Integrated analysis of regulatory and metabolic networks reveals novel regulatory mechanisms in Saccharomyces cerevisiae

  1. Markus J. Herrgård,
  2. Baek-Seok Lee1,
  3. Vasiliy Portnoy, and
  4. Bernhard Ø. Palsson2
  1. Department of Bioengineering, University of California, San Diego, La Jolla, California 92093-0412, USA
  1. 1

    1 Present address: Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0017, Japan.

Abstract

We describe the use of model-driven analysis of multiple data types relevant to transcriptional regulation of metabolism to discover novel regulatory mechanisms in Saccharomyces cerevisiae. We have reconstructed the nutrient-controlled transcriptional regulatory network controlling metabolism in S. cerevisiae consisting of 55 transcription factors regulating 750 metabolic genes, based on information in the primary literature. This reconstructed regulatory network coupled with an existing genome-scale metabolic network model allows in silico prediction of growth phenotypes of regulatory gene deletions as well as gene expression profiles. We compared model predictions of gene expression changes in response to genetic and environmental perturbations to experimental data to identify potential novel targets for transcription factors. We then identified regulatory cascades connecting transcription factors to the potential targets through a systematic model expansion strategy using published genome-wide chromatin immunoprecipitation and binding-site-motif data sets. Finally, we show the ability of an integrated metabolic and regulatory network model to predict growth phenotypes of transcription factor knockout strains. These studies illustrate the potential of model-driven data integration to systematically discover novel components and interactions in regulatory and metabolic networks in eukaryotic cells.

Footnotes

  • 2

    2 Corresponding author.

    2 E-mail palsson{at}ucsd.edu; fax (858) 822-3120.

  • [Supplemental material is available online at www.genome.org.]

  • Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.4083206

  • 3

    3 See Reed et al. (2003) for conventions used for naming in silico strains. MH refers to the principal person responsible for reconstructing the model, 805 is the number of genes accounted for by the model, and 775 is the number of regulatory interactions in the model.

    • Received April 30, 2005.
    • Accepted February 23, 2006.
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