Estimating gene regulatory networks and proteinprotein interactions of Saccharomyces cerevisiae from multiple genome-wide data
1Human Genome Center, Institute of Medical Science, University of Tokyo 4-6-1 Shirokanedai, Minato-ku, Tokyo, 108-8639, Japan
2Bioinformatics Center, Institute for Chemical Research, Kyoto University Gokasho, Uji, Kyoto, 611-0011, Japan
*To whom correspondence should be addressed.
Motivation: Biological processes in cells are properly performed by gene regulations, signal transductions and interactions between proteins. To understand such molecular networks, we propose a statistical method to estimate gene regulatory networks and proteinprotein interaction networks simultaneously from DNA microarray data, proteinprotein interaction data and other genome-wide data.
Results: We unify Bayesian networks and Markov networks for estimating gene regulatory networks and proteinprotein interaction networks according to the reliability of each biological information source. Through the simultaneous construction of gene regulatory networks and proteinprotein interaction networks of Saccharomyces cerevisiae cell cycle, we predict the role of several genes whose functions are currently unknown. By using our probabilistic model, we can detect false positives of high-throughput data, such as yeast two-hybrid data. In a genome-wide experiment, we find possible gene regulatory relationships and proteinprotein interactions between large protein complexes that underlie complex regulatory mechanisms of biological processes.
Contact: nariai{at}ims.u-tokyo.ac.jp
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