A dynamic P53-MDM2 model with time delay
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Abstract: Specific activator and repressor transcription factors which bind to specific regulator DNA sequences, play an important role in gene activity control. Interactions between genes coding such transcription factors should explain the different stable or sometimes oscillatory gene activities characteristic for different tissues. Starting with the model P53-MDM2 described into [6] and the process described into [5] we developed a new model of this interaction. Choosing the delay as a bifurcation parameter we study the direction and stability of the bifurcating periodic solutions. Some numerical examples are finally given for justifying the theoretical results.
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Cites work
Cited in
(12)- A simple model of genetic oscillations through regulated degradation
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- Influence of the nuclear membrane, active transport, and cell shape on the Hes1 and p53-Mdm2 pathways: insights from spatio-temporal modelling
- Mathematical analysis of a generalised p53-Mdm2 protein gene expression model
- Analysis of a minimal model for p53 oscillations
- The dynamics of genetic control in the cell: the good and bad of being late
- HOPF BIFURCATION ANALYSIS FOR A MATHEMATICAL MODEL OF P53-MDM2 INTERACTION
- Spatio-Temporal Modelling of the p53–mdm2 Oscillatory System
- P53-Mdm2 Loop Stability and Oscillatory Dynamics with Mdm2-Induced Delay Effect in P53
- Pattern Formation and Oscillations in Reaction–Diffusion Model with p53-Mdm2 Feedback Loop
- Oscillatory expression and variability in p53 regulatory network
- Stability and bifurcation analysis of a simple delayed p53-Mdm2 gene network model with diffusion
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