Lubitz Timo, Welkenhuysen Niek, Shashkova Sviatlana, Bendrioua Loubna, Hohmann Stefan, Klipp Edda, Krantz Marcus
Theoretical Biophysics, Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Chemistry and Molecular Biology, University of Gothenburg, Göteborg, Sweden.
NPJ Syst Biol Appl. 2015 Oct 22;1:15007. doi: 10.1038/npjsba.2015.7. eCollection 2015.
BACKGROUND/OBJECTIVES: The SNF1/AMPK protein kinase has a central role in energy homeostasis in eukaryotic cells. It is activated by energy depletion and stimulates processes leading to the production of ATP while it downregulates ATP-consuming processes. The yeast SNF1 complex is best known for its role in glucose derepression.
We performed a network reconstruction of the Snf1 pathway based on a comprehensive literature review. The network was formalised in the rxncon language, and we used the rxncon toolbox for model validation and gap filling.
We present a machine-readable network definition that summarises the mechanistic knowledge of the Snf1 pathway. Furthermore, we used the known input/output relationships in the network to identify and fill gaps in the information transfer through the pathway, to produce a functional network model. Finally, we convert the functional network model into a rule-based model as a proof-of-principle.
The workflow presented here enables large scale reconstruction, validation and gap filling of signal transduction networks. It is analogous to but distinct from that established for metabolic networks. We demonstrate the workflow capabilities, and the direct link between the reconstruction and dynamic modelling, with the Snf1 network. This network is a distillation of the knowledge from all previous publications on the Snf1/AMPK pathway. The network is a knowledge resource for modellers and experimentalists alike, and a template for similar efforts in higher eukaryotes. Finally, we envisage the workflow as an instrumental tool for reconstruction of large signalling networks across Eukaryota.
背景/目的:SNF1/AMPK蛋白激酶在真核细胞的能量稳态中起核心作用。它在能量耗竭时被激活,刺激导致ATP产生的过程,同时下调消耗ATP的过程。酵母SNF1复合体因其在葡萄糖去阻遏中的作用而最为人所知。
我们基于全面的文献综述对Snf1途径进行了网络重建。该网络用rxncon语言形式化,我们使用rxncon工具箱进行模型验证和缺口填充。
我们给出了一个机器可读的网络定义,总结了Snf1途径的机制知识。此外,我们利用网络中已知的输入/输出关系来识别和填补途径中信息传递的缺口,以生成一个功能网络模型。最后,作为原理验证,我们将功能网络模型转换为基于规则的模型。
本文介绍的工作流程能够对信号转导网络进行大规模重建、验证和缺口填充。它类似于但又不同于为代谢网络建立的工作流程。我们用Snf1网络展示了工作流程的能力以及重建与动态建模之间的直接联系。这个网络是以往所有关于Snf1/AMPK途径出版物知识的提炼。该网络是建模者和实验者的知识资源,也是高等真核生物类似研究的模板。最后,我们设想该工作流程是重建整个真核生物中大型信号网络的工具。