Path to improving the life cycle and quality of genome-scale models of metabolism

被引:15
作者
Seif, Yara [1 ,2 ]
Palsson, Bernhard Orn [1 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92093 USA
[2] Merck & Co Inc, San Francisco, CA 94080 USA
关键词
STAPHYLOCOCCUS-AUREUS; ESCHERICHIA-COLI; METACYC DATABASE; SYSTEMS BIOLOGY; GLOBAL RECONSTRUCTION; BIOCYC COLLECTION; GENE ESSENTIALITY; SWISS-PROT; NETWORK; ENZYMES;
D O I
10.1016/j.cels.2021.06.005
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 models of metabolism (GEMs) are key computational tools for the systems-level study of metabolic networks. Here, we describe the "GEM life cycle," which we subdivide into four stages: inception, maturation, specialization, and amalgamation. We show how different types of GEM reconstruction work-flows fit in each stage and proceed to highlight two fundamental bottlenecks for GEM quality improvement: GEM maturation and content removal. We identify common characteristics contributing to increasing quality of maturing GEMs drawing from past independent GEM maturation efforts. We then shed some much-needed light on the latent and unrecognized but pervasive issue of content removal, demonstrating the substantial effects of model pruning on its solution space. Finally, we propose a novel framework for content removal and associated confidence-level assignment which will help guide future GEM development efforts, reduce duplication of effort across groups, potentially aid automated reconstruction platforms, and boost the reproducibility of model development.
引用
收藏
页码:842 / 859
页数:18
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