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A computational platform for high-throughput analysis of RNA sequences and modifications by mass spectrometry.
Wein, Samuel; Andrews, Byron; Sachsenberg, Timo; Santos-Rosa, Helena; Kohlbacher, Oliver; Kouzarides, Tony; Garcia, Benjamin A; Weisser, Hendrik.
Afiliación
  • Wein S; Epigenetics Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Andrews B; Center for Bioinformatics Tübingen, University of Tübingen, Tübingen, Germany.
  • Sachsenberg T; STORM Therapeutics Limited, Moneta Building, Babraham Research Campus, Cambridge, UK.
  • Santos-Rosa H; Applied Bioinformatics, Department for Computer Science, University of Tübingen, Tübingen, Germany.
  • Kohlbacher O; Gurdon Institute, University of Cambridge, Cambridge, UK.
  • Kouzarides T; Center for Bioinformatics Tübingen, University of Tübingen, Tübingen, Germany.
  • Garcia BA; Applied Bioinformatics, Department for Computer Science, University of Tübingen, Tübingen, Germany.
  • Weisser H; Quantitative Biology Center, University of Tübingen, Tübingen, Germany.
Nat Commun ; 11(1): 926, 2020 02 17.
Article en En | MEDLINE | ID: mdl-32066737
ABSTRACT
The field of epitranscriptomics continues to reveal how post-transcriptional modification of RNA affects a wide variety of biological phenomena. A pivotal challenge in this area is the identification of modified RNA residues within their sequence contexts. Mass spectrometry (MS) offers a comprehensive solution by using analogous approaches to shotgun proteomics. However, software support for the analysis of RNA MS data is inadequate at present and does not allow high-throughput processing. Existing software solutions lack the raw performance and statistical grounding to efficiently handle the numerous modifications found on RNA. We present a free and open-source database search engine for RNA MS data, called NucleicAcidSearchEngine (NASE), that addresses these shortcomings. We demonstrate the capability of NASE to reliably identify a wide range of modified RNA sequences in four original datasets of varying complexity. In human tRNA, we characterize over 20 different modification types simultaneously and find many cases of incomplete modification.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Procesamiento Postranscripcional del ARN / Espectrometría de Masas en Tándem / Ensayos Analíticos de Alto Rendimiento / Motor de Búsqueda / Epigenómica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Procesamiento Postranscripcional del ARN / Espectrometría de Masas en Tándem / Ensayos Analíticos de Alto Rendimiento / Motor de Búsqueda / Epigenómica Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos