GCLiPP: global crosslinking and protein purification method for constructing high-resolution occupancy maps for RNA binding proteins.
Wandi S ZhuAdam J LittermanHarshaan S SekhonRobin KageyamaMaya M ArceKimberly E TaylorWenxue ZhaoLindsey A CriswellNoah ZaitlenDavid J ErleKarl Mark AnselPublished in: Genome biology (2023)
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.
Keyphrases
- binding protein
- endothelial cells
- high resolution
- transcription factor
- induced pluripotent stem cells
- genome wide
- acute lymphoblastic leukemia
- dna damage
- gene expression
- pluripotent stem cells
- cell proliferation
- mass spectrometry
- nucleic acid
- single molecule
- single cell
- small molecule
- rna seq
- protein protein
- tandem mass spectrometry
- recombinant human
- genome wide association