Modeling the Control of Meiotic Cell Divisions: Entry, Progression, and Exit

Biophys J. 2020 Sep 1;119(5):1015-1024. doi: 10.1016/j.bpj.2020.07.017. Epub 2020 Jul 29.

Abstract

Upon nitrogen starvation, Schizosaccharomyces pombe exit the mitotic cell cycle and become irreversibly committed to the completion of meiosis program. Meiotic cell divisions are coordinated with sporulation events to produce haploid spores. In the last few decades, experiments on fission yeast have revealed different molecular players involved in two meiotic cell divisions, meiosis I (MI) and meiosis II (MII). How the MI entry, MI-to-MII transition, and MII exit occur because of the dynamics of the regulatory network is not well understood. In this work, we developed a comprehensive mathematical model of the network that describes the temporal dynamics of meiotic progression. The model accounts for the phenotypes of several experimental data (single and multiple mutations). We demonstrate the control strategy involving multiple feedback loops to yield two successive division cycles. The differential regulation of anaphase-promoting complex/cyclosome (APC/C) coactivators and its inhibitors is crucial for the dynamics of both MI-to-MII transition and MII exit. This model generates mechanistic insights that help in further experiments and modeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase-Promoting Complex-Cyclosome
  • Cell Cycle Proteins / genetics
  • Meiosis
  • Phenotype
  • Schizosaccharomyces pombe Proteins* / genetics
  • Schizosaccharomyces*

Substances

  • Cell Cycle Proteins
  • Schizosaccharomyces pombe Proteins
  • Anaphase-Promoting Complex-Cyclosome