Evidence map›Paper›PMID 24253111›Full record

ArticleRNA biology2013

Using RNA inverse folding to identify IRES-like structural subdomains.

Ivan Dotu, Gloria Lozano, Peter Clote, Encarnacion Martinez-Salas

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 21 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

4 authors at 2 institutions in 2 countries.

Ivan DotuBiology Department; Boston College; Chestnut Hill, MA USA.
Gloria LozanoCentro de Biologia Molecular Severo Ochoa; Consejo Superior de Investigaciones Cientificas-Universidad Autonoma de Madrid; Madrid, Spain.
Peter CloteBiology Department; Boston College; Chestnut Hill, MA USA.
Encarnacion Martinez-SalasCentro de Biologia Molecular Severo Ochoa; Consejo Superior de Investigaciones Cientificas-Universidad Autonoma de Madrid; Madrid, Spain.
Boston College · USCentro de Biología Molecular Severo Ochoa · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Internal ribosome entry site (IRES) elements govern protein synthesis of mRNAs that bypass cap-dependent translation inhibition under stress conditions. Picornavirus IRES are cis-acting elements, organized in modular domains that recruit the ribosome to internal mRNA sites. The aim of this study was to retrieve short RNA sequences with the capacity to adopt RNA folding patterns conserved with IRES structural subdomains, likely corresponding to RNA modules. We have applied a new program, RNAiFold, an inverse folding algorithm that determines all sequences whose minimum free energy structure is identical to that of the structural domains of interest. Sequences differing by more than 1 nt were clustered. Then, BLASTing one randomly chosen sequence from each cluster of the RNAiFold output, we retrieved viral and cellular sequences among output hits. As a proof of principle, we present the data corresponding to a coding region of Drosophila melanogaster TAF6, a transcription factor-associated protein that contains a structural motif within its coding region potentially folding into an IRES-like subdomain. This RNA region shows a biased codon usage, as predicted from structural constraints at the RNA level, it harbors conserved IRES structural motifs in loops, and interestingly, it has the capacity to confer internal initiation of translation in tissue culture cells.

Indexed as

AlgorithmsRegulatory Sequences, Ribonucleic AcidAnimalsDrosophila melanogasterDrosophila ProteinsGene Expression RegulationModels, MolecularNucleic Acid ConformationPicornaviridaeReproducibility of ResultsRibosomesRNA FoldingRNA, MessengerTATA-Binding Protein Associated FactorsTranscription Factor TFIIDDrosophila ProteinsRegulatory Sequences, Ribonucleic AcidRNA, MessengerTaf6 protein, DrosophilaTATA-Binding Protein Associated FactorsTranscription Factor TFIIDinverse foldingIRES elementsRNA structural domainsSHAPE analysistranslation control

Identifiers

PMID24253111
PMCPMC3917987
OpenAlexW2032187763

What OpenQuestion holds

Textmetadata
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.