Evaluation of predicted network modules in yeast metabolism using NMR-based metabolite profiling

被引:58
作者
Bundy, Jacob G.
Papp, Balazs
Harmston, Rebecca
Browne, Roy A.
Clayson, Edward M.
Burton, Nicola
Reece, Richard J.
Oliver, Stephen G.
Brindle, Kevin M. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[2] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
D O I
10.1101/gr.5662207
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genome-scale metabolic models promise important insights into cell function. However, the definition of pathways and functional network modules within these models, and in the biochemical literature in general, is often based on intuitive reasoning. Although mathematical methods have been proposed to identify modules, which are defined as groups of reactions with correlated fluxes, there is a need for experimental verification. We show here that multivariate statistical analysis of the NMR-derived intra- and extracellular metabolite profiles of single-gene deletion mutants in specific metabolic pathways in the yeast Saccharomyces cerevisiae identified outliers whose profiles were markedly different from those of the other mutants in their respective pathways. Application of flux coupling analysis to a metabolic model of this yeast showed that the deleted gene in an outlying mutant encoded an enzyme that was not part of the same functional network module as the other enzymes in the pathway. We suggest that metabolomic methods such as this, which do not require any knowledge of how a gene deletion might perturb the metabolic network, provide an empirical method for validating and ultimately refining the predicted network structure.
引用
收藏
页码:510 / 519
页数:10
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