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General Interest: Data integration in physiology using Bayes’ rule and minimum Bayes’ factors: deubiquitylating enzymes in the renal collecting duct

机译:一般兴趣:使用贝叶斯法则和最小贝叶斯因数的生理数据集成:肾脏收集管中的泛素化酶

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摘要

A major challenge in physiology is to exploit the many large-scale data sets available from “-omic” studies to seek answers to key physiological questions. In previous studies, Bayes’ theorem has been used for this purpose. This approach requires a means to map continuously distributed experimental data to probabilities (likelihood values) to derive posterior probabilities from the combination of prior probabilities and new data. Here, we introduce the use of minimum Bayes’ factors for this purpose and illustrate the approach by addressing a physiological question, “Which deubiquitylating enzymes (DUBs) encoded by mammalian genomes are most likely to regulate plasma membrane transport processes in renal cortical collecting duct principal cells?” To do this, we have created a comprehensive online database of 110 DUBs present in the mammalian genome (). We used Bayes’ theorem to integrate available information from large-scale data sets derived from proteomic and transcriptomic studies of renal collecting duct cells to rank the 110 known DUBs with regard to likelihood of interacting with and regulating transport processes. The top-ranked DUBs were OTUB1, USP14, PSMD7, PSMD14, USP7, USP9X, OTUD4, USP10, and UCHL5. Among these USP7, USP9X, OTUD4, and USP10 are known to be involved in endosomal trafficking and have potential roles in endosomal recycling of plasma membrane proteins in the mammalian cortical collecting duct.
机译:生理学的主要挑战是利用“-组学”研究中可用的许多大规模数据集来寻找关键生理问题的答案。在先前的研究中,贝叶斯定理已用于此目的。这种方法需要一种将连续分布的实验数据映射到概率(似然值)的方法,以从先验概率和新数据的组合得出后验概率。在这里,我们介绍了为此目的使用最小贝叶斯因子的方法,并通过解决一个生理问题来说明该方法:“由哺乳动物基因组编码的去泛素化酶(DUB)最有可能调节肾皮质收集管中的质膜转运过程细胞?”为此,我们创建了一个完整的在线数据库,其中包含哺乳动物基因组()中的110个DUB。我们使用贝叶斯定理对来自肾脏收集导管细胞的蛋白质组学和转录组学研究的大规模数据集的可用信息进行整合,以对110个已知的DUB进行交互作用并调节运输过程的可能性。排名最高的DUB是OTUB1,USP14,PSMD7,PSMD14,USP7,USP9X,OTUD4,USP10和UCHL5。在这些USP7,USP9X,OTUD4和USP10中,已知参与内体运输,并且在哺乳动物皮质收集管中内质膜蛋白的内体回收中具有潜在作用。

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