生物网络的模块化控制

ArXiv Pub Date : 2024-11-04
David Murrugarra, Alan Veliz-Cuba, Elena Dimitrova, Claus Kadelka, Matthew Wheeler, Reinhard Laubenbacher
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引用次数: 0

摘要

控制的概念是理解和应用生物网络模型的核心。它们的一些关键结构特征与通过基因调控、信号传导或代谢机制实现的控制功能有关,而计算模型需要对这些功能进行编码。模型的应用通常侧重于基于模型的控制,如生物医学或代谢工程。本文介绍了一种基于模型的控制方法,它利用了生物网络的两个共同特征,即模块化结构和调控机制的渠化特征。本文的重点是以布尔网络模型为代表的细胞内调控网络。本文的一个主要成果是,可以通过一次只关注一个模块来确定控制策略。本文还提出了一种基于调控规则渠化特征的标准,以识别对网络控制无贡献的模块,并将其排除在外。即使对于中等规模的网络,寻找全局控制输入在计算上也非常具有挑战性。本文介绍的模块化方法是解决这一问题的高效方法。本文将这种方法应用于已发表的血癌大颗粒淋巴细胞(T-LGL)白血病布尔网络模型,以确定能实现预期控制目标的最小控制集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modular control of Boolean network models.

The concept of control is crucial for effectively understanding and applying biological network models. Key structural features relate to control functions through gene regulation, signaling, or metabolic mechanisms, and computational models need to encode these. Applications often focus on model-based control, such as in biomedicine or metabolic engineering. In a recent paper, the authors developed a theoretical framework of modularity in Boolean networks, which lead to a canonical semidirect product decomposition of these systems. In this paper, we present an approach to model-based control that exploits this modular structure, as well as the canalizing features of the regulatory mechanisms. We show how to identify control strategies from the individual modules, and we present a criterion based on canalizing features of the regulatory rules to identify modules that do not contribute to network control and can be excluded. For even moderately sized networks, finding global control inputs is computationally challenging. Our modular approach leads to an efficient approach to solving this problem. We apply it to a published Boolean network model of blood cancer large granular lymphocyte (T-LGL) leukemia to identify a minimal control set that achieves a desired control objective.

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