Complex transcriptional circuitry at the G1/S transition in Saccharomyces cerevisiae

  1. Christine E. Horak1,
  2. Nicholas M. Luscombe2,
  3. Jiang Qian2,
  4. Paul Bertone1,
  5. Stacy Piccirrillo1,
  6. Mark Gerstein2, and
  7. Michael Snyder1,3
  1. 1Department of Molecular, Cellular, and Developmental Biology and 2Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8103, USA

Abstract

In the yeast Saccharomyces cerevisiae, SBF (Swi4–Swi6 cell cycle box bindingfactor) and MBF ( M luIbinding factor) are the major transcription factors regulating the START of the cell cycle, a time just before DNA replication, bud growth initiation, and spindle pole body (SPB) duplication. These two factors bind to the promoters of 235 genes, but bind less than a quarter of the promoters upstream of genes with peak transcript levels at the G1 phase of the cell cycle. Several functional categories, which are known to be crucial for G1/S events, such as SPB duplication/migration and DNA synthesis, are under-represented in the list of SBF and MBF gene targets. SBF binds the promoters of several other transcription factors, includingHCM1, PLM2, POG1, TOS4, TOS8,TYE7, YAP5, YHP1, and YOX1. Here, we demonstrate that these factors are targets of SBF using an independent assay. To further elucidate the transcriptional circuitry that regulates the G1-to-S-phase progression, these factors were epitope-tagged and their binding targets were identified by chIp–chip analysis. These factors bind the promoters of genes with roles in G1/S events including DNA replication, bud growth, and spindle pole complex formation, as well as the general activities of mitochondrial function, transcription, and protein synthesis. Although functional overlap exists between these factors and MBF and SBF, each of these factors has distinct functional roles. Most of these factors bind the promoters of other transcription factors known to be cell cycle regulated or known to be important for cell cycle progression and differentiation processes indicating that a complex network of transcription factors coordinates the diverse activities that initiate a new cell cycle.

Keywords

Footnotes

  • 3 Corresponding author.

  • EMAIL michael.snyder{at}yale.edu; FAX (203) 432-6161.

  • Supplemental material is available at http://www.genesdev.org.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1039602.

    • Received September 9, 2002.
    • Accepted October 9, 2002.
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