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Analysis of CLIP and iCLIP methods for nucleotide-resolution studies of protein-RNA interactions | Genome Biology
Description:
UV cross-linking and immunoprecipitation (CLIP) and individual-nucleotide resolution CLIP (iCLIP) are methods to study protein-RNA interactions in untreated cells and tissues. Here, we analyzed six published and two novel data sets to confirm that both methods identify protein-RNA cross-link sites, and to identify a slight uridine preference of UV-C-induced cross-linking. Comparing Nova CLIP and iCLIP data revealed that cDNA deletions have a preference for TTT motifs, whereas iCLIP cDNA truncations are more likely to identify clusters of YCAY motifs as the primary Nova binding sites. In conclusion, we demonstrate how each method impacts the analysis of protein-RNA binding specificity.
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Keywords {🔍}
iclip, sites, cdna, clip, cdnas, deletions, crosslink, nova, ycay, pubmed, rna, figure, motifs, article, deletion, position, crosslinking, binding, google, scholar, motif, enrichment, analysis, truncations, file, cas, additional, data, proportion, sequence, ttt, nucleotide, identify, central, score, methods, proteins, identified, nsun, genome, compared, site, darnell, truncated, readthrough, studies, protein, positions, proteinrna, splicing,
Topics {✒️}
false discovery rate uv-c-induced cross-linking uv-c-induced cross-linking [22] perform uv-independent cross-linking protein-rna cross-link sites article number r67 article download pdf par-clip requires pre-incubation nova-dependent splicing enhancer nova-dependent splicing regulation nova splicing-regulatory network genome-wide rna maps identify protein-rna interactions protein-rna cross-linking uv-induced cross-linking nop2/sun domain family cross-link sites induced photoactivatable ribonucleoside-enhanced clip cross-linking predominantly occurs hyper-variable ca microsatellite article sugimoto cross-link sites influence spontaneous covalent cross-linking nova k-homology domains covalent cross-linking protocols identify cross-link sites position-dependent splicing regulation cross-link sites identified cross-link induced mutations cross-link-induced mutations kh rna-binding domains protein-rna binding specificity sequence-specific rna binding study protein-rna interactions 1186/gb-2009-10-3-r25 mapping rna-protein interactions full-length nova proteins understand post-transcriptional regulation vivo protein-rna interactions identifying cross-link sites cross-linking bias accession number e-mtab-1008 individual-nucleotide resolution clip alternative splicing regulation author information authors cross-link site identification cross-link sites starting high-affinity binding sites isolate rnas cross-linked julian könig & jernej ule
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headline:Analysis of CLIP and iCLIP methods for nucleotide-resolution studies of protein-RNA interactions
description:UV cross-linking and immunoprecipitation (CLIP) and individual-nucleotide resolution CLIP (iCLIP) are methods to study protein-RNA interactions in untreated cells and tissues. Here, we analyzed six published and two novel data sets to confirm that both methods identify protein-RNA cross-link sites, and to identify a slight uridine preference of UV-C-induced cross-linking. Comparing Nova CLIP and iCLIP data revealed that cDNA deletions have a preference for TTT motifs, whereas iCLIP cDNA truncations are more likely to identify clusters of YCAY motifs as the primary Nova binding sites. In conclusion, we demonstrate how each method impacts the analysis of protein-RNA binding specificity.
datePublished:2012-08-03T00:00:00Z
dateModified:2012-08-03T00:00:00Z
pageStart:1
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license:http://creativecommons.org/licenses/by/2.0/
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keywords:
Sequence Bias
False Discovery Rate Threshold
Deletion Site
cDNA Truncation
Nova Protein
Animal Genetics and Genomics
Human Genetics
Plant Genetics and Genomics
Microbial Genetics and Genomics
Bioinformatics
Evolutionary Biology
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headline:Analysis of CLIP and iCLIP methods for nucleotide-resolution studies of protein-RNA interactions
description:UV cross-linking and immunoprecipitation (CLIP) and individual-nucleotide resolution CLIP (iCLIP) are methods to study protein-RNA interactions in untreated cells and tissues. Here, we analyzed six published and two novel data sets to confirm that both methods identify protein-RNA cross-link sites, and to identify a slight uridine preference of UV-C-induced cross-linking. Comparing Nova CLIP and iCLIP data revealed that cDNA deletions have a preference for TTT motifs, whereas iCLIP cDNA truncations are more likely to identify clusters of YCAY motifs as the primary Nova binding sites. In conclusion, we demonstrate how each method impacts the analysis of protein-RNA binding specificity.
datePublished:2012-08-03T00:00:00Z
dateModified:2012-08-03T00:00:00Z
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keywords:
Sequence Bias
False Discovery Rate Threshold
Deletion Site
cDNA Truncation
Nova Protein
Animal Genetics and Genomics
Human Genetics
Plant Genetics and Genomics
Microbial Genetics and Genomics
Bioinformatics
Evolutionary Biology
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Analytics and Tracking {📊}
- Google Tag Manager
Libraries {📚}
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CDN Services {📦}
- Crossref