NetDecoder: a network biology platform that decodes context-specific biological networks and gene activities

被引:22
作者
da Rocha, Edroaldo Lummertz [1 ]
Ung, Choong Yong [1 ]
McGehee, Cordelia D. [1 ]
Correia, Cristina [1 ]
Li, Hu [1 ]
机构
[1] Mayo Clin, Coll Med, Ctr Individualized Med, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
UNFOLDED PROTEIN RESPONSE; BREAST-CANCER; EDGETIC PERTURBATION; MEMORY FORMATION; EXPRESSION; CELL; PLEIOTROPY; INHIBITOR; SURVIVAL; NODES;
D O I
10.1093/nar/gkw166
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sequential chain of interactions altering the binary state of a biomolecule represents the 'information flow' within a cellular network that determines phenotypic properties. Given the lack of computational tools to dissect context-dependent networks and gene activities, we developed NetDecoder, a network biology platform that models context-dependent information flows using pairwise phenotypic comparative analyses of protein-protein interactions. Using breast cancer, dyslipidemia and Alzheimer's disease as case studies, we demonstrate NetDecoder dissects subnetworks to identify key players significantly impacting cell behaviour specific to a given disease context. We further show genes residing in disease-specific subnetworks are enriched in disease-related signalling pathways and information flow profiles, which drive the resulting disease phenotypes. We also devise a novel scoring scheme to quantify key genes-network routers, which influence many genes, key targets, which are influenced by many genes, and high impact genes, which experience a significant change in regulation. We show the robustness of our results against parameter changes. Our network biology platform includes freely available source code (http://www.NetDecoder.org) for researchers to explore genome-wide context-dependent information flow profiles and key genes, given a set of genes of particular interest and transcriptome data. More importantly, NetDecoder will enable researchers to uncover context-dependent drug targets.
引用
收藏
页数:13
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