Abstract
As increasing amounts of high-throughput data for the yeast interactome become available, more system-wide properties are uncovered. One interesting question concerns the fault tolerance of protein interaction networks: whether there exist alternative pathways that can perform some required function if a gene essential to the main mechanism is defective, absent or suppressed. A signature pattern for redundant pathways is the BPM (between-pathway model) motif, introduced by Kelley and Ideker. Past methods proposed to search the yeast interactome for BPM motifs have had several important limitations. First, they have been driven heuristically by local greedy searches, which can lead to the inclusion of extra genes that may not belong in the motif; second, they have been validated solely by functional coherence of the putative pathways using GO enrichment, making it difficult to evaluate putative BPMs in the absence of already known biological annotation. We introduce stable bipartite subgraphs, and show they form a clean and efficient way of generating meaningful BPMs which naturally discard extra genes included by local greedy methods. We show by GO enrichment measures that our BPM set outperforms previous work, covering more known complexes and functional pathways. Perhaps most importantly, since our BPMs are initially generated by examining the genetic-interaction network only, the location of edges in the protein-protein physical interaction network can then be used to statistically validate each candidate BPM, even with sparse GO annotation (or none at all). We uncover some interesting biological examples of previously unknown putative redundant pathways in such areas as vesicle-mediated transport and DNA repair.
Highlights
It is estimated that only 18% of the yeast genome consists of essential genes, meaning that if the gene is deleted, the resulting strain is not viable on rich media [1]
We show that between-pathway model (BPM) obtained from stable bipartite subgraphs show significant functional enrichment over Gene Ontology (GO) categories
Using a network containing the same set of genetic interaction (GI) and physical interaction (PI) edges as that explored by Kelley and Ideker, we find 602 BPMs covering 1,526 SL edges with 53.4% of the 60262 = 1204 putative functional pathways exhibiting GO enrichment; Kelley and Ideker reported 360 BPMs covering 687 SL edges with 34.9% of their 36062 = 720 putative pathways exhibiting GO enrichment
Summary
It is estimated that only 18% of the yeast genome consists of essential genes, meaning that if the gene is deleted, the resulting strain is not viable on rich media [1]. The second mechanism involves the existence of redundant metabolic pathways or regulatory networks; this is called ‘‘robustness’’ by Wagner [6]. A third mechanism involving a more global and diffuse relation among multiple genes across many pathways has been reported to occur [7]. There is only preliminary data on the relative importance of the three mechanisms – one study estimates that at least 25% of the gene deletions in yeast that have no phenotype involve the first mechanism of duplicate genes [8]
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