Abstract
BackgroundSignaling pathways can be reconstructed by identifying ‘effect types’ (i.e. activation/inhibition) of protein-protein interactions (PPIs). Effect types are composed of ‘directions’ (i.e. upstream/downstream) and ‘signs’ (i.e. positive/negative), thereby requiring directions as well as signs of PPIs to predict signaling events from PPI networks. Here, we propose a computational method for systemically annotating effect types to PPIs using relations between functional information of proteins.ResultsWe used regulates, positively regulates, and negatively regulates relations in Gene Ontology (GO) to predict directions and signs of PPIs. These relations indicate both directions and signs between GO terms so that we can project directions and signs between relevant GO terms to PPIs. Independent test results showed that our method is effective for predicting both directions and signs of PPIs. Moreover, our method outperformed a previous GO-based method that did not consider the relations between GO terms. We annotated effect types to human PPIs and validated several highly confident effect types against literature. The annotated human PPIs are available in Additional file 2 to aid signaling pathway reconstruction and network biology research.ConclusionsWe annotated effect types to PPIs by using regulates, positively regulates, and negatively regulates relations in GO. We demonstrated that those relations are effective for predicting not only signs, but also directions of PPIs. The usefulness of those relations suggests their potential applications to other types of interactions such as protein-DNA interactions.
Highlights
Signaling pathways can be reconstructed by identifying ‘effect types’ of protein-protein interactions (PPIs)
We trained two logistic regression models that predicted whether a directed PPI can act as activation and inhibition, respectively
Feature generation for predicting directions of PPIs For predicting directions of PPIs, we only considered the directions of regulation pairs; whether it is from p1 to p2, or from p2 to p1
Summary
Signaling pathways can be reconstructed by identifying ‘effect types’ (i.e. activation/inhibition) of protein-protein interactions (PPIs). Effect types are composed of ‘directions’ (i.e. upstream/downstream) and ‘signs’ (i.e. positive/negative), thereby requiring directions as well as signs of PPIs to predict signaling events from PPI networks. A cell reacts to stimuli through signaling pathways, in which proteins physically interact with each other to transmit signals. Abnormal signal transduction triggers aberrant biological processes that might result in diseases such as cancer [2,3,4,5]. To understand how such signals flow, various high-throughput experiments have been developed. By combining directions with signs, we can define activation/inhibition relationships of PPIs, which we call ‘effect types’
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