Abstract

BackgroundMicroarray technology produces gene expression data on a genomic scale for an endless variety of organisms and conditions. However, this vast amount of information needs to be extracted in a reasonable way and funneled into manageable and functionally meaningful patterns. Genes may be reasonably combined using knowledge about their interaction behaviour. On a proteomic level, biochemical research has elucidated an increasingly complete image of the metabolic architecture, especially for less complex organisms like the well studied bacterium Escherichia coli.ResultsWe sought to discover central components of the metabolic network, regulated by the expression of associated genes under changing conditions. We mapped gene expression data from E. coli under aerobic and anaerobic conditions onto the enzymatic reaction nodes of its metabolic network. An adjacency matrix of the metabolites was created from this graph. A consecutive ones clustering method was used to obtain network clusters in the matrix. The wavelet method was applied on the adjacency matrices of these clusters to collect features for the classifier. With a feature extraction method the most discriminating features were selected. We yielded network sub-graphs from these top ranking features representing formate fermentation, in good agreement with the anaerobic response of hetero-fermentative bacteria. Furthermore, we found a switch in the starting point for NAD biosynthesis, and an adaptation of the l-aspartate metabolism, in accordance with its higher abundance under anaerobic conditions.ConclusionWe developed and tested a novel method, based on a combination of rationally chosen machine learning methods, to analyse gene expression data on the basis of interaction data, using a metabolic network of enzymes. As a case study, we applied our method to E. coli under oxygen deprived conditions and extracted physiologically relevant patterns that represent an adaptation of the cells to changing environmental conditions. In general, our concept may be transferred to network analyses on biological interaction data, when data for two comparable states of the associated nodes are made available.

Highlights

  • Microarray technology produces gene expression data on a genomic scale for an endless variety of organisms and conditions

  • Over the last 40 years, biochemical investigations have discovered an increasingly consistent image of cellular metabolism. This is especially true for less complex organisms such as Escherichia coli [2]

  • We investigated the response of the hetero-fermentative bacterium E. coli in response to oxygen deprivation

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Summary

Introduction

Microarray technology produces gene expression data on a genomic scale for an endless variety of organisms and conditions. This is especially true for less complex organisms such as Escherichia coli [2] This alone provides a rather static image of the cell and investigations have been performed to discover cellular adaptation programs in response to changing environments such as nutrient excess, starvation and other stresses [3]. These observations originally followed rather linear interaction and reaction cascades, e.g. by investigating single knock-outs and tediously tracking of transcripts for single genes, or compounds and proteins that may potentially be influenced Interaction knowledge from the biochemical network has been used to support the clustering procedure for gene expression profiles of yeast [12,13]

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