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Chapter category: Gene Expression

Elucidating Gene Regulatory Networks Underlying Complex Phenotypes: Genetical Genomics and Bayesian Network

This chapter appears in the following book:

Microarrays and Transcription Networks

Edited by: M. Frances Shannon and Sudha Rao
ISBN: 1-58706-290-9
» Get more information about this book at landesbioscience.com «

Chapter authors:
Yan Cui


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Microarray-based technologies have enabled comprehensive transcriptome profiling. It is becoming feasible to reconstruct gene transcriptional regulatory networks from microarray data. In this chapter, I outline a new strategy for reconstructing gene regulatory networks as part of the causal network through which genetic variations influence phenotypes. A central step of phenotype manifestation is gene transcription. The gene expression programs encoded in DNA sequences are executed via the network of transcriptional regulation. Thus, the gene regulatory networks can be studied as the causal pathways connecting genetic loci and phenotypes. Bayesian network modeling combined with genetical genomics methods provides a promising method for inferring the causal network from multiple types of data. The complete causal network should include nodes (variables) representing genetic variations (e.g., single nucleotide polymorphisms); environmental factors (experimental conditions); phenotypes; and abundances of RNAs, proteins and other bio-molecules. Currently, the reconstruction of the causal network focuses on the interactions between genetic variations, abundance of mRNAs, and phenotypes because large-scale data are available for these components. Advances in molecular profiling will eventually provide sufficient data for all the bio-molecules and thus enable the reconstruction of the complete causal network underlying complex phenotypes. This causal network is important not only for understanding the structure of gene regulatory network, but also because it provides deep insights into the molecular underpinnings of genotype-environment-phenotype relations, which are invaluable for uncovering the genetic basis of diseases and predicting the outcomes of therapeutic interventions.

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