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arXiv cs.AI· Ziwei Yang, Takeyuki Tamura·· 4 小时前AI 评分33

HGPRGDel:面向生长耦合基因缺失设计的 GPR 感知学习与排序方法

HGPRGDel: GPR-Aware Learning and Ranking for Growth-Coupled Gene Deletion Design

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研究者提出 HGPRGDel 协议,通过显式表示基因-蛋白-反应(GPR)逻辑,学习并排序代谢工程中生长耦合生产的基因缺失优先级。在 e_coli_core、iMM904 和 iML1515 三个模型上,该协议在所评估学习配置中取得最高 macro-F1 和 AUC,其排序以少于基线方法的基因检验量平均回收 MetNetComp 参考缺失基因的 90%。

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Abstract:Designing microbial strains for growth-coupled production, in which cellular growth is linked to the synthesis of a target compound through genetic interventions, is a fundamental goal in metabolic engineering. Constraint-based methods can identify growth-coupled deletion strategies, but design for each target typically requires a separate search across a large number of possible gene-deletion combinations. This motivates a reusable approach that learns from previously evaluated strain designs to prioritize candidate interventions before downstream constraint-based evaluation. We present a reproducible protocol for growth-coupled gene deletion design that learns and ranks gene-deletion priorities for each target metabolite. Using computationally curated deletion strategies as learning resources, the protocol generates continuous deletion-priority rankings, constructs candidate strategies at adjustable search-space budgets, and evaluates these candidates through constraint-based metabolic analysis. Its learning component, HGPRGDel, explicitly represents gene-protein-reaction (GPR) logic, capturing how multiple genes can jointly support a reaction or alternative genes can maintain its activity, while integrating molecular and reaction-level information. Across e_coli_core, iMM904, and iML1515, the protocol achieves the highest macro-F1 and AUC among the evaluated learning configurations. HGPRGDel's rankings recovered an average of 90% of the reference deletion genes from MetNetComp by examining fewer genes than the evaluated baseline methods. By separating learned intervention prioritization from downstream constraint-based assessment, the protocol provides a reproducible framework for reusing strain-design knowledge while controlling the size of the candidate space and retaining mechanistic evaluation of growth-coupled production.
Subjects: Quantitative Methods (q-bio.QM); Artificial Intelligence (cs.AI)
Cite as: arXiv:2610.37478 [q-bio.QM]
  (or arXiv:2610.37478v1 [q-bio.QM] for this version)
  https://doi.org/10.48550/arXiv.2610.37478

arXiv-issued DOI via DataCite (pending registration)

Submission history

From: Ziwei Yang [view email]
[v1] Tue, 27 Oct 2026 16:07:02 UTC (1,140 KB)

来源:arXiv cs.AI · arxiv.org