4.8 Article

Enhanced DNA repair through droplet formation and p53 oscillations

Journal

CELL
Volume 185, Issue 23, Pages 4394-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2022.10.004

Keywords

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Funding

  1. European Research Council (ERC) under the European Union [740704]
  2. Taiwan National Science and Technology Council [111-2311-B-001-012]
  3. Academia Sinica [AS-DA-108-L01]
  4. Carlsberg Foundation [CF20-0621]
  5. Lundbeck Foundation [R347-2020-2250]
  6. Independent Research Fund Denmark [9040-00116B]
  7. Novo Nordisk Foundation [NNF20OC0064978]

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This study investigates the dynamic signaling in the repair process of DNA damage in cells, revealing that the oscillatory dynamics of the transcription factor p53 optimize the repair efficiency by forming sub-compartments.
Living organisms are constantly exposed to DNA damage, and optimal repair is therefore crucial. A charac-teristic hallmark of the response is the formation of sub-compartments around the site of damage, known as foci. Following multiple DNA breaks, the transcription factor p53 exhibits oscillations in its nuclear concen-tration, but how this dynamics can affect the repair remains unknown. Here, we formulate a theory for foci formation through droplet condensation and discover how oscillations in p53, with its specific periodicity and amplitude, optimize the repair process by preventing Ostwald ripening and distributing protein material in space and time. Based on the theory predictions, we reveal experimentally that the oscillatory dynamics of p53 does enhance the repair efficiency. These results connect the dynamical signaling of p53 with the micro-scopic repair process and create a new paradigm for the interplay of complex dynamics and phase transi-tions in biology.

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