Evidence map›Paper›PMID 36453997›Full record

ArticleNucleic acids research2022

Deciphering RNA G-quadruplex function during the early steps of HIV-1 infection.

Samir Amrane, Chloé Jaubert, Amina Bedrat, Tiffany Rundstadler, Patricia Recordon-Pinson, Cindy Aknin, Aurore Guédin, Aurore De Rache, Laura Bartolucci, Ibra Diene and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Samir AmraneUniversité de Bordeaux, Bordeaux, France.ORCID 0000-0003-0147-776X
Chloé JaubertUniversité de Bordeaux, Bordeaux, France.
Amina BedratUniversité de Bordeaux, Bordeaux, France.
Tiffany RundstadlerUniversité de Toulouse, UPS, INPT, Toulouse, France.
Patricia Recordon-PinsonUniversité de Bordeaux, Bordeaux, France.
Cindy AkninUniversité de Bordeaux, Bordeaux, France.
Aurore GuédinUniversité de Bordeaux, Bordeaux, France.
Aurore De RacheUniversité de Bordeaux, Bordeaux, France.
Laura BartolucciUniversité de Bordeaux, Bordeaux, France.
Ibra DieneUniversité de Bordeaux, Bordeaux, France.
Frédéric LemoineInstitut Pasteur, Université de Paris, Unité de Bioinformatique Évolutive, F-75015 Paris, France.ORCID 0000-0001-9576-4449
Olivier GascuelInstitut Pasteur, Université de Paris, Unité de Bioinformatique Évolutive, F-75015 Paris, France.
Geneviève PratvielUniversité de Toulouse, UPS, INPT, Toulouse, France.
Jean-Louis MergnyUniversité de Bordeaux, Bordeaux, France.ORCID 0000-0003-3043-8401
Marie-Line AndreolaUniversité de Bordeaux, Bordeaux, France.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G-quadruplexes (G4s) are four-stranded nucleic acid structures formed by the stacking of G-tetrads. Here we investigated their formation and function during HIV-1 infection. Using bioinformatics and biophysics analyses we first searched for evolutionary conserved G4-forming sequences in HIV-1 genome. We identified 10 G4s with conservation rates higher than those of HIV-1 regulatory sequences such as RRE and TAR. We then used porphyrin-based G4-binders to probe the formation of the G4s during infection of human cells by native HIV-1. The G4-binders efficiently inhibited HIV-1 infectivity, which is attributed to the formation of G4 structures during HIV-1 replication. Using a qRT-PCR approach, we showed that the formation of viral G4s occurs during the first 2 h post-infection and their stabilization by the G4-binders prevents initiation of reverse transcription. We also used a G4-RNA pull-down approach, based on a G4-specific biotinylated probe, to allow the direct detection and identification of viral G4-RNA in infected cells. Most of the detected G4-RNAs contain crucial regulatory elements such as the PPT and cPPT sequences as well as the U3 region. Hence, these G4s would function in the early stages of infection when the viral RNA genome is being processed for the reverse transcription step.

Indexed as

G-QuadruplexesHIV-1Conserved SequenceHumansRegulatory Sequences, Nucleic AcidRNARNA

Identifiers

PMID36453997
PMCPMC9757044
OpenAlexW4310381596

What OpenQuestion holds

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LicenceCC BY-NC
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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.