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Identification of functional hubs and modules by converting interactome networks into hierarchical ordering of proteins

机译:通过将相互作用基因组网络转换成蛋白质的层次顺序来识别功能中心和模块

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Background Protein-protein interactions play a key role in biological processes of proteins within a cell. Recent high-throughput techniques have generated protein-protein interaction data in a genome-scale. A wide range of computational approaches have been applied to interactome network analysis for uncovering functional organizations and pathways. However, they have been challenged because ofcomplex connectivity. It has been investigated that protein interaction networks are typically characterized by intrinsic topological features: high modularity and hub-oriented structure. Elucidating the structural roles of modules and hubs is a critical step in complex interactome network analysis. Results We propose a novel approach to convert the complex structure of an interactome network into hierarchical ordering of proteins. This algorithm measures functional similarity between proteins based on the path strength model, and reveals a hub-oriented tree structure hidden in the complex network. We score hub confidence and identify functional modules in the tree structure of proteins, retrieved by our algorithm. Our experimental results in the yeast protein interactome network demonstrate that the selected hubs are essential proteins for performing functions. In network topology, they have a role in bridging different functional modules. Furthermore, our approach has high accuracy in identifying functional modules hierarchically distributed. Conclusions Decomposing, converting, and synthesizing complex interaction networks are fundamental tasks for modeling their structural behaviors. In this study, we systematically analyzed complex interactome network structures for retrievingfunctional information. Unlike previous hierarchical clustering methods, this approach dynamically explores the hierarchical structure of proteins in a global view. It is well-applicable to the interactome networks in high-level organisms because of its efficiency and scalability.
机译:背景技术蛋白质-蛋白质相互作用在细胞内蛋白质的生物学过程中起关键作用。最近的高通量技术已经产生了基因组规模的蛋白质-蛋白质相互作用数据。广泛的计算方法已应用于交互组网络分析,以发现功能组织和途径。但是,它们由于复杂的连接性而受到挑战。已经研究出蛋白质相互作用网络通常以固有的拓扑特征为特征:高模块性和面向集线器的结构。阐明模块和集线器的结构作用是复杂的交互组网络分析中的关键步骤。结果我们提出了一种新颖的方法来将一个相互作用组网络的复杂结构转换为蛋白质的层次顺序。该算法基于路径强度模型测量蛋白质之间的功能相似性,并揭示隐藏在复杂网络中的面向集线器的树结构。我们对集线器置信度评分,并确定蛋白质树结构中的功能模块,这些蛋白质是通过我们的算法检索得到的。我们在酵母蛋白质相互作用组网络中的实验结果表明,所选集线器是执行功能所必需的蛋白质。在网络拓扑中,它们在桥接不同的功能模块中起作用。此外,我们的方法在识别分层分布的功能模块方面具有很高的准确性。结论分解,转换和综合复杂的交互网络是建模其结构行为的基本任务。在这项研究中,我们系统地分析了复杂的相互作用组网络结构以检索功能信息。与以前的层次聚类方法不同,此方法可在全局视图中动态探索蛋白质的层次结构。由于它的效率和可扩展性,它非常适用于高级生物中的交互组网络。

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