Research

Model-driven analysis of experimentally determined growth phenotypes for 465 yeast gene deletion mutants under 16 different conditions

Evan S Snitkin¹ , Aimée M Dudley² , Daniel M Janse³ , Kaisheen Wong^{^} , George M Church⁴ and Daniel Segrè^1,5

¹  Bioinformatics graduate Program, Boston University, Boston, MA 02215, USA

²  Institute for Systems Biology, Seattle, WA 98103, USA

³  McKinsey & Company, London, SW1Y 4UH, UK

⁴  Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA

⁵  Departments of Biology and Biomedical Engineering, Boston University, Boston, MA, 02215, USA

author email corresponding author email^Deceased

Genome Biology 2008, 9:R140doi:10.1186/gb-2008-9-9-r140

Published:	22 September 2008

Subject areas: Biochemistry and structural biology, Bioinformatics, Microbiology and parasitology, Model organisms, Physiology

Abstract

Background

Understanding the response of complex biochemical networks to genetic perturbations and environmental variability is a fundamental challenge in biology. Integration of high-throughput experimental assays and genome-scale computational methods is likely to produce insight otherwise unreachable, but specific examples of such integration have only begun to be explored.

Results

In this study, we measured growth phenotypes of 465 Saccharomyces cerevisiae gene deletion mutants under 16 metabolically relevant conditions and integrated them with the corresponding flux balance model predictions. We first used discordance between experimental results and model predictions to guide a stage of experimental refinement, which resulted in a significant improvement in the quality of the experimental data. Next, we used discordance still present in the refined experimental data to assess the reliability of yeast metabolism models under different conditions. In addition to estimating predictive capacity based on growth phenotypes, we sought to explain these discordances by examining predicted flux distributions visualized through a new, freely available platform. This analysis led to insight into the glycerol utilization pathway and the potential effects of metabolic shortcuts on model results. Finally, we used model predictions and experimental data to discriminate between alternative raffinose catabolism routes.

Conclusions

Our study demonstrates how a new level of integration between high throughput measurements and flux balance model predictions can improve understanding of both experimental and computational results. The added value of a joint analysis is a more reliable platform for specific testing of biological hypotheses, such as the catabolic routes of different carbon sources.