Modeling the START transition in the budding yeast cell cycle
Abstract
Budding yeast, Saccharomyces cerevisiae, is widely used as a model organism to study the genetics underlying eukaryotic cellular processes and growth critical to cancer development, such as cell division and cell cycle progression. The budding yeast cell cycle is also one of the best-studied dynamical systems owing to its thoroughly resolved genetics. However, the dynamics underlying the crucial cell cycle decision point called the START transition, at which the cell commits to a new round of DNA replication and cell division, are under-studied. The START machinery involves a central cyclin-dependent kinase; cyclins responsible for starting the transition, bud formation, and initiating DNA synthesis; and their transcriptional regulators. However, evidence has shown that the mechanism is more complicated than a simple irreversible transition switch. Activating a key transcription regulator SBF requires the phosphorylation of its inhibitor, Whi5, or an SBF/MBF monomeric component, Swi6, but not necessarily both. Also, the timing and mechanism of the inhibitor Whi5s nuclear export, while important, are not critical for the timing and execution of START. Therefore, there is a need for a consolidated model for the budding yeast START transition, reconciling all known regulatory and spatial dynamics. We built a detailed mathematical model (START-BYCC) for the START transition in the budding yeast cell cycle based on all established molecular interactions and experimental phenotypes. START-BYCC recapitulates the underlying dynamics and correctly emulates key phenotypic traits of [~]150 known START mutants, including regulation of size control, localization of inhibitor/transcription factor complexes, and the nutritional effects on size control. Such a detailed mechanistic understanding of the underlying dynamics gets us closer towards deconvoluting the aberrant cellular development in cancer. All wildtype and mutant simulations of our START-BYCC model are available at sbmlsimulator.org/simulator/by-start, and the supporting data is available on GitHub: github.com/jravilab/start-bycc.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 2
- FWCI
- 0.27
- Field percentile
- 46th percentile
- Organism
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Normal and Aberrant Cell Cycles Characterized by a Continuous-Time Stochastic Boolean Model of Cell Cycle Regulation in Budding Yeast
Kittisak Taoma, John J. Tyson, … Pavel Kraikivski·bioRxiv·Jan 4, 2024
- Cell Size Modulates SBF and Whi5 Chromatin Binding to Regulate the Start of the Budding Yeast Cell Cycle
Huan Zheng, Ana Paulina Gutierrez Alejandre, … Rodrigo Reyes‐Lamothe·bioRxiv·Feb 17, 2026
- Dilution and titration of cell-cycle regulators may control cell size in budding yeast
Frank S. Heldt, Reece Lunstone, … Béla Novák·PLoS Computational BiologyPeer-reviewed·Oct 24, 2018
- When Yeast Cells Change their Mind: Cell Cycle 'Start' is Reversible under Starvation
D. Irvali, F. P. Schlottmann, … J. C. Ewald·bioRxiv·Oct 31, 2021
- A Hybrid Stochastic Model of the Budding Yeast Cell Cycle
Mansooreh Ahmadian, John J. Tyson, … Yang Cao·npj Systems Biology and ApplicationsPeer-reviewed·Mar 27, 2020
- Whi5 hypo- and hyper- phosphorylation dynamics control cell cycle entry and progression
J. Y. Xiao, J. J. Turner, … J. Skotheim·bioRxiv·Nov 2, 2023