Corcoran Callan C, Grady Cameron R, Pisitkun Trairak, Parulekar Jaya, Knepper Mark A
Epithelial Systems Biology Laboratory, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland; and.
Systems Biology Center, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Am J Physiol Renal Physiol. 2017 Mar 1;312(3):F533-F542. doi: 10.1152/ajprenal.00601.2016. Epub 2016 Dec 14.
The organization of the mammalian genome into gene subsets corresponding to specific functional classes has provided key tools for systems biology research. Here, we have created a web-accessible resource called the https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/MetabolicEnzymeDatabase.html) keyed to the biochemical reactions represented on iconic metabolic pathway wall charts created in the previous century. Overall, we have mapped 1,647 genes to these pathways, representing ~7 percent of the protein-coding genome. To illustrate the use of the database, we apply it to the area of kidney physiology. In so doing, we have created an additional database ( https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/), mapping mRNA abundance measurements (mined from RNA-Seq studies) for all metabolic enzymes to each of 14 renal tubule segments. We carry out bioinformatics analysis of the enzyme expression pattern among renal tubule segments and mine various data sources to identify vasopressin-regulated metabolic enzymes in the renal collecting duct.
哺乳动物基因组组织成对应特定功能类别的基因子集,为系统生物学研究提供了关键工具。在此,我们创建了一个可通过网络访问的资源(https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/MetabolicEnzymeDatabase.html),该资源与上世纪创建的标志性代谢途径挂图上所呈现的生化反应相关联。总体而言,我们已将1647个基因映射到这些途径,占蛋白质编码基因组的约7%。为说明该数据库的用途,我们将其应用于肾脏生理学领域。在此过程中,我们创建了另一个数据库(https://hpcwebapps.cit.nih.gov/ESBL/Database/MetabolicEnzymes/),将所有代谢酶的mRNA丰度测量值(从RNA测序研究中挖掘)映射到14个肾小管节段中的每一个。我们对肾小管节段间的酶表达模式进行生物信息学分析,并挖掘各种数据源以鉴定肾集合管中血管加压素调节的代谢酶。