Abstract

BackgroundComparative analysis of protein-protein interaction (PPI) networks provides an effective means of detecting conserved functional network modules across different species. Such modules typically consist of orthologous proteins with conserved interactions, which can be exploited to computationally predict the modules through network comparison.ResultsIn this work, we propose a novel probabilistic framework for comparing PPI networks and effectively predicting the correspondence between proteins, represented as network nodes, that belong to conserved functional modules across the given PPI networks. The basic idea is to estimate the steady-state network flow between nodes that belong to different PPI networks based on a Markov random walk model. The random walker is designed to make random moves to adjacent nodes within a PPI network as well as cross-network moves between potential orthologous nodes with high sequence similarity. Based on this Markov random walk model, we estimate the steady-state network flow – or the long-term relative frequency of the transitions that the random walker makes – between nodes in different PPI networks, which can be used as a probabilistic score measuring their potential correspondence. Subsequently, the estimated scores can be used for detecting orthologous proteins in conserved functional modules through network alignment.ConclusionsThrough evaluations based on multiple real PPI networks, we demonstrate that the proposed scheme leads to improved alignment results that are biologically more meaningful at reduced computational cost, outperforming the current state-of-the-art algorithms. The source code and datasets can be downloaded from http://www.ece.tamu.edu/~bjyoon/CUFID.

Highlights

  • Comparative analysis of protein-protein interaction (PPI) networks provides an effective means of detecting conserved functional network modules across different species

  • We assessed the quality of the predicted network alignment based on the following metrics: correct nodes (CN), specificity (SPE), gene ontology consistency (GOC) scores, conserved interactions (CI), conserved orthologous interactions (COI), and computation time

  • Note that CN, SPE, and GOC scores assess the biological significance of the alignment, and CI and COI assess the topological quality of the alignment

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Summary

Introduction

Comparative analysis of protein-protein interaction (PPI) networks provides an effective means of detecting conserved functional network modules across different species Such modules typically consist of orthologous proteins with conserved interactions, which can be exploited to computationally predict the modules through network comparison. Thanks to recent advances in high-throughput protein interaction measurement techniques, PPI networks for different species have been archived in public databases, where the coverage and quality of these networks continue to improve over time To translate these protein interaction data into useful biological knowledge – for example, that of the functional organization of cells and the detailed mechanisms of various cellular functions – we need effective means for analyzing the available PPI networks to accurately annotate the protein functions. By identifying corresponding protein nodes across networks, functional annotations of known proteins in well-studied species could be transferred to matching proteins in the PPI networks of less-studied species, which provides an efficient way of predicting potential functions of unknown proteins

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