Control over the onset of DNA synthesis in fission yeast

V Simanis1, J Hayles, P Nurse

  • 1Cell Cycle Control Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.

Insights

Fission yeast studies reveal that cdc2 and cdc10 gene functions are essential for cell cycle commitment and entry into S-phase. This

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Genetics

Background:

  • The fission yeast Schizosaccharomyces pombe is a model organism for studying cell cycle control.
  • Understanding the transition from G1 to S-phase is crucial for cell proliferation and development.

Purpose of the Study:

  • To identify and characterize gene functions regulating the G1/S-phase transition ('start') in S. pombe.
  • To investigate the molecular mechanisms underlying cell cycle commitment.

Main Methods:

  • Genetic analysis in Schizosaccharomyces pombe.
  • Biochemical characterization of gene products.
  • Comparative studies with budding yeast Saccharomyces cerevisiae.

Main Results:

  • Two essential gene functions, cdc2 and cdc10, are required for cells to traverse 'start' and enter S-phase.
  • The cdc2 gene product is a protein kinase, indicating a role for phosphorylation in G1/S-phase control.
  • The suc1 gene product may interact with cdc2 at 'start'.
  • Functional homology between S. pombe cdc2 and S. cerevisiae CDC28 suggests conserved 'start' control mechanisms.

Conclusions:

  • The 'start' transition in S. pombe is a critical control point for cell cycle commitment.
  • Phosphorylation is likely involved in regulating the G1 to S-phase progression.
  • The 'start' control mechanism appears to be evolutionarily conserved across yeast species and potentially in mammalian cells.

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