p21-induced cycle arrest in G1 protects cells from apoptosis induced by UV-irradiation or RNA polymerase II blockage

Cells expressing the R273H mutant of p53, which lacks sequence specific DNA binding capacity, do not undergo cell cycle arrest in G(1) following exposure to ionizing or UV radiation because of their inability to induce p21(Waf1/Cip1), a cyclin-dependent kinase inhibitor and downstream mediator of p53-dependent DNA damage-induced growth arrest. Following UV-irradiation or treatment with an inhibitor of RNA pol II, we observed a rapid induction of the apoptotic process, as evidenced by DNA fragmentation and the proteolytic cleavage of poly(ADP-ribose) polymerase. Using mimosine, a p21(Waf1/Cip1) inducer that bypasses the requirement for transcriptional transactivation by p53, we demonstrated that a G(1) cell cycle arrest can prevent apoptosis following UV-irradiation or treatment with an RNA polymerase II inhibitor, Serum starvation, which also synchronized cells in G(1) but did not induce p21(Waf1/Cip1), did not protect cells from apoptosis, These results demonstrate that restoring a late G(1) checkpoint by inducing p21(Waf1/Cip1) expression can protect cells from DNA damage induced apoptosis, Our results suggest that p21(Waf2/Cip1) can interrupt the apoptotic process at a point downstream from p53 accumulation but upstream from caspase-3 activation.