modelcell

cell

Extends from BioChem.Compartments.MainCompartment (Main compartment (constant volume)).

Information

A Simple Mitotic Oscillator

This example is a modelica version of the model presented in A minimal cascade model for the miotic oscillator involving cyclin and cdc2 kinase by Goldbeter A. (Proc. Nati. Acad. Sci. USA Vol. 88, pp. 9107-9111, October 1991 Cell Biology.)

Abstract

A minimal model for the mitotic oscillator is presented. The model, built on recent experimental advances, is based on the cascade of post-translational modification that modulates the activity of cdc2 kinase during the cell cycle. The model pertains to the situation encountered in early amphibian embryos, where the accumulation of cyclin suffices to trigger the onset of mitosis. In the first cycle of the bicyclic cascade model, cyclin promotes the activation of cdc2 kinase through reversible dephosphorylation, and in the second cycle, cdc2 kinase activates a cyclin protease by reversible phosphorylation. That cyclin activates cdc2 kinase while the kinase triggers the degradation of cyclin has suggested that oscillations may originate from such a negative feedback loop [Félix, M. A., Labbé, J. C., Dorée, M., Hunt, T. & Karsenti, E. (1990) Nature (London) 346, 379-382]. This conjecture is corroborated by the model, which indicates that sustained oscillations of the limit cycle type can arise in the cascade, provided that a threshold exists in the activation of cdc2 kinase by cyclin and in the activation of cyclin proteolysis by cdc2 kinase. The analysis shows how miototic oscillations may readily arise from time lags associated with these thresholds and from the delayed negative feedback provided by cdc2-induced cyclin degradation. A mechanism for the origin of the thresholds is proposed in terms of the phenomenon of zero-order ultrasensitivity previously described for biochemical systems regulated by covalent modification.

Simulations

The simulation results are shown in the Figure 1. This plot corresponds to Fig 3 of the paper (Goldbeter 1991). Fig1: Simulation results

Parameters

TypeNameDefaultDescription
RealVM13VM1
RealVM31VM3
RealKc0.5Kc

Components

TypeNameDefaultDescription
BioChem.Units.VolumeV (from Compartment)Compartment volume
Realcell_VVVariable used to make the compartment volume accessible for inner components. Do not edit.
BioChem.Examples.GMO.cell.C_CCyclin
BioChem.Examples.GMO.cell.M_MCDC-2 Kinase
BioChem.Examples.GMO.cell.X_XCyclin Protease
RealV1V1
RealV3V3
BioChem.Substances.AmbientSubstanceambientSubstance
BioChem.Examples.GMO.cell.reaction1_reaction1creation of cyclin
BioChem.Examples.GMO.cell.reaction2_reaction2default degradation of cyclin
BioChem.Examples.GMO.cell.reaction3_reaction3cdc2 kinase triggered degration of cyclin
BioChem.Examples.GMO.cell.reaction4_reaction4activation of cdc2 kinase
BioChem.Examples.GMO.cell.reaction5_reaction5deactivation of cdc2 kinase
BioChem.Examples.GMO.cell.reaction6_reaction6activation of cyclin protease
BioChem.Examples.GMO.cell.reaction7_reaction7deactivation of cyclin protease

Contents

NameDescription
C_
M_
X_
reaction1_
reaction2_
reaction3_
reaction4_
reaction5_
reaction6_
reaction7_