The cycle of cell growth, DNA synthesis, mitosis and cell division is the fundamental process by which cells (and all living organisms) grow, develop and reproduce. Hence, it is of crucial importance to science and human health to understand the molecular mechanisms that control these processes in eukaryotic cells. The control system is so complex that mathematical and computational methods are needed to reliably track the interactions of all the relevant genes, mRNAs, proteins, and multiprotein complexes. Deterministic models (ordinary differential equations) are adequate for understanding the average behavior of groups of cells, but to understand the far-from-average behavior of individual cells requires stochastic models that accurately account for noise stemming from small numbers of participating molecules within a single cell and from vagaries of the division process (i.e., unequal partitioning of molecular components between daughter cells). Accurately modeling the variable responses among cells in a population may be critical to understanding abnormal and diseased cell proliferation. The goals of the proposed renewal are to 1) develop a realistic and accurate stochastic model of cell cycle control in budding yeast and to extend this model to the control of mammalian cell proliferation, 2) measure stochastic effects in single yeast cells in order to provide experimental constraints on and tests of the model, and 3) develop effective algorithms and software to support stochastic modeling and simulation, and to make these tools readily available to the scientific community. Our multi-disciplinary team at Virginia Tech has proven expertise in all aspects of the project and close collaborations with top researchers in the areas of stochastic simulation, sensitivity analysis, bifurcation theory, modeling software, and yeast genetics. Because all eukaryotic cells seem to employ the same fundamental molecular machinery that regulates the cell cycle of yeast, success in modeling growth and division of single yeast cells will translate into better understanding of the role of mammalian cell division in basic biological processes of significance to human health: e.g., embyronic development, tissue regeneration, wound healing, and carcinogenesis.

Public Health Relevance

The cell division cycle is the fundamental process of biological growth and reproduction, and mistakes in this process underlie many serious health problems, especially cancer. An integrative understanding of the cellular basis of health and disease will require, among other things, a description of the cell cycle by computational models that account accurately for the reliability of DNA replication and inheritance despite the molecular fluctuations that inevitably occur in the small confines of a living cell. Hence, a validated stochastic model of the eukaryotic cell cycle is essential to progress in the field of molecular systems biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM078989-08
Application #
8536829
Study Section
Modeling and Analysis of Biological Systems Study Section (MABS)
Program Officer
Lyster, Peter
Project Start
2006-06-06
Project End
2014-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
8
Fiscal Year
2013
Total Cost
$466,851
Indirect Cost
$164,897
Name
Virginia Polytechnic Institute and State University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
003137015
City
Blacksburg
State
VA
Country
United States
Zip Code
24061
Novák, Béla; Heldt, Frank Stefan; Tyson, John J (2018) Genome Stability during Cell Proliferation: A Systems Analysis of the Molecular Mechanisms Controlling Progression through the Eukaryotic Cell Cycle. Curr Opin Syst Biol 9:22-31
Hopkins, Michael; Tyson, John J; Novák, Béla (2017) Cell-cycle transitions: a common role for stoichiometric inhibitors. Mol Biol Cell 28:3437-3446
Oguz, Cihan; Watson, Layne T; Baumann, William T et al. (2017) Predicting network modules of cell cycle regulators using relative protein abundance statistics. BMC Syst Biol 11:30
Laomettachit, Teeraphan; Chen, Katherine C; Baumann, William T et al. (2016) A Model of Yeast Cell-Cycle Regulation Based on a Standard Component Modeling Strategy for Protein Regulatory Networks. PLoS One 11:e0153738
Barik, Debashis; Ball, David A; Peccoud, Jean et al. (2016) A Stochastic Model of the Yeast Cell Cycle Reveals Roles for Feedback Regulation in Limiting Cellular Variability. PLoS Comput Biol 12:e1005230
Palmisano, Alida; Hoops, Stefan; Watson, Layne T et al. (2015) JigCell Run Manager (JC-RM): a tool for managing large sets of biochemical model parametrizations. BMC Syst Biol 9:95
Wang, Shuo; Cao, Yang (2015) The Abridgment and Relaxation Time for a Linear Multi-Scale Model Based on Multiple Site Phosphorylation. PLoS One 10:e0133295
Gérard, Claude; Tyson, John J; Coudreuse, Damien et al. (2015) Cell cycle control by a minimal Cdk network. PLoS Comput Biol 11:e1004056
Tyson, John J; Novak, Bela (2015) Bistability, oscillations, and traveling waves in frog egg extracts. Bull Math Biol 77:796-816
Hong, Tian; Oguz, Cihan; Tyson, John J (2015) A Mathematical Framework for Understanding Four-Dimensional Heterogeneous Differentiation of CD4+ T Cells. Bull Math Biol 77:1046-64

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