Abstract

One of the main challenges of the post-genomic era is the understanding of how gene expression is controlled. Changes in gene expression lay behind diverse biological phenomena such as development, disease and the adaptation to different environmental conditions. Despite the availability of well-established methods to identify these changes, tools to discern how gene regulation is orchestrated are still required. The regulation of gene expression is usually depicted as a Gene Regulatory Network (GRN) where changes in the network structure (i.e., network topology) represent adjustments of gene regulation. Like other networks, GRNs are composed of basic building blocks; small induced subgraphs called graphlets. Here we present LoTo, a novel method that using Graphlet Based Metrics (GBMs) identifies topological variations between different states of a GRN. Under our approach, different states of a GRN are analyzed to determine the types of graphlet formed by all triplets of nodes in the network. Subsequently, graphlets occurring in a state of the network are compared to those formed by the same three nodes in another version of the network. Once the comparisons are performed, LoTo applies metrics from binary classification problems calculated on the existence and absence of graphlets to assess the topological similarity between both network states. Experiments performed on randomized networks demonstrate that GBMs are more sensitive to topological variation than the same metrics calculated on single edges. Additional comparisons with other common metrics demonstrate that our GBMs are capable to identify nodes whose local topology changes between different states of the network. Notably, due to the explicit use of graphlets, LoTo captures topological variations that are disregarded by other approaches. LoTo is freely available as an online web server at http://dlab.cl/loto.

Highlights

  • In biological sciences, networks are becoming one of the main tools to study complex systems (Newman, 2010)

  • Graphlet characterization of Gene Regulatory Network (GRN) Characterization of the RegulonDB gold standard Starting from RegulonDB version 8.7, a gold standard GRN was built

  • This GRN is formed by 1,805 genes, of which 202 encode for Transcription Factor (TF), and 4,511 true edges

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Summary

Introduction

Networks are becoming one of the main tools to study complex systems (Newman, 2010). GRNs are directed networks where nodes represent genes, and the links between nodes exist solely if the regulatory element, e.g., a Transcription Factor (TF), encoded by a source gene directly regulates the expression of another target gene. Major applications of GRNs are intended to perform differential studies in which diverse states of a network representing the same biological system are compared (Davidson et al, 2002; Shiozaki et al, 2011; Yang & Wu, 2012; Cheng, Sun & Socolar, 2013; Gaiteri et al, 2014; Okawa et al, 2015). Network properties that can be used to compare networks and to asses their structural difference include the distribution of connections versus non-connections (density), diameter, size/order, connectedness, betweenness, centrality and the distribution of node degree (Newman, 2010)

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