Abstract

BackgroundThe p53 signalling pathway has hundreds of inputs and outputs. It can trigger cellular senescence, cell-cycle arrest and apoptosis in response to diverse stress conditions, including DNA damage, hypoxia and nutrient deprivation. Signals from all these inputs are channeled through a single node, the transcription factor p53. Yet, the pathway is flexible enough to produce different downstream gene expression patterns in response to different stresses.ResultsWe construct a mathematical model of the negative feedback loop involving p53 and its inhibitor, Mdm2, at the core of this pathway, and use it to examine the effect of different stresses that trigger p53. In response to DNA damage, hypoxia, etc., the model exhibits a wide variety of specific output behaviour - steady states with low or high levels of p53 and Mdm2, as well as spiky oscillations with low or high average p53 levels.ConclusionsWe show that even a simple negative feedback loop is capable of exhibiting the kind of flexible stress-specific response observed in the p53 system. Further, our model provides a framework for predicting the differences in p53 response to different stresses and single nucleotide polymorphisms.

Highlights

  • The p53 signalling pathway has hundreds of inputs and outputs

  • Our model provides a framework for predicting the differences in p53 response to different stresses and single nucleotide polymorphisms

  • Hypoxia invariably leads to apoptosis [4], whereas ribonucleotide depletion leads to reversible cell cycle arrest [5], and UV irradiation can result in either cell cycle arrest or apoptosis depending on the intensity of the damage [6]

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Summary

Results

We construct a mathematical model of the negative feedback loop involving p53 and its inhibitor, Mdm, at the core of this pathway, and use it to examine the effect of different stresses that trigger p53. In response to DNA damage, hypoxia, etc., the model exhibits a wide variety of specific output behaviour - steady states with low or high levels of p53 and Mdm, as well as spiky oscillations with low or high average p53 levels

Conclusions
Background
Methods
Results and Discussion
15 DNA damage Hypoxia
10 Fold change in parameter
38. Gillespie DT
45. Pahl HL
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