Literature DB >> 21172910

Functional integration of a metabolic network model and expression data without arbitrary thresholding.

Paul A Jensen1, Jason A Papin.   

Abstract

MOTIVATION: Flux balance analysis (FBA) has been used extensively to analyze genome-scale, constraint-based models of metabolism in a variety of organisms. The predictive accuracy of such models has recently been improved through the integration of high-throughput expression profiles of metabolic genes and proteins. However, extensions of FBA often require that such data be discretized a priori into sets of genes or proteins that are either 'on' or 'off'. This procedure requires selecting relatively subjective expression thresholds, often requiring several iterations and refinements to capture the expression dynamics and retain model functionality.
RESULTS: We present a method for mapping expression data from a set of environmental, genetic or temporal conditions onto a metabolic network model without the need for arbitrary expression thresholds. Metabolic Adjustment by Differential Expression (MADE) uses the statistical significance of changes in gene or protein expression to create a functional metabolic model that most accurately recapitulates the expression dynamics. MADE was used to generate a series of models that reflect the metabolic adjustments seen in the transition from fermentative- to glycerol-based respiration in Saccharomyces cerevisiae. The calculated gene states match 98.7% of possible changes in expression, and the resulting models capture functional characteristics of the metabolic shift. AVAILABILITY: MADE is implemented in Matlab and requires a mixed-integer linear program solver. Source code is freely available at http://www.bme.virginia.edu/csbl/downloads/.

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Mesh:

Year:  2010        PMID: 21172910      PMCID: PMC6276961          DOI: 10.1093/bioinformatics/btq702

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  22 in total

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6.  A genome-scale computational study of the interplay between transcriptional regulation and metabolism.

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Review 7.  Applications of genome-scale metabolic reconstructions.

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  85 in total

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Review 7.  Metabolic network modeling of microbial communities.

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9.  Metabolic network-based stratification of hepatocellular carcinoma reveals three distinct tumor subtypes.

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Review 10.  Analysis of omics data with genome-scale models of metabolism.

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