Advancing codon language modeling with synonymous codon constrained masking

Codon language models offer a promising framework for modeling protein-coding DNA sequences, yet current approaches often conflate codon usage with amino acid semantics, limiting their ability to capture DNA-level biology. We introduce SynCodonLM, a codon language model that enforces a biologically grounded constraint: masked codons are only predicted from synonymous options, guided by the known protein sequence. This design disentangles codon-level from protein-level semantics, enabling the model to learn nucleotide-specific patterns. The constraint is implemented by masking non-synonymous codons from the prediction space prior to softmax. Unlike existing models, which cluster codons by amino acid identity, SynCodonLM clusters by nucleotide properties, revealing structure aligned with DNA-level biology. Furthermore, SynCodonLM outperforms existing models on six of seven benchmarks sensitive to DNA-level features, including messenger RNA and protein expression. Our approach advances domain-specific representation learning and opens avenues for sequence design in synthetic biology, as well as deeper insights into diverse bioprocesses.

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Publication Details

Journal
Nucleic Acids Research
Published
2026-02-14
DOI
https://doi.org/10.1093/nar/gkag166
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

Advancing codon language modeling with synonymous codon constrained masking

Andrew E. Nixon, Noah Pefaur, Laura J. Kingsley, James Heuschkel et al.
Nucleic Acids Research
RNA and protein synthesis mechanisms
article

Advancing codon language modeling with synonymous codon constrained masking

Andrew E. Nixon, Noah Pefaur, Laura J. Kingsley, James Heuschkel, Steven Cramer
article en

Abstract

Codon language models offer a promising framework for modeling protein-coding DNA sequences, yet current approaches often conflate codon usage with amino acid semantics, limiting their ability to capture DNA-level biology. We introduce SynCodonLM, a codon language model that enforces a biologically grounded constraint: masked codons are only predicted from synonymous options, guided by the known protein sequence. This design disentangles codon-level from protein-level semantics, enabling the model to learn nucleotide-specific patterns. The constraint is implemented by masking non-synonymous codons from the prediction space prior to softmax. Unlike existing models, which cluster codons by amino acid identity, SynCodonLM clusters by nucleotide properties, revealing structure aligned with DNA-level biology. Furthermore, SynCodonLM outperforms existing models on six of seven benchmarks sensitive to DNA-level features, including messenger RNA and protein expression. Our approach advances domain-specific representation learning and opens avenues for sequence design in synthetic biology, as well as deeper insights into diverse bioprocesses.

Nucleic Acids ResearchVol. 54(5)
Rensselaer Polytechnic Institute (US), Boehringer Ingelheim (Spain) (ES)
Quality Education
Openalex Percentile: Top 42%
RNA and protein synthesis mechanisms
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