Detection of RNA–Protein Interactions in Living Cells with SHAPE

• Published in: Biochemistry (Easton) 2015-11, Vol.54 (46), p.6867-6875
• Main Authors: Smola, Matthew J, Calabrese, J. Mauro, Weeks, Kevin M
• Format: Article
• Language: English
• Subjects: Acylation; Animals; Binding Sites; Cells, Cultured; Embryonic Stem Cells - metabolism; Mice; Models, Molecular; Mutation; Nucleic Acid Conformation; phenotype; Protein Conformation; Proteins - chemistry; Proteins - metabolism; ribonucleases; ribonucleoproteins; Ribonucleoproteins - chemistry; Ribonucleoproteins - metabolism; RNA; RNA - chemistry; RNA - genetics; RNA - metabolism; stem cells; trophoblast; uncertainty
• ISSN: 0006-2960; 1520-4995; 1520-4995
• DOI: 10.1021/acs.biochem.5b00977

SHAPE-MaP is unique among RNA structure probing strategies in that it both measures flexibility at single-nucleotide resolution and quantifies the uncertainties in these measurements. We report a straightforward analytical framework that incorporates these uncertainties to allow detection of RNA structural differences between any two states, and we use it here to detect RNA–protein interactions in healthy mouse trophoblast stem cells. We validate this approach by analysis of three model cytoplasmic and nuclear ribonucleoprotein complexes, in 2 min in-cell probing experiments. In contrast, data produced by alternative in-cell SHAPE probing methods correlate poorly (r = 0.2) with those generated by SHAPE-MaP and do not yield accurate signals for RNA–protein interactions. We then examine RNA–protein and RNA–substrate interactions in the RNase MRP complex and, by comparing in-cell interaction sites with disease-associated mutations, characterize these noncoding mutations in terms of molecular phenotype. Together, these results reveal that SHAPE-MaP can define true interaction sites and infer RNA functions under native cellular conditions with limited preexisting knowledge of the proteins or RNAs involved.