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首页> 外文期刊>PLoS Computational Biology >redGEM: Systematic reduction and analysis of genome-scale metabolic reconstructions for development of consistent core metabolic models
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redGEM: Systematic reduction and analysis of genome-scale metabolic reconstructions for development of consistent core metabolic models

机译:redGEM:系统化减少和分析基因组规模的代谢重建,以开发一致的核心代谢模型

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Genome-scale metabolic reconstructions have proven to be valuable resources in enhancing our understanding of metabolic networks as they encapsulate all known metabolic capabilities of the organisms from genes to proteins to their functions. However the complexity of these large metabolic networks often hinders their utility in various practical applications. Although reduced models are commonly used for modeling and in integrating experimental data, they are often inconsistent across different studies and laboratories due to different criteria and detail, which can compromise transferability of the findings and also integration of experimental data from different groups. In this study, we have developed a systematic semi-automatic approach to reduce genome-scale models into core models in a consistent and logical manner focusing on the central metabolism or subsystems of interest. The method minimizes the loss of information using an approach that combines graph-based search and optimization methods. The resulting core models are shown to be able to capture key properties of the genome-scale models and preserve consistency in terms of biomass and by-product yields, flux and concentration variability and gene essentiality. The development of these “consistently-reduced” models will help to clarify and facilitate integration of different experimental data to draw new understanding that can be directly extendable to genome-scale models.
机译:基因组规模的代谢重建已被证明是增进我们对代谢网络了解的宝贵资源,因为它们封装了生物体从基因到蛋白质到其功能的所有已知代谢能力。然而,这些大型代谢网络的复杂性常常阻碍了它们在各种实际应用中的实用性。尽管简化模型通常用于建模和集成实验数据,但由于不同的标准和细节,它们在不同的研究和实验室之间常常是不一致的,这可能会损害研究结果的可移植性以及来自不同组的实验数据的集成。在这项研究中,我们开发了一种系统的半自动方法,以一致且合乎逻辑的方式将基因组规模模型简化为核心模型,重点关注中心代谢或目标子系统。该方法使用结合了基于图的搜索和优化方法的方法来最大程度地减少信息丢失。结果表明,所得的核心模型能够捕获基因组规模模型的关键特性,并在生物量和副产物产量,通量和浓度变异性以及基因必要性方面保持一致性。这些“一致减少的”模型的开发将有助于阐明和促进不同实验数据的整合,以得出可以直接扩展到基因组规模模型的新理解。

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