This work describes a conditional generative framework for 50-nt modified-RNA 5'UTR design that optionally conditions on ribosome load, GC content, minimum free energy, and target secondary structure and uses a Transformer-based generator followed by sequence ranking and local refinement.
Abstract
The 5'untranslated region is a major determinant of translation initiation, and its effect becomes especially important in modified mRNA sequences, where start-codon context, cap-proximal secondary structure, upstream AUGs and upstream open reading frames, and nucleotide chemistry can alter ribosome scanning and initiation recruitment, scanning, and decoding in sequence-dependent ways. Recent computational studies have moved the field from prediction toward design, including massively trained predictive models such as Smart5UTR for m1$\Psi$-modified mRNA, broader 5'UTR generation and optimization frameworks such as UTRGAN and UTailoR, and structure-guided RNA design systems such as RhoDesign. Here, we describe a conditional generative framework for 50-nt modified-RNA 5'UTR design that optionally conditions on ribosome load, GC content, minimum free energy, and target secondary structure. The implementation uses a Transformer-based generator followed by sequence ranking and local refinement with a Smart5UTR-derived ribosome-load oracle and ViennaRNA-based folding metrics, including support for modified-base folding parameters. Across multiple simulation scenarios and experimental settings, different combinations of RL, GC, MFE, and structural constraints produced distinct performance tradeoffs, enabling ablation-based identification of the best-performing formulation.
RIFT-VAE is best interpreted as a hybrid generative-search framework: pretraining supplies a structure- and family-informed proposal distribution, whereas latent optimization concentrates evaluations in high-scoring regions.
The 5′ untranslated region (5′ UTR) shapes translation initiation, so its design is central to mRNA therapeutics and to improving protein-production cell lines. Deep-learning models that predict translation efficiency, measured as mean ribosome load (MRL), from the 5′ UTR sequence have been combined with genetic algori...
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