University of Ulster, School of Biomedical Sciences, Cromore Road, Coleraine BT52 1SA, Co, Londonderry, UK.
BMC Bioinformatics. 2010 Sep 14;11:459. doi: 10.1186/1471-2105-11-459.
A gene-regulatory network (GRN) refers to DNA segments that interact through their RNA and protein products and thereby govern the rates at which genes are transcribed. Creating accurate dynamic models of GRNs is gaining importance in biomedical research and development. To improve our understanding of continuous deterministic modeling methods employed to construct dynamic GRN models, we have carried out a comprehensive comparative study of three commonly used systems of ordinary differential equations: The S-system (SS), artificial neural networks (ANNs), and the general rate law of transcription (GRLOT) method. These were thoroughly evaluated in terms of their ability to replicate the reference models' regulatory structure and dynamic gene expression behavior under varying conditions.
While the ANN and GRLOT methods appeared to produce robust models even when the model parameters deviated considerably from those of the reference models, SS-based models exhibited a notable loss of performance even when the parameters of the reverse-engineered models corresponded closely to those of the reference models: this is due to the high number of power terms in the SS-method, and the manner in which they are combined. In cross-method reverse-engineering experiments the different characteristics, biases and idiosynchracies of the methods were revealed. Based on limited training data, with only one experimental condition, all methods produced dynamic models that were able to reproduce the training data accurately. However, an accurate reproduction of regulatory network features was only possible with training data originating from multiple experiments under varying conditions.
The studied GRN modeling methods produced dynamic GRN models exhibiting marked differences in their ability to replicate the reference models' structure and behavior. Our results suggest that care should be taking when a method is chosen for a particular application. In particular, reliance on only a single method might unduly bias the results.
基因调控网络(GRN)是指通过其 RNA 和蛋白质产物相互作用的 DNA 片段,从而控制基因转录的速率。创建 GRN 的准确动态模型在生物医学研究和开发中变得越来越重要。为了提高我们对用于构建动态 GRN 模型的连续确定性建模方法的理解,我们对三种常用的常微分方程系统进行了全面的比较研究:S 系统(SS)、人工神经网络(ANNs)和转录的一般速率定律(GRLOT)方法。根据它们在不同条件下复制参考模型的调节结构和动态基因表达行为的能力,对这些方法进行了彻底的评估。
虽然 ANN 和 GRLOT 方法似乎即使在模型参数与参考模型有很大偏差的情况下也能产生稳健的模型,但基于 SS 的模型即使反向工程模型的参数与参考模型非常接近时,性能也会显著下降:这是由于 SS 方法中的幂次项数量多,以及它们的组合方式。在跨方法反向工程实验中,揭示了方法的不同特征、偏差和特点。基于有限的训练数据,只有一个实验条件,所有方法都生成了能够准确复制训练数据的动态模型。然而,只有在多个实验条件下的训练数据才能实现对调控网络特征的准确再现。
所研究的 GRN 建模方法生成的动态 GRN 模型在复制参考模型的结构和行为方面表现出显著差异。我们的结果表明,在选择特定应用的方法时应谨慎。特别是,仅依赖一种方法可能会不适当地偏倚结果。