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NIBBS-Search for Fast and Accurate Prediction of Phenotype-Biased Metabolic Systems

机译:NIBBS-搜索快速准确地预测表型代谢系统

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摘要

Understanding of genotype-phenotype associations is important not only for furthering our knowledge on internal cellular processes, but also essential for providing the foundation necessary for genetic engineering of microorganisms for industrial use (e.g., production of bioenergy or biofuels). However, genotype-phenotype associations alone do not provide enough information to alter an organism's genome to either suppress or exhibit a phenotype. It is important to look at the phenotype-related genes in the context of the genome-scale network to understand how the genes interact with other genes in the organism. Identification of metabolic subsystems involved in the expression of the phenotype is one way of placing the phenotype-related genes in the context of the entire network. A metabolic system refers to a metabolic network subgraph; nodes are compounds and edges labels are the enzymes that catalyze the reaction. The metabolic subsystem could be part of a single metabolic pathway or span parts of multiple pathways. Arguably, comparative genome-scale metabolic network analysis is a promising strategy to identify these phenotype-related metabolic subsystems. Network Instance-Based Biased Subgraph Search (>NIBBS) is a graph-theoretic method for genome-scale metabolic network comparative analysis that can identify metabolic systems that are statistically biased toward phenotype-expressing organismal networks. We set up experiments with target phenotypes like hydrogen production, TCA expression, and acid-tolerance. We show via extensive literature search that some of the resulting metabolic subsystems are indeed phenotype-related and formulate hypotheses for other systems in terms of their role in phenotype expression. NIBBS is also orders of magnitude faster than MULE, one of the most efficient maximal frequent subgraph mining algorithms that could be adjusted for this problem. Also, the set of phenotype-biased metabolic systems output by NIBBS comes very close to the set of phenotype-biased subgraphs output by an exact maximally-biased subgraph enumeration algorithm ( MBS-Enum ). The code (NIBBS and the module to visualize the identified subsystems) is available at .
机译:了解基因型与表型之间的联系不仅对增进我们对内部细胞过程的了解很重要,而且对于为工业用微生物的基因工程(例如生产生物能源或生物燃料)提供必要的基础也至关重要。然而,单独的基因型-表型关联不能提供足够的信息来改变生物体的基因组以抑制或表现出表型。重要的是要在基因组规模网络的背景下查看与表型相关的基因,以了解这些基因如何与生物体中的其他基因相互作用。鉴定涉及表型表达的代谢子系统是将表型相关基因置于整个网络中的一种方法。代谢系统是指代谢网络子图;节点是化合物,边缘标记是催化反应的酶。代谢子系统可以是单个代谢途径的一部分,也可以是多个途径的一部分。可以说,比较基因组规模的代谢网络分析是鉴定这些表型相关代谢子系统的有前途的策略。基于网络实例的有偏子图搜索(> NIBBS )是一种用于图谱理论的基因组规模代谢网络比较分析方法,可以识别在统计学上偏向表型表达有机网络的代谢系统。我们针对目标表型(例如产氢量,TCA表达和耐酸性)进行了实验。我们通过大量的文献研究表明,某些产生的代谢子系统确实与表型有关,并就其他系统在表型表达中的作用提出了假设。 NIBBS也比MULE快几个数量级,MULE是可以针对此问题进行调整的最有效的最大频繁子图挖掘算法之一。同样,NIBBS输出的表型偏差代谢系统集与精确的最大偏差子图枚举算法(MBS-Enum)输出的表型偏差子图集非常接近。该代码(NIBBS和用于可视化所标识子系统的模块)位于。

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