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Improved binding site assignment by high-resolution mapping of RNA-protein interactions using iCLIP

Individual-nucleotide resolution crosslinking and immunoprecipitation (iCLIP) allows the determination of crosslinking sites of RNA-binding proteins (RBPs) on RNAs. iCLIP is based on ultraviolet light crosslinking of RBPs to RNA, reverse transcription and high-throughput sequencing of fragments term...

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Bibliographische Detailangaben
Hauptverfasser: Hauer, Christian (VerfasserIn) , Curk, Tomaz (VerfasserIn) , Anders, Simon (VerfasserIn) , Schwarzl, Thomas (VerfasserIn) , Alleaume, Anne-Marie (VerfasserIn) , Sieber, Jana (VerfasserIn) , Hollerer, Ina (VerfasserIn) , Bhuvanagiri, Madhuri (VerfasserIn) , Huber, Wolfgang (VerfasserIn) , Hentze, Matthias W. (VerfasserIn) , Kulozik, Andreas (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 11 Aug 2015
In: Nature Communications
Year: 2015, Jahrgang: 6
ISSN:2041-1723
DOI:10.1038/ncomms8921
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/ncomms8921
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/ncomms8921
Volltext
Verfasserangaben:Christian Hauer, Tomaz Curk, Simon Anders, Thomas Schwarzl, Anne-Marie Alleaume, Jana Sieber, Ina Hollerer, Madhuri Bhuvanagiri, Wolfgang Huber, Matthias W. Hentze, Andreas E. Kulozik
Beschreibung
Zusammenfassung:Individual-nucleotide resolution crosslinking and immunoprecipitation (iCLIP) allows the determination of crosslinking sites of RNA-binding proteins (RBPs) on RNAs. iCLIP is based on ultraviolet light crosslinking of RBPs to RNA, reverse transcription and high-throughput sequencing of fragments terminating at the site of crosslinking. As a result, start sites of iCLIP fragments are expected to cluster with a narrow distribution, typically representing the site of direct interaction between the RBP and the RNA. Here we show that for several RBPs (eIF4A3, PTB, SRSF3, SRSF4 and hnRNP L), the start sites of iCLIP fragments show a fragment length-dependent broader distribution that can be shifted to positions upstream of the known RNA-binding site. We developed an analysis tool that identifies these shifts and can improve the positioning of RBP binding sites.
Beschreibung:Gesehen am 14.07.2020
Beschreibung:Online Resource
ISSN:2041-1723
DOI:10.1038/ncomms8921

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