Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093-0412, USA and Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Bioinformatics. 2013 Nov 15;29(22):2900-8. doi: 10.1093/bioinformatics/btt493. Epub 2013 Aug 23.
Genome-scale metabolic models have been used extensively to investigate alterations in cellular metabolism. The accuracy of these models to represent cellular metabolism in specific conditions has been improved by constraining the model with omics data sources. However, few practical methods for integrating metabolomics data with other omics data sources into genome-scale models of metabolism have been developed.
GIM(3)E (Gene Inactivation Moderated by Metabolism, Metabolomics and Expression) is an algorithm that enables the development of condition-specific models based on an objective function, transcriptomics and cellular metabolomics data. GIM(3)E establishes metabolite use requirements with metabolomics data, uses model-paired transcriptomics data to find experimentally supported solutions and provides calculations of the turnover (production/consumption) flux of metabolites. GIM(3)E was used to investigate the effects of integrating additional omics datasets to create increasingly constrained solution spaces of Salmonella Typhimurium metabolism during growth in both rich and virulence media. This integration proved to be informative and resulted in a requirement of additional active reactions (12 in each case) or metabolites (26 or 29, respectively). The addition of constraints from transcriptomics also impacted the allowed solution space, and the cellular metabolites with turnover fluxes that were necessarily altered by the change in conditions increased from 118 to 271 of 1397.
GIM(3)E has been implemented in Python and requires a COBRApy 0.2.x. The algorithm and sample data described here are freely available at: http://opencobra.sourceforge.net/
基因组规模的代谢模型已被广泛用于研究细胞代谢的变化。通过将模型与组学数据源约束,可以提高这些模型在特定条件下代表细胞代谢的准确性。然而,将代谢组学数据与其他组学数据源集成到代谢的基因组规模模型中的实用方法很少。
GIM(3)E(受代谢、代谢组学和表达调节的基因失活)是一种算法,它可以根据目标函数、转录组学和细胞代谢组学数据开发特定条件的模型。GIM(3)E 使用代谢组学数据建立代谢物使用要求,使用模型配对转录组学数据找到经过实验支持的解决方案,并提供代谢物周转率(产生/消耗)通量的计算。GIM(3)E 用于研究在丰富和毒力培养基中生长时,整合其他组学数据集以创建越来越受限制的沙门氏菌 Typhimurium 代谢解决方案空间的影响。这种整合被证明是有益的,并导致需要额外的活跃反应(每种情况下 12 个)或代谢物(分别为 26 或 29 个)。转录组学约束的增加也会影响允许的解决方案空间,并且由于条件变化而必然改变的细胞代谢物的周转率通量从 1397 个中的 118 个增加到 271 个。
GIM(3)E 已在 Python 中实现,并且需要 COBRApy 0.2.x。这里描述的算法和示例数据可在以下网址免费获得:http://opencobra.sourceforge.net/