Steady States and Oscillations in the p53/Mdm2 Network

p53 is activated in response to events compromising the genetic integrity of a cell. Recent data show that p53 activity does not increase steadily with genetic damage but rather fluctuates in an oscillatory fashion (Lahav et al., Nature Genetics, 36, 147-150, 2004). Theoretical studies suggest that...

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Veröffentlicht in:Cell cycle (Georgetown, Tex.) Tex.), 2005-03, Vol.4 (3), p.488-493
Hauptverfasser: Ciliberto, Andrea, Novak, Bela, Tyson, John J.
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creator Ciliberto, Andrea
Novak, Bela
Tyson, John J.
description p53 is activated in response to events compromising the genetic integrity of a cell. Recent data show that p53 activity does not increase steadily with genetic damage but rather fluctuates in an oscillatory fashion (Lahav et al., Nature Genetics, 36, 147-150, 2004). Theoretical studies suggest that oscillations can arise from a combination of positive and negative feedbacks or from a long negative feedback loop alone. Both negative and positive feedbacks are present in the p53/Mdm2 network, but it is not known what roles they play in the oscillatory response to DNA damage. We developed a mathematical model of p53 oscillations based on positive and negative feedbacks in the p53/Mdm2 network. According to the model, the system reacts to DNA damage by moving from a stable steady state into a region of stable limit cycles. Oscillations in the model are born with large amplitude, which guarantees an all-or-none response to damage. As p53 oscillates, damage is repaired and the system moves back to a stable steady state with low p53 activity. The model reproduces experimental data in quantitative detail. We suggest new experiments for dissecting the contributions of negative and positive feedbacks to the generation of oscillations.
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Animals
Binding
Biology
Bioscience
Calcium
Cancer
Cell
Cell Cycle
Cycle
DNA Damage
Feedback, Physiological
Gene Expression Regulation
Humans
Landes
Models, Biological
Open Reading Frames
Organogenesis
Oscillometry
Proteins
Proto-Oncogene Proteins - chemistry
Proto-Oncogene Proteins c-mdm2 - chemistry
Proto-Oncogene Proteins c-mdm2 - metabolism
Transcription, Genetic
Tumor Suppressor Protein p53 - chemistry
Tumor Suppressor Protein p53 - metabolism
title Steady States and Oscillations in the p53/Mdm2 Network
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