Evidence map›Paper›PMID 41693567›Full record

ArticleNucleic acids research2026

Design prokaryotic cis-regulatory elements using language model.

Yan Xia, Jinyuan Sun, Xiaowen Du, Zeyu Liang, Xin Wu, Wenyu Shi, Bin Shao, Shuyuan Guo, Yi-Xin Huo

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yan XiaDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.
Jinyuan SunCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.ORCID 0000-0003-3456-0332
Xiaowen DuDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.
Zeyu LiangDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.
Xin WuDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.
Wenyu ShiState Key Laboratory of Animal Biotech Breeding, College of Biological Sciences, China Agricultural University, Beijing 100083, China.
Bin ShaoAdvanced Research Institute of Multidisciplinary Sciences, Beijing Institute of Technology, Beijing 100081, China.
Shuyuan GuoDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.ORCID 0000-0001-7801-2528
Yi-Xin HuoDepartment of Gastroenterology, Aerospace Center Hospital, College of Life Science, Beijing Institute of Technology, Beijing 100081, China.ORCID 0000-0003-4644-999X

Funding

National Key R&D Program of China 2024YFA0917501National Natural Science Foundation of China 32370095National Natural Science Foundation of China 32371489
6 · The paper itself

Abstract

Deep learning has successfully been applied to design cis-regulatory elements (CREs) for a few species, but a broadly applicable platform for generating functional promoters for thousands of prokaryotes remains lacking. In this study, we introduce a language model for prokaryotic CREs, referred to as PromoGen2, to design CREs without prior experimental data. PromoGen2 was pretrained on CREs derived from 17 000 prokaryotic genomes. It achieved the highest zero-shot prediction correlation of promoter strength across species, improving the average Spearman correlation from 0.27 to 0.50 compared to the best baseline, while reducing the number of parameters by 103. Artificial CREs designed with PromoGen2 demonstrated a 100% success rate in Escherichia coli, Bacillus subtilis, Bacillus licheniformis, and Agrobacterium tumefaciens. Based on PromoGen2, we developed the Promoter-Factory framework to design promoters from unannotated genomes. Experimental validation showed that most of the promoters designed for Jejubacter sp. L23, a newly isolated halophilic bacterium with no available CREs, were active and capable of driving lycopene overproduction. Additionally, we introduced PromoGen2-proka, a taxonomy-aware model for CRE design based on prokaryotic genera. Experimental validation confirmed its reliable success rate. The combined use of PromoGen2-proka and Promoter-Factory offers a broadly applicable tool for designing CREs for prokaryotes, fulfilling the needs of synthetic biology and microbiology research.

Indexed as

Promoter Regions, GeneticBacillus subtilisDeep LearningEscherichia coliGenome, BacterialLarge Language ModelsLycopeneLycopene

Identifiers

PMID41693567
PMCPMC12907563

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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.