Generative modeling for RNA splicing prediction and design
Alternative splicing (AS) of pre-mRNA plays a crucial role in tissue-specific gene regulation, with disease implications due to splicing defects. Predicting and manipulating AS can therefore uncover new regulatory mechanisms and aid in therapeutic design. We introduce TrASPr+BOS, a generative AI model with Bayesian Optimization for predicting and designing RNA for tissue-specific splicing outcomes. Transformer for Alternative Splicing Prediction (TrASPr) is a multi-transformer model that can handle different types of AS events and generalize to unseen cellular conditions. It then serves as an oracle, generating labeled data to train a Bayesian Optimization for Splicing (BOS) algorithm to design RNA for condition-specific splicing outcomes. We show TrASPr+BOS outperforms existing methods, enhancing tissue-specific AUPRC by up to 1.8-fold and capturing tissue-specific regulatory elements. We validate hundreds of predicted novel tissue-specific splicing variations and confirm new regulatory elements using dCas13. We envision TrASPr+BOS as a light yet accurate method researchers can probe or adopt for specific tasks.
Authors
- Natalie Maus (ORCID: https://orcid.org/0000-0002-6616-8506)
- Yoseph Barash (ORCID: https://orcid.org/0000-0003-3005-5048)
- San Jewell (ORCID: https://orcid.org/0000-0002-6494-8015)
- Anupama Jha (ORCID: https://orcid.org/0000-0003-3029-2086)
- Jake R. Gardner
- Di Wu (ORCID: https://orcid.org/0000-0002-3440-1860)
- Benjamin D Wales-McGrath (ORCID: https://orcid.org/0009-0006-4184-7875)
- Anna Tangiyan
- Peter Choi
- Kevin Yang
Institutions
- Children's Hospital of Philadelphia (US)
- University of Washington (US)
- University of Pennsylvania (US)
Publication Details
- Journal
- eLife
- Published
- 2026-05-29
- DOI
- https://doi.org/10.7554/elife.106043.3
- Primary Topic
- RNA Research and Splicing
- Type
- article
- Field-Weighted Citation Impact
- 0.00