Network-Based Disease Module Discovery by a Novel Seed Connector Algorithm with Pathobiological Implications

JOURNAL OF MOLECULAR BIOLOGY

卷:430

Article

Wang, Rui-Sheng¹  Loscalzo, Joseph¹ 

[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA

关键词: disease module;    seed connector;    network algorithms;    pathobiology;   

DOI  :  10.1016/j.jmb.2018.05.016

来源: Elsevier

【 摘 要 】

Understanding the genetic basis of complex diseases is challenging. Prior work shows that disease-related proteins do not typically function in isolation. Rather, they often interact with each other to form a network module that underlies dysfunctional mechanistic pathways. Identifying such disease modules will provide insights into a systems-level understanding of molecular mechanisms of diseases. Owing to the incompleteness of our knowledge of disease proteins and limited information on the biological mediators of pathobiological processes, the key proteins (seed proteins) for many diseases appear scattered over the human protein-protein interactome and form a few small branches, rather than coherent network modules. In this paper, we develop a network-based algorithm, called the Seed Connector algorithm (SCA), to pinpoint disease modules by adding as few additional linking proteins (seed connectors) to the seed protein pool as possible. Such seed connectors are hidden disease module elements that are critical for interpreting the functional context of disease proteins. The SCA aims to connect seed disease proteins so that disease mechanisms and pathways can be decoded based on predicted coherent network modules. We validate the algorithm using a large corpus of 70 complex diseases and binding targets of over 200 drugs, and demonstrate the biological relevance of the seed connectors. Lastly, as a specific proof of concept, we apply the SCA to a set of seed proteins for coronary artery disease derived from a meta-analysis of large-scale genome-wide association studies and obtain a coronary artery disease module enriched with important disease-related signaling pathways and drug targets not previously recognized. (C) 2018 Elsevier Ltd. All rights reserved.

【 授权许可】

Free