A knowledge representation meta-model for rule-based modelling of signalling networks

Adrien Basso-Blandin, W. Fontana, Russell Harmer
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引用次数: 13

Abstract

The study of cellular signalling pathways and their deregulation in disease states, such as cancer, is a large and extremely complex task. Indeed, these systems involve many parts and processes but are studied piecewise and their literatures and data are consequently fragmented, distributed and sometimes--at least apparently--inconsistent. This makes it extremely difficult to build significant explanatory models with the result that effects in these systems that are brought about by many interacting factors are poorly understood. The rule-based approach to modelling has shown some promise for the representation of the highly combinatorial systems typically found in signalling where many of the proteins are composed of multiple binding domains, capable of simultaneous interactions, and/or peptide motifs controlled by post-translational modifications. However, the rule-based approach requires highly detailed information about the precise conditions for each and every interaction which is rarely available from any one single source. Rather, these conditions must be painstakingly inferred and curated, by hand, from information contained in many papers--each of which contains only part of the story. In this paper, we introduce a graph-based meta-model, attuned to the representation of cellular signalling networks, which aims to ease this massive cognitive burden on the rule-based curation process. This meta-model is a generalization of that used by Kappa and BNGL which allows for the flexible representation of knowledge at various levels of granularity. In particular, it allows us to deal with information which has either too little, or too much, detail with respect to the strict rule-based meta-model. Our approach provides a basis for the gradual aggregation of fragmented biological knowledge extracted from the literature into an instance of the meta-model from which we can define an automated translation into executable Kappa programs.
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基于规则的信令网络建模的知识表示元模型
研究细胞信号通路及其在疾病状态(如癌症)中的解除管制是一项庞大而极其复杂的任务。事实上,这些系统涉及许多部分和过程,但被分段地研究,因此它们的文献和数据是碎片化的、分散的,有时(至少在表面上)是不一致的。这使得建立重要的解释性模型变得极其困难,结果是这些系统中由许多相互作用的因素所带来的影响很难理解。基于规则的建模方法已经显示出一些希望,用于表示通常在信号传导中发现的高度组合系统,其中许多蛋白质由多个结合域组成,能够同时相互作用,和/或由翻译后修饰控制的肽基序。然而,基于规则的方法需要关于每个交互的精确条件的非常详细的信息,这些信息很少从任何单一来源获得。相反,这些条件必须从许多论文中的信息中精心推断和手工策划——每一篇论文都只包含了故事的一部分。在本文中,我们引入了一个基于图的元模型,该模型与细胞信号网络的表示相适应,旨在减轻基于规则的管理过程中的这种巨大的认知负担。这个元模型是Kappa和BNGL使用的元模型的泛化,它允许在不同粒度级别上灵活地表示知识。特别是,它允许我们处理相对于严格的基于规则的元模型来说细节太少或太多的信息。我们的方法为从文献中提取的碎片化生物学知识逐渐聚集到元模型实例中提供了基础,从中我们可以定义自动翻译为可执行的Kappa程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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