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人类蛋白质、功能和疾病网络的综合分析。

Integrative analysis of human protein, function and disease networks.

作者信息

Liu Wei, Wu Aiping, Pellegrini Matteo, Wang Xiaofan

机构信息

Department of Automation, Shanghai Jiao Tong University, Shanghai, 200240, China.

Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100080.

出版信息

Sci Rep. 2015 Sep 24;5:14344. doi: 10.1038/srep14344.

DOI:10.1038/srep14344
PMID:26399914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4585831/
Abstract

Protein-protein interaction (PPI) networks serve as a powerful tool for unraveling protein functions, disease-gene and disease-disease associations. However, a direct strategy for integrating protein interaction, protein function and diseases is still absent. Moreover, the interrelated relationships among these three levels are poorly understood. Here we present a novel systematic method to integrate protein interaction, function, and disease networks. We first identified topological modules in human protein interaction data using the network topological algorithm (NeTA) we previously developed. The resulting modules were then associated with functional terms using Gene Ontology to obtain functional modules. Finally, disease modules were constructed by associating the modules with OMIM and GWAS. We found that most topological modules have cohesive structure, significant pathway annotations and good modularity. Most functional modules (70.6%) fully cover corresponding topological modules, and most disease modules (88.5%) are fully covered by the corresponding functional modules. Furthermore, we identified several protein modules of interest that we describe in detail, which demonstrate the power of our integrative approach. This approach allows us to link genes, and pathways with their corresponding disorders, which may ultimately help us to improve the prevention, diagnosis and treatment of disease.

摘要

蛋白质-蛋白质相互作用(PPI)网络是揭示蛋白质功能、疾病基因和疾病-疾病关联的有力工具。然而,整合蛋白质相互作用、蛋白质功能和疾病的直接策略仍然缺乏。此外,这三个层面之间的相互关系还知之甚少。在此,我们提出一种整合蛋白质相互作用、功能和疾病网络的新型系统方法。我们首先使用先前开发的网络拓扑算法(NeTA)在人类蛋白质相互作用数据中识别拓扑模块。然后使用基因本体论将所得模块与功能术语相关联,以获得功能模块。最后,通过将这些模块与OMIM和全基因组关联研究(GWAS)相关联来构建疾病模块。我们发现大多数拓扑模块具有凝聚结构、显著的通路注释和良好的模块性。大多数功能模块(70.6%)完全覆盖相应的拓扑模块,并且大多数疾病模块(88.5%)被相应的功能模块完全覆盖。此外,我们鉴定了几个感兴趣的蛋白质模块并进行了详细描述,这证明了我们整合方法的强大功能。这种方法使我们能够将基因、通路与其相应的疾病联系起来,这最终可能有助于我们改善疾病的预防、诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bb4/4585831/96013c915f52/srep14344-f8.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bb4/4585831/96013c915f52/srep14344-f8.jpg
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