Abstract

BackgroundA key challenge in the post genome era is to identify genome-wide transcriptional regulatory networks, which specify the interactions between transcription factors and their target genes. Numerous methods have been developed for reconstructing gene regulatory networks from expression data. However, most of them are based on coarse grained qualitative models, and cannot provide a quantitative view of regulatory systems.ResultsA binding affinity based regulatory model is proposed to quantify the transcriptional regulatory network. Multiple quantities, including binding affinity and the activity level of transcription factor (TF) are incorporated into a general learning model. The sequence features of the promoter and the possible occupancy of nucleosomes are exploited to estimate the binding probability of regulators. Comparing with the previous models that only employ microarray data, the proposed model can bridge the gap between the relative background frequency of the observed nucleotide and the gene's transcription rate.ConclusionsWe testify the proposed approach on two real-world microarray datasets. Experimental results show that the proposed model can effectively identify the parameters and the activity level of TF. Moreover, the kinetic parameters introduced in the proposed model can reveal more biological sense than previous models can do.

Highlights

  • A key challenge in the post genome era is to identify genome-wide transcriptional regulatory networks, which specify the interactions between transcription factors and their target genes

  • There are two broad classes of gene regulatory interactions: one based on the ‘physical interaction’ that aim at identifying relationships among transcription factors and their target genes and another based on the ‘influence interaction’ that try to relate the expression of a gene to the expression of the other genes in the cell

  • transcription factor (TF)’ activity levels are difficult to measure mainly due to two technical limitations: TFs are often present at low intercellular concentrations and the changes in their activity state can occur rapidly due to post-translational modifications

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Summary

Introduction

A key challenge in the post genome era is to identify genome-wide transcriptional regulatory networks, which specify the interactions between transcription factors and their target genes. Researchers have proposed many different computational approaches to reconstruct gene regulatory networks from high-throughput data, e.g. see reviews by Bansal et al and Markowetz and Spang [1,2] These approaches fall roughly into two categories: qualitative and quantitative aspects. Inferring qualitative regulatory networks from microarray data has been well studied, and a number of effective approaches have been developed [3,4,5,6,7,8,9,10] These methods are based on coarse grained qualitative models [11,12], and cannot provide a realistic and quantitative view of regulatory systems. TFs’ activity levels are difficult to measure mainly due to two technical limitations: TFs are often present at low intercellular concentrations and the changes in their activity state can occur rapidly due to post-translational modifications

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