Abstract

BackgroundMessenger RNA expression is regulated by a complex interplay of different regulatory proteins. Unfortunately, directly measuring the individual activity of these regulatory proteins is difficult, leaving us with only the resulting gene expression pattern as a marker for the underlying regulatory network or regulator-gene associations. Furthermore, traditional methods to predict these regulator-gene associations do not define the relative importance of each association, leading to a large number of connections in the global regulatory network that, although true, are not useful.ResultsHere we present a Bayesian method that identifies which known transcriptional relationships in a regulatory network are consistent with a given body of static gene expression data by eliminating the non-relevant ones. The Partially Observed Bipartite Network (POBN) approach developed here is tested using E. coli expression data and a transcriptional regulatory network derived from RegulonDB. When the regulatory network for E. coli was integrated with 266 E. coli gene chip observations, POBN identified 93 out of 570 connections that were either inconsistent or not adequately supported by the expression data.ConclusionPOBN provides a systematic way to integrate known transcriptional networks with observed gene expression data to better identify which transcriptional pathways are likely responsible for the observed gene expression pattern.

Highlights

  • Messenger RNA expression is regulated by a complex interplay of different regulatory proteins

  • The bioinformatics community has collected many of these gene-gene regulatory relationships into transcriptional networks that provide a global view of how gene regulation is orchestrated

  • To test the performance of the Partially Observed Bipartite Network (POBN) algorithm for regulatory network reconstruction, we focus on the regulatory networks in E. coli

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Summary

Introduction

Messenger RNA expression is regulated by a complex interplay of different regulatory proteins. TRANSFAC collects protein-DNA binding interactions to identify potential gene regulatory mechanisms [4]. Some gene regulatory mechanisms may only be used in rare cases of stress, or during a short developmental stage. In these cases, these rarely used regulatory mechanisms are correct, but largely non-predictive and as such may not be relevant to the process under study. These rarely used regulatory mechanisms are correct, but largely non-predictive and as such may not be relevant to the process under study In these specific cases, the general regulatory network is less useful

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