{"title":"整合DNA序列和转录起始信号的可解释深度学习框架用于基因表达预测。","authors":"Jianbo Qiao, Wenjia Gao, Ding Wang, Junru Jin, Siqi Chen, Zhongmin Yan, Leyi Wei","doi":"10.1021/acssynbio.6c00275","DOIUrl":null,"url":null,"abstract":"<p>Gene expression is a fundamental process in cellular\r\nfunction and\r\norganismal phenotype formation, governed by intricate and finely tuned\r\nregulatory mechanisms. Deciphering the regulatory code of gene expression\r\nand elucidating the transcriptional effects of the genome remain critical\r\nchallenges in human genetics. While numerous deep learning approaches\r\nhave been developed to predict gene expression levels, most prioritize\r\nDNA sequence information, often overlooking the impact of transcription\r\ninitiation signals and lacking interpretability regarding both model\r\nbehavior and feature contributions. In this study, we present an interpretable\r\ndeep learning framework based on convolutional neural networks with\r\na Gated Recurrent Unit. This method efficiently predicts gene expression\r\nlevels by integrating DNA sequence data, mRNA half-life features,\r\nand transcription initiation signals. We further validate the model\r\non GM12878, HepG2, and K562 data sets, demonstrating its robustness\r\nacross different human cell lines. Moreover, interpretability analysis\r\ndemonstrates that the model provides valuable insights into gene expression\r\nmechanisms, underscoring its practical utility as a robust tool for\r\nunderstanding and predicting gene expression levels.</p>","PeriodicalId":26,"journal":{"name":"ACS Synthetic Biology","volume":"15 8","pages":"3403–3412"},"PeriodicalIF":4.5000,"publicationDate":"2026-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An Explainable Deep Learning Framework Integrating DNA Sequence and Transcription Initiation Signals for Gene Expression Prediction\",\"authors\":\"Jianbo Qiao, Wenjia Gao, Ding Wang, Junru Jin, Siqi Chen, Zhongmin Yan, Leyi Wei\",\"doi\":\"10.1021/acssynbio.6c00275\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Gene expression is a fundamental process in cellular\\r\\nfunction and\\r\\norganismal phenotype formation, governed by intricate and finely tuned\\r\\nregulatory mechanisms. Deciphering the regulatory code of gene expression\\r\\nand elucidating the transcriptional effects of the genome remain critical\\r\\nchallenges in human genetics. While numerous deep learning approaches\\r\\nhave been developed to predict gene expression levels, most prioritize\\r\\nDNA sequence information, often overlooking the impact of transcription\\r\\ninitiation signals and lacking interpretability regarding both model\\r\\nbehavior and feature contributions. In this study, we present an interpretable\\r\\ndeep learning framework based on convolutional neural networks with\\r\\na Gated Recurrent Unit. This method efficiently predicts gene expression\\r\\nlevels by integrating DNA sequence data, mRNA half-life features,\\r\\nand transcription initiation signals. We further validate the model\\r\\non GM12878, HepG2, and K562 data sets, demonstrating its robustness\\r\\nacross different human cell lines. Moreover, interpretability analysis\\r\\ndemonstrates that the model provides valuable insights into gene expression\\r\\nmechanisms, underscoring its practical utility as a robust tool for\\r\\nunderstanding and predicting gene expression levels.</p>\",\"PeriodicalId\":26,\"journal\":{\"name\":\"ACS Synthetic Biology\",\"volume\":\"15 8\",\"pages\":\"3403–3412\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2026-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Synthetic Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acssynbio.6c00275\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/7/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssynbio.6c00275","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
An Explainable Deep Learning Framework Integrating DNA Sequence and Transcription Initiation Signals for Gene Expression Prediction
Gene expression is a fundamental process in cellular
function and
organismal phenotype formation, governed by intricate and finely tuned
regulatory mechanisms. Deciphering the regulatory code of gene expression
and elucidating the transcriptional effects of the genome remain critical
challenges in human genetics. While numerous deep learning approaches
have been developed to predict gene expression levels, most prioritize
DNA sequence information, often overlooking the impact of transcription
initiation signals and lacking interpretability regarding both model
behavior and feature contributions. In this study, we present an interpretable
deep learning framework based on convolutional neural networks with
a Gated Recurrent Unit. This method efficiently predicts gene expression
levels by integrating DNA sequence data, mRNA half-life features,
and transcription initiation signals. We further validate the model
on GM12878, HepG2, and K562 data sets, demonstrating its robustness
across different human cell lines. Moreover, interpretability analysis
demonstrates that the model provides valuable insights into gene expression
mechanisms, underscoring its practical utility as a robust tool for
understanding and predicting gene expression levels.
期刊介绍:
The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism.
Topics may include, but are not limited to:
Design and optimization of genetic systems
Genetic circuit design and their principles for their organization into programs
Computational methods to aid the design of genetic systems
Experimental methods to quantify genetic parts, circuits, and metabolic fluxes
Genetic parts libraries: their creation, analysis, and ontological representation
Protein engineering including computational design
Metabolic engineering and cellular manufacturing, including biomass conversion
Natural product access, engineering, and production
Creative and innovative applications of cellular programming
Medical applications, tissue engineering, and the programming of therapeutic cells
Minimal cell design and construction
Genomics and genome replacement strategies
Viral engineering
Automated and robotic assembly platforms for synthetic biology
DNA synthesis methodologies
Metagenomics and synthetic metagenomic analysis
Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction
Gene optimization
Methods for genome-scale measurements of transcription and metabolomics
Systems biology and methods to integrate multiple data sources
in vitro and cell-free synthetic biology and molecular programming
Nucleic acid engineering.