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1Howard Hughes Medical Institute, Laboratory of RNA Molecular Biology,Rockefeller University, 2Berlin Institute for Medical Systems Biology,Max-Delbrück-Center for Molecular Medicine, 3Biozentrum der Universität Basel and Swiss Institute of Bioinformatics (SIB), 4Biozentrum der Universität Basel and Swiss Institute of Bioinformatics (SIB), 5Genomics Resource Center,Rockefeller University
Capitoli
- 00:00Titolo
- 00:53Introduction
- 01:27In vivo UV Crosslinking
- 04:06Immunoprecipitation of Protein
- 07:07Recovery of Crosslinked RNA-Protein Segments
- 10:19Representative PAR-CLiP Results
- 12:01Conclusion
RNA transcripts are subject to extensive posttranscriptional regulation that is mediated by a multitude of trans-acting RNA-binding proteins (RBPs). Here we present a generalizable method to identify precisely and on a transcriptome-wide scale the RNA binding sites of RBPs.
Tags
PAR-CliPTranscriptome-wideBinding SitesRNA-binding ProteinsPost-transcriptional Gene RegulationRNA TranscriptsRNA-RBP InteractionsMicroRNA-containing Ribonucleoprotein ComplexesCell-type DependentlyInterplayHigh Resolution MapsIn Vivo Protein-RNA InteractionsGenetic ApproachesBiochemical ApproachesComputational ApproachesMicroarray ProfilingRIP-ChipKinetically Stable InteractionsRBP Recognition Element (RRE)Direct RBP Target Site InformationUV CrosslinkingImmunoprecipitationCLIPUV 254 Nm RNA-protein Crosslinking
