Article

Zhu, J. et al. Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks. Nat. Genet. 40, 854-861

Rosetta Inpharmatics, LLC, Seattle, Washington 98109, USA.
Nature Genetics (Impact Factor: 29.35). 08/2008; 40(7):854-61. DOI: 10.1038/ng.167
Source: PubMed

ABSTRACT

A key goal of biology is to construct networks that predict complex system behavior. We combine multiple types of molecular data, including genotypic, expression, transcription factor binding site (TFBS), and protein-protein interaction (PPI) data previously generated from a number of yeast experiments, in order to reconstruct causal gene networks. Networks based on different types of data are compared using metrics devised to assess the predictive power of a network. We show that a network reconstructed by integrating genotypic, TFBS and PPI data is the most predictive. This network is used to predict causal regulators responsible for hot spots of gene expression activity in a segregating yeast population. We also show that the network can elucidate the mechanisms by which causal regulators give rise to larger-scale changes in gene expression activity. We then prospectively validate predictions, providing direct experimental evidence that predictive networks can be constructed by integrating multiple, appropriate data types.

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Available from: Roger Bumgarner, Feb 19, 2014
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    • "For example, gene co-expression networks constructed with correlation-based measures have been used to identify transitive relationships (Zhou et al., 2002), gene regulatory patterns (van Noort et al., 2004), and biological modules (Mason et al., 2009). Further, they have been successfully combined with transcription factor, eQTL, and PPI data into integrative Bayesian networks (Zhu et al., 2008). Gene co-expression networks are therefore one commonly used example of a complex model built from the high-throughput biological data collections. "
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