneticNucleic Acid ConformationRNA, ViralSoftwareRNA, Viral

Identifiers

PMID26476446
PMCPMC4666355

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LicenceCC BY
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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.