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一种新的层次化方法,用于简化生物网络的 ODE 模型的多层次模型抽象,以及一个案例研究:哺乳动物细胞周期的 G1/S 检查点/DNA 损伤信号通路。

A new hierarchical approach to multi-level model abstraction for simplifying ODE models of biological networks and a case study: The G1/S Checkpoint/DNA damage signalling pathways of mammalian cell cycle.

机构信息

Complex Systems, Big Data and Informatics Initiative (CSBII), New Zealand.

Complex Systems, Big Data and Informatics Initiative (CSBII), New Zealand; Centre for Advanced Computational Solutions, Lincoln University, Christchurch, New Zealand.

出版信息

Biosystems. 2021 May;203:104374. doi: 10.1016/j.biosystems.2021.104374. Epub 2021 Feb 5.

Abstract

Model reduction is an important topic in studies of biological systems. By reducing the complexity of large models through multi-level models while keeping the essence (biological meaning) of the model, model reduction can help answer many important questions about these systems. In this paper, we present a new reduction method based on hierarchical representation and a lumping approach. We used G1/S checkpoint pathway represented in Ordinary Differential Equations (ODE) in Iwamoto et al. (2011) as a case study to present this reduction method. The approach consists of two parts; the first part represents the biological network as a hierarchy (multiple levels) based on protein binding relations, which allowed us to model the biological network at different levels of abstraction. The second part applies different levels (level 1, 2 and 3) of lumping the species together depending on the level of the hierarchy, resulting in a reduced and transformed model for each level. The model at each level is a representation of the whole system and can address questions pertinent to that level. We develop and simulate reduced models for levels-1, 2 and 3 of lumping for the G1/S checkpoint pathway and evaluate the biological plausibility of the proposed method by comparing the results with the original ODE model of Iwamoto et al. (2011). The results for continuous dynamics of the G1/S checkpoint pathway with or without DNA-damage for reduced models of level- 1, 2 and 3 of lumping are in very good agreement and consistent with the original model results and with biological findings. Therefore, the reduced models (level-1, 2 and 3) can be used to study cell cycle progression in G1 and the effects of DNA damage on it. It is suitable for reducing complex ODE biological network models while retaining accurate continuous dynamics of the system. The 3 levels of the reduced models respectively achieved 20%, 26% and 31% reduction of the base model. Moreover, the reduced model is more efficient to run (30%, 44% and 52% time reduction for the three levels) and generate solutions than the original ODE model. Simplification of complex mathematical models is possible and the proposed reduction method has the potential to make an impact across many fields of biomedical research.

摘要

模型约简是生物系统研究中的一个重要课题。通过多层次模型将大型模型的复杂性降低,同时保持模型的本质(生物学意义),模型约简可以帮助回答关于这些系统的许多重要问题。在本文中,我们提出了一种基于层次表示和聚类方法的新约简方法。我们使用 Iwamoto 等人(2011 年)提出的普通微分方程(ODE)中 G1/S 检查点途径作为案例研究来介绍这种约简方法。该方法由两部分组成;第一部分将生物网络表示为基于蛋白质结合关系的层次结构(多个层次),这使我们能够在不同的抽象层次上对生物网络进行建模。第二部分根据层次的不同,将物种聚集在一起的不同层次(第 1 层、第 2 层和第 3 层),从而为每个层次生成简化和转换后的模型。每个层次的模型都是整个系统的表示,可以解决与该层次相关的问题。我们为 G1/S 检查点途径的聚类第 1、2 和 3 层开发并模拟简化模型,并通过将结果与 Iwamoto 等人(2011 年)的原始 ODE 模型进行比较来评估所提出方法的生物学合理性。在没有 DNA 损伤的情况下,G1/S 检查点途径的连续动力学的简化模型的结果对于聚类的第 1、2 和 3 层的简化模型非常吻合且与原始模型的结果以及生物学发现一致。因此,简化模型(第 1、2 和 3 层)可用于研究 G1 中的细胞周期进展以及 DNA 损伤对其的影响。它适用于在保留系统准确连续动力学的同时简化复杂的 ODE 生物网络模型。简化模型分别实现了基础模型的 20%、26%和 31%的减少。此外,简化模型比原始 ODE 模型运行更高效(三个层次的时间减少 30%、44%和 52%)并且生成解决方案。复杂数学模型的简化是可能的,所提出的约简方法有可能对生物医学研究的许多领域产生影响。

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