Nucleic Acids Research, 2001, Vol. 29, No. 6 1341-1351
© 2001 Oxford University Press
Chromatin-bound PCNA complex formation triggered by DNA damage occurs independent of the ATM gene product in human cells
Department of Radiation Oncology, Center for Radiological Research, College of Physicians and Surgeons, Columbia University, VC-11, Room 243, 630 West, 168th Street, New York, NY 10032, USA
Proliferating cell nuclear antigen (PCNA), a processivity factor for DNA polymerases 
and 
, is involved in DNA replication as well as in diverse DNA repair pathways. In quiescent cells, UV light-induced bulky DNA damage triggers the transition of PCNA from a soluble to an insoluble chromatin-bound form, which is intimately associated with the repair synthesis by polymerases and . In this study, we investigated the efficiency of PCNA complex formation in response to ionizing radiation-induced DNA strand breaks in normal and radiation-sensitive Ataxia telangiectasia (AT) cells by immunofluorescence and western blot techniques. Exposure of normal cells to 
-rays rapidly triggered the formation of PCNA foci in a dose-dependent manner in the nuclei and the PCNA foci (40–45%) co-localized with sites of repair synthesis detected by bromodeoxyuridine labeling. The chromatin-bound PCNA gradually declined with increasing post-irradiation times and almost reached the level of unirradiated cells by 6 h. The PCNA foci formed after -irradiation was resistant to high salt extraction and the chromatin association of PCNA was lost after DNase I digestion. Interestingly, two radiosensitive primary fibroblast cell lines, derived from AT patients harboring homozygous mutations in the ATM gene, displayed an efficient PCNA redistribution after -irradiation. We also analyzed the PCNA complex induced by a radiomimetic agent, Bleomycin (BLM), which produces predominantly single- and double-strand DNA breaks. The efficiency and the time course of PCNA complex induced by BLM were identical in both normal and AT cells. Our study demonstrates for the first time that the ATM gene product is not required for PCNA complex assembly in response to DNA strand breaks. Additionally, we observed an increased interaction of PCNA with the Ku70 and Ku80 heterodimer after DNA damage, suggestive of a role for PCNA in the non-homologous end-joining repair pathway of DNA strand breaks.
* To whom correspondence should be addressed. Tel: +1 212 305 0845; Fax: +1 212 305 3229; Email: ab836{at}columbia.edu Correspondence may also be addressed to Charles R. Geard. Tel: +1 212 305 0845; Fax: +1 212 305 3229; Email: crg4{at}columbia.edu
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