bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.11.07.687268

Designing Convergent Overlapping Genes with Transformer Encoder Models and Lightweight Structural Proxies

Abstract

Overlapping genes allow multiple proteins to be encoded from a single DNA sequence, including convergent (antisense; tail-to-tail) orientations across three reading frames (phases 0, 1, and 2), with phase 1 most frequently observed in nature. Designing such overlaps is challenging due to codon degeneracy, phase-specific biases, and the need to preserve structural integrity for both proteins. Here, a purpose-built transformer encoder is introduced, trained on a balanced synthetic dataset of convergent overlaps spanning diverse prokaryotic genomes and GC contents. Controlled amino acid substitutions were incorporated during training to enhance model generalization, particularly for phase 1 overlaps. At inference, Monte Carlo dropout enabled uncertainty-aware sampling of synonymous codon solutions, which were iteratively refined using a windowed, multi-objective optimization framework. Candidate overlaps were scored using composite weighting across secondary structure preservation, substitution similarity, alignment identity, and ESM-2 contact map similarity, with the structural similarity index measure (SSIM) applied as a rapid proxy for structural fidelity. This approach generated convergent overlaps across all phases, with phase 1 showing the highest success rates. Optimization trajectories revealed distinct dynamics, with secondary structure preservation steadily increasing despite its lower weight. External validation using SwissProt proteins stratified by AlphaFold2 (AF2) predicted local distance difference test (pLDDT) confidence supported generalization to proteins with differing rigidity, yielding high secondary structure preservation in silico. These results demonstrate that transformer models trained directly at the nucleotide level, when coupled with uncertainty-aware inference and lightweight structural proxies, can support the computational design of synthetic overlapping genes without requiring full structural prediction. This framework offers a scalable path for phase-specific, codon-aware overlap design under realistic constraints.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Morgan, J. K.. 2025-11-10. Designing Convergent Overlapping Genes with Transformer Encoder Models and Lightweight Structural Proxies. https://doi.org/10.1101/2025.11.07.687268

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Gene expression noise is reduced in communicating synthetic cell populations

A major goal in bottom-up synthetic biology is the construction of multicellular synthetic systems capable of coordinated and robust collective behaviours. However, robustness is often limited by noise and variability arising from increased molecular complexity. Whilst communication has been implemented in synthetic multi-cellular systems, the ability for communication to suppress cell free gene expression variability in populations of synthetic cells remain unexplored. To address this, we encapsulated the Lux and Las quorum sensing gene circuits in lipid vesicles under cell-free conditions to test the effect of communication on reducing cell-free gene expression variability across the population. Our results show that communication, limiting expression resources, and membrane surface effects can reduce gene expression variability. Resource limited Gillespie simulations for transcription and translation show that communication-mediated coupling reduces population-level expression noise under constrained and excess resource conditions. Together, our work provides simple strategies to reduce gene expression variability and thereby improve robustness in synthetic multicellular systems, an important criteria for the future applications of synthetic cells.

synthetic biology↗

Boolean Logic-responsive FRET Biosensors via Genetically Encoded Autonomous Compilation

Forster resonance energy transfer (FRET) is commonly used to monitor protein-protein interactions in situ. The high spatiotemporal resolution and facile implementation inside complex molecular environments have spearheaded FRET's widespread adoption in biosensing. Despite these advantages, current FRET biosensors are largely restricted to the detection of the presence/absence of individual inputs and are thus unable to sense several multiplexable inputs simultaneously within complex milieu of biological environments. In this work, we introduce a generalizable strategy to construct genetically encoded protein-based FRET biosensors capable of recognizing multiple inputs following Boolean logic-type (YES/OR/AND) operations. These topologically specified FRET sensors powerfully expand the input capacity in sensing protein-protein interactions while providing a user-programmable platform for monitoring heterogeneous biological activities both in vitro and in living cells.

synthetic biology↗

AI-Guided Multi-Objective Engineering of Glucoamylase Enables Acidification-Free Starch Saccharification

Glucoamylase is essential for industrial starch saccharification, but the limited thermostability and near-neutral pH tolerance of fungal glucoamylases necessitate cooling and acidification of liquefied starch. Here, we developed an artificial intelligence-guided strategy to simultaneously improve the thermostability, pH tolerance, and catalytic activity of glucoamylase from Penicillium oxalicum (PoGA). Two property-specific machine-learning models, CASPE-T and CASPE-A, identified substitutions associated with thermostability and pH tolerance, respectively. Experimental screening identified beneficial substitutions in 11 of 21 CASPE-T and 12 of 22 CASPE-A candidates. Folding-energy-guided recombination integrated the two traits while maintaining structural compatibility. The optimal variant, PoGA T513E/Q305N, exhibited 2.21-fold higher specific activity than the wild type, with half-life extended from 22.3 to 57.9 min at 60 degrees C and from 16.6 to 64.7 min at pH 8.0. Molecular dynamics simulations attributed these improvements to reinforcement of high-occupancy hydrogen-bonding networks, suppression of conformational fluctuations in the linker and carbohydrate-binding module, enhanced long-range dynamic coordination, and preservation of a compact catalytic architecture. At 60 degrees C and pH 6.5 without acidification, PoGA T513E/Q305N produced 219.9 g/L glucose and achieved 89.1% starch conversion, 31.4% higher than the wild type. This work provides an efficient framework for multi-objective enzyme engineering and sustainable starch biorefining.

synthetic biology↗