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A protein-protein interaction (PPI) network in the liver of offspring rats exposed to maternal hypoxia was investigated using proteome-derived data. In this study, we assessed the maternal hypoxia-induced changes in proteins implicated in the PPI network by protein-protein interaction analysis (PRINET) with the transcriptome of livers from offspring rats. By applying two different methods, PRINET analysis based on the predicted interaction and PRINET analysis based on the experimentally validated interaction in the Gene Ontology database, we identified 30 different proteins that were upregulated and 34 proteins that were downregulated in the offspring liver after exposure to maternal hypoxia. The PPI network of selected upregulated proteins has been reconstructed, and the network structure of upregulated proteins was analyzed. GO and pathway analyses in the reconstructed network showed that the altered protein sets were involved in a variety of biological processes, including cellular metabolic and regulatory processes, protein transportation, cell differentiation, signal transduction, and apoptosis. Moreover, we identified a number of differentially expressed proteins that have been reported to be implicated in the PPI network. These results support the usefulness of integrated proteome analysis for constructing a comprehensive PPI network of fetal proteins that could be a promising approach for understanding the complexity of fetal proteome.Q:
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