Abstract
Fundamental to post-Transcriptional regulation, the in vivo binding of RNA binding proteins (RBPs) on their RNA targets heavily depends on RNA structures. To date, most methods for RBP-RNA interaction prediction are based on RNA structures predicted from sequences, which do not consider the various intracellular environments and thus cannot predict cell type-specific RBP-RNA interactions. Here, we present a web server PrismNet that uses a deep learning tool to integrate in vivo RNA secondary structures measured by icSHAPE experiments with RBP binding site information from UV cross-linking and immunoprecipitation in the same cell lines to predict cell type-specific RBP-RNA interactions. Taking an RBP and an RNA region with sequential and structural information as input ('Sequence & Structure' mode), PrismNet outputs the binding probability of the RBP and this RNA region, together with a saliency map and a sequence-structure integrative motif. The web server is freely available at http://prismnetweb.zhanglab.net.
Cite
CITATION STYLE
Xu, Y., Zhu, J., Huang, W., Xu, K., Yang, R., Zhang, Q. C., & Sun, L. (2023). PrismNet: Predicting protein-RNA interaction using in vivo RNA structural information. Nucleic Acids Research, 51(W1), W468–W477. https://doi.org/10.1093/nar/gkad353
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