GEMsembler:共识模型组装和跨工具基因组尺度代谢模型的结构比较提高功能性能。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-08 DOI:10.1128/msystems.00574-25
Elena K Matveishina, Bartosz J Bartmanski, Sara Benito-Vaquerizo, Maria Zimmermann-Kogadeeva
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引用次数: 0

摘要

基因组尺度代谢模型(GEMs)在系统生物学中广泛用于研究代谢和预测扰动响应。自动GEM重建工具为同一生物体生成具有不同属性和预测能力的GEM。由于不同的模型可以擅长不同的任务,因此将它们结合起来可以增加代谢网络的确定性,提高模型的性能。在这里,我们介绍GEMsembler,这是一个Python包,用于比较跨工具的GEMs,跟踪模型特征的起源,并构建包含输入模型的任意子集的共识模型。GEMsembler提供全面的分析功能,包括生物合成途径的识别和可视化、生长评估和基于协议的管理工作流程。由四种植物乳酸杆菌和大肠杆菌自动重建的gemsembler管理的共识模型在营养缺陷和基因必要性预测方面优于金标准模型。从共识模型中优化基因-蛋白-反应(GPR)组合可以改善基因本质预测,即使在人工策划的金标准模型中也是如此。GEMsembler通过强调相关的代谢途径和GPR替代方案来解释模型性能,为实验提供信息以解决模型的不确定性。因此,GEMsembler有助于为系统生物学应用建立更准确和生物学知情的代谢模型。基因组尺度的代谢模型(GEMs)捕获了我们在基因组中编码的细胞代谢知识,使我们能够描述和预测细胞在不同条件下的功能。虽然一些自动化工具可以直接从基因组数据生成这些模型,但所得到的模型通常包含空白和不确定性,突出了我们的代谢知识不完整的领域。在这里,我们介绍了一个名为GEMsembler的新工具,它集成了由不同方法构建的GEMs,评估模型不确定性,并构建共识模型,利用每种方法的独特功能。这些共识模型更准确地反映了实验观察到的代谢特征,如营养需求和条件特异性基因的必要性。GEMsembler有助于对模型结构和功能进行全面分析,帮助确定知识差距并优先考虑实验以解决这些问题。通过综合来自不同来源的信息,GEMsembler加速了更可靠和具有生物学意义的模型的开发,推进了代谢工程、病原体生物学和微生物群落研究的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GEMsembler: consensus model assembly and structural comparison of genome-scale metabolic models across tools improve functional performance.

Genome-scale metabolic models (GEMs) are widely used in systems biology to investigate metabolism and predict perturbation responses. Automatic GEM reconstruction tools generate GEMs with different properties and predictive capacities for the same organism. Since different models can excel at different tasks, combining them can increase metabolic network certainty and enhance model performance. Here, we introduce GEMsembler, a Python package designed to compare cross-tool GEMs, track the origin of model features, and build consensus models containing any subset of the input models. GEMsembler provides comprehensive analysis functionality, including identification and visualization of biosynthesis pathways, growth assessment, and an agreement-based curation workflow. GEMsembler-curated consensus models built from four Lactiplantibacillus plantarum and Escherichia coli automatically reconstructed models outperform the gold-standard models in auxotrophy and gene essentiality predictions. Optimizing gene-protein-reaction (GPR) combinations from consensus models improves gene essentiality predictions, even in the manually curated gold-standard models. GEMsembler explains model performance by highlighting relevant metabolic pathways and GPR alternatives, informing experiments to resolve model uncertainty. Thus, GEMsembler facilitates building more accurate and biologically informed metabolic models for systems biology applications.IMPORTANCEGenome-scale metabolic models (GEMs) capture our knowledge of cellular metabolism as encoded in the genome, enabling us to describe and predict how cells function under different conditions. While several automated tools can generate these models directly from genome data, the resulting models often contain gaps and uncertainties, highlighting areas where our metabolic knowledge is incomplete. Here, we introduce a new tool called GEMsembler, which integrates GEMs constructed by different methods, evaluate model uncertainty, and build consensus models, harnessing the unique features of each approach. These consensus models more accurately reflect experimentally observed metabolic traits, such as nutrient requirements and condition-specific gene essentiality. GEMsembler facilitates comprehensive analysis of model structure and function, helping to pinpoint knowledge gaps and prioritize experiments to address them. By synthesizing information from diverse sources, GEMsembler accelerates the development of more reliable and biologically meaningful models, advancing research in metabolic engineering, pathogen biology, and microbial community studies.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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