Literature DB >> 15725723

Steady states and oscillations in the p53/Mdm2 network.

Andrea Ciliberto1, Béla Novak, John J Tyson.   

Abstract

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. 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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Year:  2005        PMID: 15725723     DOI: 10.4161/cc.4.3.1548

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  70 in total

1.  Coordination between cell cycle progression and cell fate decision by the p53 and E2F1 pathways in response to DNA damage.

Authors:  Xiao-Peng Zhang; Feng Liu; Wei Wang
Journal:  J Biol Chem       Date:  2010-08-04       Impact factor: 5.157

2.  Glucose oscillations, more than constant high glucose, induce p53 activation and a metabolic memory in human endothelial cells.

Authors:  B Schisano; G Tripathi; K McGee; P G McTernan; A Ceriello
Journal:  Diabetologia       Date:  2011-02-02       Impact factor: 10.122

Review 3.  The p53-MDM2 network: from oscillations to apoptosis.

Authors:  Indrani Bose; Bhaswar Ghosh
Journal:  J Biosci       Date:  2007-08       Impact factor: 1.826

4.  Rapid cycling and precocious termination of G1 phase in cells expressing CDK1AF.

Authors:  Joseph R Pomerening; Jeffrey A Ubersax; James E Ferrell
Journal:  Mol Biol Cell       Date:  2008-05-14       Impact factor: 4.138

5.  Recurrent initiation: a mechanism for triggering p53 pulses in response to DNA damage.

Authors:  Eric Batchelor; Caroline S Mock; Irun Bhan; Alexander Loewer; Galit Lahav
Journal:  Mol Cell       Date:  2008-05-09       Impact factor: 17.970

6.  Harmonic oscillations in homeostatic controllers: Dynamics of the p53 regulatory system.

Authors:  Ingunn W Jolma; Xiao Yu Ni; Ludger Rensing; Peter Ruoff
Journal:  Biophys J       Date:  2010-03-03       Impact factor: 4.033

Review 7.  Functional motifs in biochemical reaction networks.

Authors:  John J Tyson; Béla Novák
Journal:  Annu Rev Phys Chem       Date:  2010       Impact factor: 12.703

8.  Predicted functions of MdmX in fine-tuning the response of p53 to DNA damage.

Authors:  Sohyoung Kim; Mirit I Aladjem; Geoffrey B McFadden; Kurt W Kohn
Journal:  PLoS Comput Biol       Date:  2010-02-05       Impact factor: 4.475

9.  Analysis and verification of the HMGB1 signaling pathway.

Authors:  Haijun Gong; Paolo Zuliani; Anvesh Komuravelli; James R Faeder; Edmund M Clarke
Journal:  BMC Bioinformatics       Date:  2010-10-15       Impact factor: 3.169

10.  Modeling the role of p53 pulses in DNA damage- induced cell death decision.

Authors:  Tingzhe Sun; Chun Chen; Yuanyuan Wu; Shuai Zhang; Jun Cui; Pingping Shen
Journal:  BMC Bioinformatics       Date:  2009-06-22       Impact factor: 3.169

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