Evidence map›Paper›PMID 19106143›Full record

ArticleNucleic acids research2009

The A-rich RNA sequences of HIV-1 pol are important for the synthesis of viral cDNA.

Cameron P Keating, Melissa K Hill, David J Hawkes, Redmond P Smyth, Catherine Isel, Shu-Yun Le, Ann C Palmenberg, John A Marshall, Roland Marquet, Gary J Nabel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  6. Biased Mutation and Selection in RNA Viruses.Molecular biology and evolution · 2021
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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

11 authors at 5 institutions in 4 countries.

Cameron P KeatingCentre for Virology, Macfarlane Burnet Institute for Medical Research and Public Health, Melbourne, Victoria, Australia.
Melissa K Hill
David J Hawkes
Redmond P Smyth
Catherine Isel
Shu-Yun Le
Ann C Palmenberg
John A Marshall
Roland Marquet
Gary J Nabel
Johnson Mak
Architecture et Réactivité de l'arN · FRBurnet Institute · AUCenter for Cancer Research · USInstitute of Virology of the Slovak Academy of Sciences · SKVictorian Infectious Diseases Reference Laboratory · AU

Funding

Intramural NIH HHS
6 · The paper itself

Abstract

The bias of A-rich codons in HIV-1 pol is thought to be a record of hypermutations in viral genomes that lack biological functions. Bioinformatic analysis predicted that A-rich sequences are generally associated with minimal local RNA structures. Using codon modifications to reduce the amount of A-rich sequences within HIV-1 genomes, we have reduced the flexibility of RNA sequences in pol to analyze the functional significance of these A-rich 'structurally poor' RNA elements in HIV-1 pol. Our data showed that codon modification of HIV-1 sequences led to a suppression of virus infectivity by 5-100-fold, and this defect does not correlate with, viral entry, viral protein expression levels, viral protein profiles or virion packaging of genomic RNA. Codon modification of HIV-1 pol correlated with an enhanced dimer stability of the viral RNA genome, which was associated with a reduction of viral cDNA synthesis both during HIV-1 infection and in a cell free reverse transcription assay. Our data provided direct evidence that the HIV-1 A-rich pol sequence is not merely an evolutionary artifact of enzyme-induced hypermutations, and that HIV-1 has adapted to rely on A-rich RNA sequences to support the synthesis of viral cDNA during reverse transcription, highlighting the utility of using 'structurally poor' RNA domains in regulating biological process.

Indexed as

Genes, polRegulatory Sequences, Ribonucleic AcidReverse TranscriptionAdenineBase SequenceCell LineCodonDimerizationDNA, ComplementaryDNA, ViralHIV-1HumansNucleic Acid ConformationRNA, ViralViral ProteinsVirionAdenineCodonDNA, ComplementaryDNA, ViralRegulatory Sequences, Ribonucleic AcidRNA, ViralViral Proteins

Identifiers

PMID19106143
PMCPMC2647285
OpenAlexW2056947125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.