Evidence map›Paper›PMID 24152551›Full record

ArticleRNA (New York, N.Y.)2013

SHAPE analysis of the 5' end of the Mason-Pfizer monkey virus (MPMV) genomic RNA reveals structural elements required for genome dimerization.

Suriya J Aktar, Ayesha Jabeen, Lizna M Ali, Valérie Vivet-Boudou, Roland Marquet, Tahir A Rizvi

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2013. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Suriya J Aktar
Ayesha Jabeen
Lizna M Ali
Valérie Vivet-Boudou
Roland Marquet
Tahir A Rizvi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Earlier genetic and structural prediction analyses revealed that the packaging determinants of Mason Pfizer monkey virus (MPMV) include two discontinuous core regions at the 5' end of its genomic RNA. RNA secondary structure predictions suggested that these packaging determinants fold into several stem-loops (SLs). To experimentally validate this structural model, we employed selective 2' hydroxyl acylation analyzed by primer extension (SHAPE), which examines the flexibility of the RNA backbone at each nucleotide position. Our SHAPE data validated several predicted structural motifs, including U5/Gag long-range interactions (LRIs), a stretch of single-stranded purine (ssPurine)-rich region, and a distinctive G-C-rich palindromic (pal) SL. Minimum free-energy structure predictions, phylogenetic, and in silico modeling analyses of different MPMV strains revealed that the U5 and gag sequences involved in the LRIs differ minimally within strains and maintain a very high degree of complementarity. Since the pal SL forms a helix loop containing a canonical "GC" dyad, it may act as a RNA dimerization initiation site (DIS), enabling the virus to package two copies of its genome. Analyses of wild-type and pal mutant RNAs revealed that disruption of pal sequence strongly affected RNA dimerization. However, when in vitro transcribed trans-complementary pal mutants were incubated together showed RNA dimerization was restored authenticating that the pal loop (5'-CGGCCG-3') functions as DIS.

Indexed as

DimerizationAcylationBase SequenceConserved SequenceDNA PrimersGenome, ViralInverted Repeat SequencesMason-Pfizer monkey virusModels, MolecularMolecular Sequence DataNucleic Acid ConformationRNA Splice SitesRNA, ViralThermodynamicsVirus AssemblyDNA PrimersRNA Splice SitesRNA, Viraldimerization initiation site (DIS)long-range interaction (LRI)Mason Pfizer monkey virus (MPMV)RNA dimerizationRNA packaging signal

Identifiers

PMID24152551
PMCPMC3884649

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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.