ArticleBMC bioinformatics2010
Identification of functional hubs and modules by converting interactome networks into hierarchical ordering of proteins.
Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed.
- Global temporal dynamic landscape of pathogen-mediated subversion of Arabidopsis innate immunity.Scientific reports · 2017Article
- Article
- Improving biomarker list stability by integration of biological knowledge in the learning process.BMC bioinformatics · 2012Article
- HomPPI: a class of sequence homology based protein-protein interface prediction methods.BMC bioinformatics · 2011Article
- Exploring hierarchical and overlapping modular structure in the yeast protein interaction network.BMC genomics · 2010Article
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2 authors.
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Abstract
backgroundProtein-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 of complex 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.
resultsWe 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.
conclusionsDecomposing, 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 retrieving functional 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.
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