Framework for network modularization and Bayesian network analysis to investigate the perturbed metabolic network

被引:13
|
作者
Kim, Hyun Uk [1 ,2 ]
Kim, Tae Yong [1 ,2 ]
Lee, Sang Yup [1 ,2 ,3 ,4 ]
机构
[1] Korea Adv Inst Sci & Technol, Inst BioCentury, Ctr Syst & Synthet Biotechnol,Program BK21, Dept Chem & Biomol Engn,Metab & Biomol Engn Natl, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, BioInformat Res Ctr, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[4] Korea Adv Inst Sci & Technol, BioProc Engn Res Ctr, Taejon 305701, South Korea
来源
BMC SYSTEMS BIOLOGY | 2011年 / 5卷
关键词
ESCHERICHIA-COLI; FLUX ANALYSIS; BIOLOGY; RECONSTRUCTIONS; ORGANIZATION; TARGETS; QUALITY; PROTEIN;
D O I
10.1186/1752-0509-5-S2-S14
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Genome-scale metabolic network models have contributed to elucidating biological phenomena, and predicting gene targets to engineer for biotechnological applications. With their increasing importance, their precise network characterization has also been crucial for better understanding of the cellular physiology. Results: We herein introduce a framework for network modularization and Bayesian network analysis (FMB) to investigate organism's metabolism under perturbation. FMB reveals direction of influences among metabolic modules, in which reactions with similar or positively correlated flux variation patterns are clustered, in response to specific perturbation using metabolic flux data. With metabolic flux data calculated by constraints-based flux analysis under both control and perturbation conditions, FMB, in essence, reveals the effects of specific perturbations on the biological system through network modularization and Bayesian network analysis at metabolic modular level. As a demonstration, this framework was applied to the genetically perturbed Escherichia coli metabolism, which is a lpdA gene knockout mutant, using its genome-scale metabolic network model. Conclusions: After all, it provides alternative scenarios of metabolic flux distributions in response to the perturbation, which are complementary to the data obtained from conventionally available genome-wide high-throughput techniques or metabolic flux analysis.
引用
收藏
页数:12
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