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Prediction of signaling networks by information propagation on protein-protein interaction networks integrated with GO annotations

机译:通过与GO注释集成的蛋白质-蛋白质相互作用网络上的信息传播来预测信号网络

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The experimental study of signal transduction over a decade has made a substantial contribution to understanding functional mechanisms in a cell. A signaling pathway represents a linear path of a signaling cascade involving a series of proteins. As an advanced model, multiple linear pathways with extensive cross-talk between receptors can be merged into a larger-scale signaling network. We present an efficient computational approach to predict signaling networks by integration of genome-wide protein-protein interaction (PPI) data and ontological annotation data. We adopt an advanced semantic similarity metric for weighting PPIs, and an information propagation algorithm that runs on a weighted PPI network. This algorithm iteratively selects potential directed edges for signaling cascade using user-specified path strength parameters. Our approach also includes a preprocessing step to filter the large-scale PPI network by distance condition using the maximum path length parameter. Our experimental results show that the proposed approach runs extremely faster than existing computational methods and has competitive accuracy in the test of predicting well-studied pathways of S. cerevisiae and C. elegans. High efficiency of this approach would facilitate development of a web-based application tool to discover potential signaling networks.
机译:十年来信号转导的实验研究为理解细胞的功能机制做出了重大贡献。信号传导途径代表涉及一系列蛋白质的信号传导级联的线性路径。作为高级模型,可以将在受体之间具有广泛串扰的多个线性路径合并为一个更大的信号网络。我们提出了一种有效的计算方法,通过整合全基因组范围的蛋白质-蛋白质相互作用(PPI)数据和本体注释数据来预测信号网络。我们对PPI加权采用高级语义相似性度量,并在加权PPI网络上运行信息传播算法。该算法使用用户指定的路径强度参数迭代选择潜在的有向边,以进行信号级联。我们的方法还包括一个预处理步骤,以使用最大路径长度参数按距离条件对大型PPI网络进行过滤。我们的实验结果表明,所提出的方法比现有的计算方法运行速度极快,并且在预测酿酒酵母和秀丽隐杆线虫的途径研究中具有竞争性的准确性。这种方法的高效率将促进基于Web的应用程序工具的开发,以发现潜在的信令网络。

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