PrismNet: predicting protein-RNA interaction using in vivo RNA structural information

Nucleic Acids Res. 2023 Jul 5;51(W1):W468-W477. doi: 10.1093/nar/gkad353.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Gene Expression Regulation
  • RNA* / chemistry
  • RNA-Binding Proteins* / metabolism

Substances

  • RNA
  • RNA-Binding Proteins

Associated data

  • figshare/10.6084/m9.figshare.22655101