Evidence map›Paper›PMID 41775687›Full record

ArticleNature communications2026

Cross-species gene redesign leveraging ortholog information and generative modeling.

Manato Akiyama, Motohiko Tashiro, Ying Huang, Mika Uehara, Taiki Kanzaki, Mitsuhiro Itaya, Masakazu Kataoka, Kenji Miyamoto, Yasubumi Sakakibara

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Manato Akiyama *Department of Data Science, Kitasato University School of Frontier Engineering, Sagamihara, Kanagawa, Japan.
Motohiko Tashiro *Department of Biosciences and Informatics, Keio University, Yokohama, Kanagawa, Japan.
Ying Huang *Department of Biosciences and Informatics, Keio University, Yokohama, Kanagawa, Japan.
Mika UeharaDepartment of Data Science, Kitasato University School of Frontier Engineering, Sagamihara, Kanagawa, Japan.ORCID 0000-0002-7407-1923
Taiki KanzakiDepartment of Biomedical Engineering, Shinshu University, Nagano-shi, Nagano, Japan.
Mitsuhiro ItayaDepartment of Biomedical Engineering, Shinshu University, Nagano-shi, Nagano, Japan.
Masakazu KataokaDepartment of Biomedical Engineering, Shinshu University, Nagano-shi, Nagano, Japan.
Kenji MiyamotoDepartment of Biosciences and Informatics, Keio University, Yokohama, Kanagawa, Japan.
Yasubumi SakakibaraDepartment of Data Science, Kitasato University School of Frontier Engineering, Sagamihara, Kanagawa, Japan. sakakibara.yasubumi@kitasato-u.ac.jp.ORCID 0000-0002-6932-3452

Funding

MEXT | JST | Core Research for Evolutional Science and Technology (CREST) JPMJCR20S3
6 · The paper itself

Abstract

Conventional approaches to heterologous gene expression rely on codon optimization, which is limited to swapping synonymous codons and fails to capture deeper adaptive changes. In contrast, naturally evolved orthologous genes include non-synonymous mutations, insertions, and deletions that confer functional adaptation to different host contexts. Here we present OrthologTransformer, a Transformer-based deep learning model that converts orthologous genes between species by learning from large-scale orthologous gene datasets. The model recapitulates evolutionary differences-from synonymous codon swaps to amino acid-changing mutations and indels-to predict coding sequences optimized for target species while preserving protein function. In extensive tests across diverse bacterial species pairs, the model's context-aware gene designs more closely resembled native host orthologs, preserved protein functionality, and achieved superior expression yields compared to codon-optimized sequences. As proof of concept, an OrthologTransformer-redesigned PETase expressed in Bacillus subtilis showed robust activity, producing approximately 10-fold more reaction product than the codon-optimized enzyme, and achieving higher expression levels, thereby demonstrating improved enzyme performance via AI-guided gene design.

Indexed as

Models, GeneticBacillus subtilisBacterial ProteinsCodonDeep LearningEvolution, MolecularBacterial ProteinsCodon

Identifiers

PMID41775687
PMCPMC12957437

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.