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iTraNet: a web-based platform for integrated trans-omics network visualization and analysis
Hikaru Sugimoto1, Keigo Morita2,3, Dongzi Li2
1Department of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.
iTraNet visualizes and analyzes trans-omics networks, integrating gene regulatory, protein-protein interaction, and metabolic data. This tool revealed differences in molecular responses to glucose between wild-type and obese mice.
Area of Science:
- Systems biology
- Bioinformatics
- Computational biology
Background:
- Understanding biological systems relies on analyzing diverse molecular networks, including gene regulatory, protein-protein interaction, and metabolic networks.
- Analyzing these networks is complex due to varied databases and intricate analysis methods.
- Metabolic networks involve substrates, products, and enzymes, influenced by allosteric regulation and gene expression.
Purpose of the Study:
- To develop a web application, iTraNet, for visualizing and analyzing integrated trans-omics networks.
- To investigate differences in molecular responses to glucose administration in wild-type versus obese (ob/ob) mice using network analysis.
Main Methods:
- Development of iTraNet, a web application integrating gene regulatory, protein-protein interaction, metabolic, and metabolite exchange networks.
- Application of iTraNet to analyze trans-omics data from wild-type and ob/ob mice.
- Comparative analysis of network hub molecule responses to glucose administration.
Main Results:
- iTraNet successfully visualizes and analyzes integrated trans-omics networks.
- In wild-type mice, key network molecules responded to glucose administration.
- This response pattern was absent in ob/ob mice, indicating altered metabolic regulation.
Conclusions:
- iTraNet provides a valuable tool for researchers to explore complex biological networks.
- Network analysis using iTraNet can revealSystemic differences in physiological responses, such as those related to obesity and glucose metabolism.
- The findings highlight potential disruptions in molecular signaling pathways in obesity.
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