G1/S transition and cell population dynamics
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1.
Institut de Recherche pour le Développement, 32 avenue Henri Varagnat 93143 Bondy Cedex
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2.
Laboratory of Cancer Pharmacogenomics, Fondo Edo Tempia, via Malta 3, 13900 Biella
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3.
Iowa State University, Department of Mathematics, 482 Carver Hall Ames, IA 50011
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Received:
01 February 2008
Revised:
01 November 2008
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92D25, 92C40, 58K55.
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In this paper we present a model connecting the state of molecular components during the cell cycle at the individual level to the population dynamic. The complexes Cyclin E/CDK2 are good markers of the cell state in its cycle. In this paper we focus on the first transition phase of the cell cycle ($S-G_{2}-M$) where the complexe Cyclin E/CDK2 has a key role in this transition. We give a simple system of differential equations to represent the dynamic of the Cyclin E/CDK2 amount during the cell cycle, and couple it with a cell population dynamic in such way our cell population model is structured by cell age and the amount of Cyclin E/CDK2 with two compartments: cells in the G1 phase and cells in the remainder of the cell cycle ($S-G_{2}-M$). A cell transits from the G1 phase to the S phase when
Cyclin E/CDK2 reaches a threshold, which allow us to take into
account the variability in the timing of G1/S transition. Then the
cell passes through $S-G_{2}-M$ phases and divides with the
assumption of unequal division among daughter cells of the final
Cyclin E/CDK2 amount. The existence and the asymptotic behavior of the
solution of the model is analyzed.
Citation: Fadia Bekkal-Brikci, Giovanna Chiorino, Khalid Boushaba. G1/S transition and cell population dynamics[J]. Networks and Heterogeneous Media, 2009, 4(1): 67-90. doi: 10.3934/nhm.2009.4.67
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Abstract
In this paper we present a model connecting the state of molecular components during the cell cycle at the individual level to the population dynamic. The complexes Cyclin E/CDK2 are good markers of the cell state in its cycle. In this paper we focus on the first transition phase of the cell cycle ($S-G_{2}-M$) where the complexe Cyclin E/CDK2 has a key role in this transition. We give a simple system of differential equations to represent the dynamic of the Cyclin E/CDK2 amount during the cell cycle, and couple it with a cell population dynamic in such way our cell population model is structured by cell age and the amount of Cyclin E/CDK2 with two compartments: cells in the G1 phase and cells in the remainder of the cell cycle ($S-G_{2}-M$). A cell transits from the G1 phase to the S phase when
Cyclin E/CDK2 reaches a threshold, which allow us to take into
account the variability in the timing of G1/S transition. Then the
cell passes through $S-G_{2}-M$ phases and divides with the
assumption of unequal division among daughter cells of the final
Cyclin E/CDK2 amount. The existence and the asymptotic behavior of the
solution of the model is analyzed.
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