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DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression

Authors: Alexis R. Barr; Chris Bakal; Bela Novak; Francesca Butera; Jörg Mansfeld; Sam Cooper; Sam Cooper; +2 Authors

DNA damage during S-phase mediates the proliferation-quiescence decision in the subsequent G1 via p21 expression

Abstract

AbstractFollowing DNA damage caused by exogenous sources, such as ionizing radiation, the tumour suppressor p53 mediates cell cycle arrest via expression of the CDK inhibitor, p21. However, the role of p21 in maintaining genomic stability in the absence of exogenous DNA-damaging agents is unclear. Here, using live single-cell measurements of p21 protein in proliferating cultures, we show that naturally occurring DNA damage incurred over S-phase causes p53-dependent accumulation of p21 during mother G2- and daughter G1-phases. High p21 levels mediate G1 arrest via CDK inhibition, yet lower levels have no impact on G1 progression, and the ubiquitin ligases CRL4Cdt2 and SCFSkp2 couple to degrade p21 prior to the G1/S transition. Mathematical modelling reveals that a bistable switch, created by CRL4Cdt2, promotes irreversible S-phase entry by keeping p21 levels low, preventing premature S-phase exit upon DNA damage. Thus, we characterize how p21 regulates the proliferation-quiescence decision to maintain genomic stability.

Keywords

Cyclin-Dependent Kinase Inhibitor p21, 570, STOCHASTIC SIMULATION, Science, Green Fluorescent Proteins, 610, Article, Genomic Instability, Cell Line, S Phase, UBIQUITIN LIGASE, FRAGILE SITES, Gene Knockout Techniques, HUMAN FIBROBLASTS, CELL-CYCLE, Humans, Cell Proliferation, G(1) ARREST, Microscopy, Science & Technology, Microscopy, Confocal, Q, G1 Phase, Cell Cycle Checkpoints, TUMOR SUPPRESSION, Multidisciplinary Sciences, Cell Tracking, Confocal, CYCLIN-DEPENDENT KINASES, CDK INHIBITOR P21, Science & Technology - Other Topics, REPLICATION FORK, Tumor Suppressor Protein p53, Cell Division, DNA Damage

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    333
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 0.1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
333
Top 0.1%
Top 1%
Top 0.1%
Green
gold