학술논문

GCLiPP: global crosslinking and protein purification method for constructing high-resolution occupancy maps for RNA binding proteins
Document Type
article
Source
Genome Biology. 24(1)
Subject
Biological Sciences
Bioinformatics and Computational Biology
Biotechnology
Human Genome
Genetics
1.1 Normal biological development and functioning
Underpinning research
Generic health relevance
Animals
Humans
Mice
RNA-Binding Proteins
Binding Sites
Transcriptome
RNA
Protein Binding
Immunoprecipitation
Post-transcriptional regulation
RNA-binding proteins
T cells
Cis-regulatory elements
Environmental Sciences
Information and Computing Sciences
Bioinformatics
Language
Abstract
GCLiPP is a global RNA interactome capture method that detects RNA-binding protein (RBP) occupancy transcriptome-wide. GCLiPP maps RBP-occupied sites at a higher resolution than phase separation-based techniques. GCLiPP sequence tags correspond with known RBP binding sites and are enriched for sites detected by RBP-specific crosslinking immunoprecipitation (CLIP) for abundant cytosolic RBPs. Comparison of human Jurkat T cells and mouse primary T cells uncovers shared peaks of GCLiPP signal across homologous regions of human and mouse 3' UTRs, including a conserved mRNA-destabilizing cis-regulatory element. GCLiPP signal overlapping with immune-related SNPs uncovers stabilizing cis-regulatory regions in CD5, STAT6, and IKZF1.