bioRxivBiochemistryPreprint
Decoding RNA-RNA Interactions: The Role of Low-Complexity Repeats and a Deep Learning Framework for Sequence-Based Prediction
Adriano SettiiD, Giorgio Bini, Flaminia PellegriniiD, Valentino MaiorcaiD, Gabriele Proietti, Dimitrios Miltiadis VrachnosiD, Angelo D’AngeloiD, Alexandros ArmaosiD, Julie MartoneiD, Michele M. MontiiD, Giancarlo RuoccoiD, Emanuele RodolàiD, Irene BozzoniiD, Alessio ColantoniiD, Gian Gaetano TartagliaiD
- Citations
- 2
Abstract
RNA-RNA interactions (RRIs) are fundamental to gene regulation and RNA processing, yet their molecular determinants remain unclear. In this work, we analyze several large-scale RRI datasets and identify low-complexity repeats (LCRs), including simple tandem repeats, as key drivers of RRIs. Our findings reveal that LCRs enable thermodynamically stable interactions with multiple partners, positioning them as key hubs in RNA-RNA interaction networks. These RRIs appear to be important for several aspects of RNA metabolism. Sequencing-based analysis of the lncRNA Lhx1os interactors validates the importance of LCRs in shaping contacts potentially involved in neuronal development. Recognizing the pivotal role of sequence determinants, we develop RIME, a deep learning model that predicts RRIs by leveraging embeddings from a nucleic acid language model. RIME outperforms traditional thermodynamics-based tools, successfully captures the role of LCRs and prioritizes high-confidence interactions, including those established by lncRNAs. RIME is freely available at https://tools.tartaglialab.com/rna_rna.
- assay: bulk RNA-seq
- research focus: gene regulatory network inference
- research focus: protein structure prediction
- research focus: drug response / drug discovery
- approach: deep learning
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