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UV irradiation triggers ubiquitin-dependent degradation of p21(WAF1) to promote DNA repair.

Cell | Sep 5, 2003

p53-mediated increase in cyclin-dependent kinase inhibitor p21(WAF1) protein is thought to be the major mediator of cell cycle arrest after DNA damage. Previously p21 protein levels have been reported to increase or to decrease after UV irradiation. We show that p21 protein is degraded after irradiation of a variety of cell types with low but not high doses of UV. Cell cycle arrest occurs despite p21 degradation via Tyr(15) inhibitory phosphorylation of cdk2 and differs from the classical p21-dependent checkpoint elicited by ionizing radiation. In contrast to the basal turnover of p21, degradation of p21 switches to ubiquitin/Skp2-dependent proteasome pathway following UV irradiation. ATR activation after UV irradiation is essential for signaling p21 degradation. Finally, UV-induced p21 degradation is essential for optimal DNA repair. These results provide novel insight into regulation of p21 protein and its role in the cellular response to DNA damage.

Pubmed ID: 13678583 RIS Download

Mesh terms: 3T3 Cells | Animals | Caffeine | Cell Cycle | Cell Cycle Proteins | Cyclin-Dependent Kinase Inhibitor p21 | Cyclins | Cycloheximide | DNA Damage | DNA Repair | Detergents | Dose-Response Relationship, Drug | HeLa Cells | Humans | Mice | Microscopy, Fluorescence | Models, Biological | Octoxynol | Phosphorylation | Precipitin Tests | Protein Synthesis Inhibitors | S-Phase Kinase-Associated Proteins | Signal Transduction | Temperature | Time Factors | Transfection | Tyrosine | Ubiquitin | Ultraviolet Rays

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Associated grants

  • Agency: NCI NIH HHS, Id: CA74435
  • Agency: NCI NIH HHS, Id: CA92321

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