Evidence map›Paper›PMID 19834549›Full record

ArticlePLoS pathogens2009

Probing the HIV-1 genomic RNA trafficking pathway and dimerization by genetic recombination and single virion analyses.

Michael D Moore, Olga A Nikolaitchik, Jianbo Chen, Marie-Louise Hammarskjöld, David Rekosh, Wei-Shau Hu

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

77 citing papers in PubMed, 99 citations in OpenAlex.

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17 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Michael D MooreHIV Drug Resistance Program, National Cancer Institute, Frederick, MD, USA.
Olga A Nikolaitchik
Jianbo Chen
Marie-Louise Hammarskjöld
David Rekosh
Wei-Shau Hu
Frederick National Laboratory for Cancer Research · USNational Cancer Institute · USUniversity of Virginia · US

Funding

Understanding the Pseudodiploidy of the Retroviral GenomeZIABC010814 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HU, WEI-SHAU · 2009 to 2025
$12.3M
Understanding Retroviral Reverse Transcription, Recombination, and ReplicationZIABC010504 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HU, WEI-SHAU · 2009 to 2025
$5.3M
Sam 68 and the Function of Mason Pfizer Monkey Virus CTER01CA097095 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HAMMARSKJOLD, MARIE-LOUISE · 2003 to 2007
$1.5M
Compounds That Inhibit HIV Rev FunctionR01AI068501 · NIAID · UNIVERSITY OF VIRGINIA · PI REKOSH, DAVID M · 2006 to 2008
$1.3M
Understanding the Pseudodiploidy of the Retroviral GenomeZ01BC010814 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HU, WEI-SHAU · 2007 to 2008
$819k
Intramural NIH HHS Z01 BC010814NCI NIH HHS CA097095NCI NIH HHS R01 CA097095NIAID NIH HHS AI068501NIAID NIH HHS R01 AI068501
6 · The paper itself

Abstract

Once transcribed, the nascent full-length RNA of HIV-1 must travel to the appropriate host cell sites to be translated or to find a partner RNA for copackaging to form newly generated viruses. In this report, we sought to delineate the location where HIV-1 RNA initiates dimerization and the influence of the RNA transport pathway used by the virus on downstream events essential to viral replication. Using a cell-fusion-dependent recombination assay, we demonstrate that the two RNAs destined for copackaging into the same virion select each other mostly within the cytoplasm. Moreover, by manipulating the RNA export element in the viral genome, we show that the export pathway taken is important for the ability of RNA molecules derived from two viruses to interact and be copackaged. These results further illustrate that at the point of dimerization the two main cellular export pathways are partially distinct. Lastly, by providing Gag in trans, we have demonstrated that Gag is able to package RNA from either export pathway, irrespective of the transport pathway used by the gag mRNA. These findings provide unique insights into the process of RNA export in general, and more specifically, of HIV-1 genomic RNA trafficking.

Indexed as

HIV-1Molecular Probe TechniquesRecombination, GeneticActive Transport, Cell NucleusBiological TransportCell NucleusCells, CulturedDimerizationgag Gene Products, Human Immunodeficiency VirusGenome, ViralHumansModels, BiologicalRNA, ViralSignal TransductionVirionVirus Assemblygag Gene Products, Human Immunodeficiency VirusRNA, Viral

Identifiers

PMID19834549
PMCPMC2757677
OpenAlexW2003181803

What OpenQuestion holds

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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.