FUSE: Multiple Network Alignment via Data Fusion

TL;DR

FUSE is a novel method for multiple network alignment in systems biology that fuses topological and functional data across PPI networks to improve the identification of conserved biological modules.

Contribution

FUSE introduces a new approach combining Non-negative Matrix Tri-Factorization and a maximum weight k-partite matching algorithm for more comprehensive and efficient multiple network alignment.

Findings

FUSE finds more functionally conserved protein pairs than sequence similarity alone.

FUSE produces the largest number of functionally consistent clusters.

FUSE is more computationally efficient than existing methods.

Abstract

Discovering patterns in networks of protein-protein interactions (PPIs) is a central problem in systems biology. Alignments between these networks aid functional understanding as they uncover important information, such as evolutionary conserved pathways, protein complexes and functional orthologs. The objective of a multiple network alignment is to create clusters of nodes that are evolutionarily conserved and functionally consistent across all networks. Unfortunately, the alignment methods proposed thus far do not fully meet this objective, as they are guided by pairwise scores that do not utilize the entire functional and topological information across all networks. To overcome this weakness, we propose FUSE, a multiple network aligner that utilizes all functional and topological information in all PPI networks. It works in two steps. First, it computes novel similarity scores of proteins across the PPI networks by fusing from all aligned networks both the protein wiring patterns and their sequence similarities. It does this by using Non-negative Matrix Tri-Factorization (NMTF). When we apply NMTF on the five largest and most complete PPI networks from BioGRID, we show that NMTF finds a larger number of protein pairs across the PPI networks that are functionally conserved than can be found by using protein sequence similarities alone. This demonstrates complementarity of protein sequence and their wiring patterns in the PPI networks. In the second step, FUSE uses a novel maximum weight k-partite matching approximation algorithm to find an alignment between multiple networks. We compare FUSE with the state of the art multiple network aligners and show that it produces the largest number of functionally consistent clusters that cover all aligned PPI networks. Also, FUSE is more computationally efficient than other multiple network aligners.