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CLIP and complementary methods

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TLDR
The prospect of integrating data obtained by CLIP with complementary methods to gain a comprehensive view of RNP assembly and remodelling, unravel the spatial and temporal dynamics of RNPs in specific cell types and subcellular compartments and understand how defects in RNPs can lead to disease are discussed.
Abstract
RNA molecules start assembling into ribonucleoprotein (RNP) complexes during transcription. Dynamic RNP assembly, largely directed by cis-acting elements on the RNA, coordinates all processes in which the RNA is involved. To identify the sites bound by a specific RNA-binding protein on endogenous RNAs, cross-linking and immunoprecipitation (CLIP) and complementary, proximity-based methods have been developed. In this Primer, we discuss the main variants of these protein-centric methods and the strategies for their optimization and quality assessment, as well as RNA-centric methods that identify the protein partners of a specific RNA. We summarize the main challenges of computational CLIP data analysis, how to handle various sources of background and how to identify functionally relevant binding regions. We outline the various applications of CLIP and available databases for data sharing. We discuss the prospect of integrating data obtained by CLIP with complementary methods to gain a comprehensive view of RNP assembly and remodelling, unravel the spatial and temporal dynamics of RNPs in specific cell types and subcellular compartments and understand how defects in RNPs can lead to disease. Finally, we present open questions in the field and give directions for further development and applications. Ule and colleagues discuss cross-linking and immunoprecipitation (CLIP) methods for characterizing the RNA binding partners of RNA-binding proteins and explore the data analysis workflows, best practices and applications for these techniques. The Primer also considers methods for characterizing the protein binding partners of specific RNAs and discusses how data from these complementary methods can be integrated into CLIP workflows.

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References
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Journal ArticleDOI

Current approaches for RNA-labelling to identify RNA-binding proteins

TL;DR: A collection of methods for modifying RNA to capture RNA-binding proteins are reviewed, including small-molecule modification, the addition of aptamers, DNA-anchoring, and nucleotide substitution.
Posted ContentDOI

Systematic discovery and functional interrogation of SARS-CoV-2 viral RNA-host protein interactions during infection

TL;DR: A comprehensive catalogue of SARS-CoV-2 RNA-host protein interactions is provided, which may inform future studies to understand the mechanisms of viral pathogenesis, as well as nominate host pathways that could be targeted for therapeutic benefit.
Journal ArticleDOI

RNA-Centric Methods: Toward the Interactome of Specific RNA Transcripts

TL;DR: An overview of methods to identify RNA-protein interactions can be found in this article, with a particular focus on strategies that provide insights into the interactome of specific RNA transcripts, including the potential of CRISPR-RNA targeting systems to investigate endogenous RNA−protein interactions.
Journal ArticleDOI

SpyCLIP: an easy-to-use and high-throughput compatible CLIP platform for the characterization of protein–RNA interactions with high accuracy

TL;DR: A SpyCLIP method is reported that employs a covalent linkage formed between the RBP-fused SpyTag and SpyCatcher, which can withstand the harshest washing conditions for removing nonspecific interactions and provides a robust method for both routine characterization and high-throughput studies of protein–RNA interactions.
Journal ArticleDOI

CLIP and RNA interactome studies to unravel genome-wide RNA-protein interactions in vivo in Arabidopsis thaliana.

TL;DR: Practical considerations on the application of UV irradiation based methods to comprehensively determine in vivo RNA-protein interactions in Arabidopsis thaliana are presented, focussing on individual nucleotide resolution crosslinking immunoprecipitation (iCLIP) and mRNA interactome capture.
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