bioRxivCancer BiologyPreprint
Dynamics of the p53 response to ionizing and ultraviolet radiation
Elizabeth A. FedakiD, Frederick R. AdleriD, Erin L. Young, Lisa M. AbeggleniD, Joshua D. Schiffman
Abstract
The tumor suppressor protein p53 compiles information about cellular stressors to make decisions on whether the cell should survive or undergo apoptosis. However, the p53 response depends on the source of damage, displaying a digital oscillatory response after ionizing radiation (IR) damage and a proportional non-oscillatory response following UV damage. We propose a mathematical model that qualitatively replicates this observed behavior. The difference in p53 dynamics in the model results from two mechanisms: IR damage is fully detected minutes after exposure while UV damage is detected over several hours; and the p53-controlled transcriptional response is dominated by inactive p53 following UV damage. In particular, we hypothesize that an unidentified positive feedback loop controlled by inactive p53 is required to maintain the qualitative high p53 response to UV damage. This work proposes an explanation for two distinct responses of p53 to DNA damage and how each response can lead to cell cycle arrest or apoptosis.\n\nAuthor summaryWe propose a mathematical model hypothesizing how the tumor suppressor protein p53 produces two contrasting dynamical responses in response to different types of DNA damage. In particular, we predict the existence of a positive feedback loop controlled by the inactive form of p53, which allows the cell to respond to slowly detected damage. The existence of differing dynamic responses by p53 has implications for our understanding of tumor development and possibly p53-related therapeutic strategies.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- What p53 sees: ATM and ATR activation through crosstalk between DNA damage response pathways
Elizabeth A. Fedak, Frederick R. Adler, … Joshua David Schiffman·Bulletin of Mathematical BiologyPeer-reviewed·Mar 11, 2021
- Intricate Dynamical Cross-Talk Between p53 Protein and Cell Cycle Regulators Governs Mammalian Cell Fate
Kajal Charan, Sandip Kar·bioRxiv·Jun 10, 2026
- p53 pro-apoptotic activity is regulated by the G2/M promoting factor Cdk1 in response to DNA damage
Mireya Ruiz-Losada, Raul González, … Carlos Estella·bioRxiv·Feb 13, 2021
- Long-term p21 and p53 trends regulate the frequency of mitosis events and cell cycle arrest
Anh Phong Tran, Christopher John Tralie, … Allen Tannenbaum·bioRxiv·Aug 17, 2021
- p53 controls choice between apoptotic and non-apoptotic death following DNA damage
M. E. Honeywell, M. S. Isidor, … M. J. Lee·bioRxiv·Jan 17, 2023
- Both DNA binding domains of p53 are required for its ultra rapid recruitment to sites of UV damage
Y.-H. Wang, T. Ho, … D. Lane·bioRxiv·Feb 9, 2020