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Updated: Aug 12, 2026

Examination of Mitotic and Meiotic Fission Yeast Nuclear Dynamics by Fluorescence Live-cell Microscopy
Published on: June 24, 2019
Control over the onset of DNA synthesis in fission yeast
1Cell Cycle Control Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, U.K.
Abstract:
The fission yeast Schizosaccharomyces pombe has been used to identify gene functions required for the cell to become committed to the mitotic cell cycle and to initiate the processes leading to chromosome replication in S-phase. Two gene functions cdc2 and cdc10 must be executed for the cell to traverse 'start' and proceed from G1 into S-phase. Before the completion of these two functions the cell is in an uncommitted state and can undergo alternative developmental fates such as conjugation. A third gene, suc1, has also been identified whose product may interact directly with that of cdc2 at 'start'. The molecular functions of the genes involved in the completion of 'start' have been investigated. The cdc2 gene has been shown to be a protein kinase, suggesting that phosphorylation may be involved in the control over the transition from G1 into S-phase. The biochemical functions of the cdc10 and suc1 gene products have not yet been elucidated. A control at 'start' has also been shown to exist in the budding yeast Saccharomyces cerevisiae. Traverse of 'start' requires the execution of the CDC28 gene function. The cdc2 and CDC28 gene products (lower-case letters represent genes of Schizosaccharomyces pombe, and capital letters genes of Saccharomyces cerevisiae) are functionally homologous, suggesting that the processes involved in traverse of 'start' are highly conserved. An analogous control may also exist in the G1 period of mammalian cells, suggesting that the 'start' control step, after which cells become committed to the mitotic cell cycle, may have been conserved through evolution.
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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