期刊
IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS
卷 18, 期 6, 页码 2239-2248出版社
IEEE COMPUTER SOC
DOI: 10.1109/TCBB.2020.2970400
关键词
Optimization; Nonhomogeneous media; Gene expression; Heuristic algorithms; Proteins; Immune system; Active modules; gene co-expression networks; continuous optimization; Th17 cell differentiation
类别
资金
- Royal Society [BIR002]
- EU FP7 [FP7-NMP-2012-LARGE-6]
Identifying active modules in biological networks is crucial for understanding regulatory and signaling mechanisms. Existing methods rely on protein-protein interaction or metabolic networks, while the newly proposed AMOUNTAIN algorithm utilizes weighted gene co-expression networks to identify active modules, even in cross-species and dynamic contexts.
Searching for active modules, i.e., regions showing striking changes in molecular activity in biological networks is important to reveal regulatory and signaling mechanisms of biological systems. Most existing active modules identification methods are based on protein-protein interaction networks or metabolic networks, which require comprehensive and accurate prior knowledge. On the other hand, weighted gene co-expression networks (WGCNs) are purely constructed from gene expression profiles. However, existing WGCN analysis methods are designed for identifying functional modules but not capable of identifying active modules. There is an urgent need to develop an active module identification algorithm for WGCNs to discover regulatory and signaling mechanism associating with a given cellular response. To address this urgent need, we propose a novel algorithm called active modules on the multi-layer weighted (co-expression gene) network, based on a continuous optimization approach (AMOUNTAIN). The algorithm is capable of identifying active modules not only from single-layer WGCNs but also from multilayer WGCNs such as cross-species and dynamic WGCNs. We first validate AMOUNTAIN on a synthetic benchmark dataset. We then apply AMOUNTAIN to WGCNs constructed from Th17 differentiation gene expression datasets of human and mouse, which include a single layer, a cross-species two-layer and a multilayer dynamic WGCNs. The identified active modules from WGCNs are enriched by known protein-protein interactions, and more importantly, they reveal some interesting and important regulatory and signaling mechanisms of Th17 cell differentiation.
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