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基于蛋白质-蛋白质相互作用网络预测参与肾小球疾病的关键细胞骨架成分

The Prediction of Key Cytoskeleton Components Involved in Glomerular Diseases Based on a Protein-Protein Interaction Network.

作者信息

Ding Fangrui, Tan Aidi, Ju Wenjun, Li Xuejuan, Li Shao, Ding Jie

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing, China.

MOE Key Laboratory of Bioinformatics and Bioinformatics Division, TNLIST, Department of Automation, Tsinghua University, Beijing, China.

出版信息

PLoS One. 2016 May 26;11(5):e0156024. doi: 10.1371/journal.pone.0156024. eCollection 2016.

Abstract

Maintenance of the physiological morphologies of different types of cells and tissues is essential for the normal functioning of each system in the human body. Dynamic variations in cell and tissue morphologies depend on accurate adjustments of the cytoskeletal system. The cytoskeletal system in the glomerulus plays a key role in the normal process of kidney filtration. To enhance the understanding of the possible roles of the cytoskeleton in glomerular diseases, we constructed the Glomerular Cytoskeleton Network (GCNet), which shows the protein-protein interaction network in the glomerulus, and identified several possible key cytoskeletal components involved in glomerular diseases. In this study, genes/proteins annotated to the cytoskeleton were detected by Gene Ontology analysis, and glomerulus-enriched genes were selected from nine available glomerular expression datasets. Then, the GCNet was generated by combining these two sets of information. To predict the possible key cytoskeleton components in glomerular diseases, we then examined the common regulation of the genes in GCNet in the context of five glomerular diseases based on their transcriptomic data. As a result, twenty-one cytoskeleton components as potential candidate were highlighted for consistently down- or up-regulating in all five glomerular diseases. And then, these candidates were examined in relation to existing known glomerular diseases and genes to determine their possible functions and interactions. In addition, the mRNA levels of these candidates were also validated in a puromycin aminonucleoside(PAN) induced rat nephropathy model and were also matched with existing Diabetic Nephropathy (DN) transcriptomic data. As a result, there are 15 of 21 candidates in PAN induced nephropathy model were consistent with our predication and also 12 of 21 candidates were matched with differentially expressed genes in the DN transcriptomic data. By providing a novel interaction network and prediction, GCNet contributes to improving the understanding of normal glomerular function and will be useful for detecting target cytoskeleton molecules of interest that may be involved in glomerular diseases in future studies.

摘要

维持不同类型细胞和组织的生理形态对于人体各系统的正常运作至关重要。细胞和组织形态的动态变化依赖于细胞骨架系统的精确调控。肾小球中的细胞骨架系统在肾脏滤过的正常过程中起关键作用。为了加深对细胞骨架在肾小球疾病中可能作用的理解,我们构建了肾小球细胞骨架网络(GCNet),该网络展示了肾小球中的蛋白质 - 蛋白质相互作用网络,并鉴定了几种可能参与肾小球疾病的关键细胞骨架成分。在本研究中,通过基因本体分析检测注释到细胞骨架的基因/蛋白质,并从九个可用的肾小球表达数据集中选择肾小球富集基因。然后,通过整合这两组信息生成GCNet。为了预测肾小球疾病中可能的关键细胞骨架成分,我们基于其转录组数据,在五种肾小球疾病的背景下研究了GCNet中基因的共同调控。结果表明,在所有五种肾小球疾病中持续下调或上调的二十一种细胞骨架成分被突出显示为潜在候选物。然后,将这些候选物与现有的已知肾小球疾病和基因相关联进行研究,以确定它们可能的功能和相互作用。此外,这些候选物的mRNA水平也在嘌呤霉素氨基核苷(PAN)诱导的大鼠肾病模型中得到验证,并且还与现有的糖尿病肾病(DN)转录组数据进行了匹配。结果,在PAN诱导的肾病模型中,21种候选物中有15种与我们的预测一致,并且在DN转录组数据中,21种候选物中有12种与差异表达基因匹配。通过提供一个新的相互作用网络和预测,GCNet有助于增进对正常肾小球功能的理解,并将有助于在未来研究中检测可能参与肾小球疾病的目标细胞骨架分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2570/4882061/c6095a88d5fc/pone.0156024.g001.jpg

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