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A high-throughput approach to profile RNA structure

Identifieur interne : 001013 ( Main/Exploration ); précédent : 001012; suivant : 001014

A high-throughput approach to profile RNA structure

Auteurs : Riccardo Delli Ponti [Espagne] ; Stefanie Marti [Espagne] ; Alexandros Armaos [Espagne] ; Gian Gaetano Tartaglia [Espagne]

Source :

RBID : PMC:5389523

Abstract

Abstract

Here we introduce the Computational Recognition of Secondary Structure (CROSS) method to calculate the structural profile of an RNA sequence (single- or double-stranded state) at single-nucleotide resolution and without sequence length restrictions. We trained CROSS using data from high-throughput experiments such as Selective 2΄-Hydroxyl Acylation analyzed by Primer Extension (SHAPE; Mouse and HIV transcriptomes) and Parallel Analysis of RNA Structure (PARS; Human and Yeast transcriptomes) as well as high-quality NMR/X-ray structures (PDB database). The algorithm uses primary structure information alone to predict experimental structural profiles with >80% accuracy, showing high performances on large RNAs such as Xist (17 900 nucleotides; Area Under the ROC Curve AUC of 0.75 on dimethyl sulfate (DMS) experiments). We integrated CROSS in thermodynamics-based methods to predict secondary structure and observed an increase in their predictive power by up to 30%.


Url:
DOI: 10.1093/nar/gkw1094
PubMed: 27899588
PubMed Central: 5389523


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Here we introduce the Computational Recognition of Secondary Structure (CROSS) method to calculate the structural profile of an RNA sequence (single- or double-stranded state) at single-nucleotide resolution and without sequence length restrictions. We trained CROSS using data from high-throughput experiments such as Selective 2΄-Hydroxyl Acylation analyzed by Primer Extension (SHAPE; Mouse and HIV transcriptomes) and Parallel Analysis of RNA Structure (PARS; Human and Yeast transcriptomes) as well as high-quality NMR/X-ray structures (PDB database). The algorithm uses primary structure information alone to predict experimental structural profiles with >80% accuracy, showing high performances on large RNAs such as
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</back>
</TEI>
<affiliations>
<list>
<country>
<li>Espagne</li>
</country>
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<li>Catalogne</li>
</region>
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<li>Barcelone</li>
</settlement>
<orgName>
<li>Université Pompeu Fabra</li>
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</list>
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<name sortKey="Delli Ponti, Riccardo" sort="Delli Ponti, Riccardo" uniqKey="Delli Ponti R" first="Riccardo" last="Delli Ponti">Riccardo Delli Ponti</name>
<name sortKey="Marti, Stefanie" sort="Marti, Stefanie" uniqKey="Marti S" first="Stefanie" last="Marti">Stefanie Marti</name>
<name sortKey="Marti, Stefanie" sort="Marti, Stefanie" uniqKey="Marti S" first="Stefanie" last="Marti">Stefanie Marti</name>
<name sortKey="Tartaglia, Gian Gaetano" sort="Tartaglia, Gian Gaetano" uniqKey="Tartaglia G" first="Gian Gaetano" last="Tartaglia">Gian Gaetano Tartaglia</name>
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<name sortKey="Tartaglia, Gian Gaetano" sort="Tartaglia, Gian Gaetano" uniqKey="Tartaglia G" first="Gian Gaetano" last="Tartaglia">Gian Gaetano Tartaglia</name>
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</record>

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