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Molecular and Cellular Biology, September 2000, p. 6695-6703, Vol. 20, No. 18
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

DNA Excision Repair and DNA Damage-Induced Apoptosis Are Linked to Poly(ADP-Ribosyl)ation but Have Different Requirements for p53

Ralph Beneke,1 Christoph Geisen,1 Branko Zevnik,1 Thomas Bauch,2 Wolfgang-Ulrich Müller,2 Jan-Heiner Küpper,3 and Tarik Möröy1,*

Institut für Zellbiologie (Tumorforschung), IFZ,1 and Institut für Medizinische Strahlenbiologie,2 Universitätsklinikum Essen, D-45122 Essen, and Institut für Pathologie, Universitätsklinikum Tübingen, D-72076 Tübingen,3 Germany

Received 17 April 2000/Returned for modification 1 June 2000/Accepted 9 June 2000

Poly(ADP-ribose) polymerase (PARP) is a DNA binding zinc finger protein that catalyzes the transfer of ADP-ribose residues from NAD+ to itself and different chromatin constituents, forming branched ADP-ribose polymers. The enzymatic activity of PARP is induced upon DNA damage and the PARP protein is cleaved during apoptosis, which suggested a role of PARP in DNA repair and DNA damage-induced cell death. We have generated transgenic mice that lack PARP activity in thymocytes owing to the targeted expression of a dominant negative form of PARP. In the presence of single-strand DNA breaks, the absence of PARP activity correlated with a strongly increased rate of apoptosis compared to cells with intact PARP activity. We found that blockage of PARP activity leads to a drastic increase of p53 expression and activity after DNA damage and correlates with an accelerated onset of Bax expression. DNA repair is almost completely blocked in PARP-deficient thymocytes regardless of p53 status. We found the same increased susceptibility to apoptosis in PARP null mice, a similar inhibition of DNA repair kinetics, and the same upregulation of p53 in response to DNA damage. Thus, based on two different experimental in vivo models, we identify a direct, p53-independent, functional connection between poly(ADP-ribosyl)ation and the DNA excision repair machinery. Furthermore, we propose a p53-dependent link between PARP activity and DNA damage-induced cell death.


* Corresponding author. Mailing address: Institut für Zellbiologie (Tumorforschung), IFZ, Universitätsklinikum Essen, Virchowstrasse 173, D-45122 Essen, Germany. Phone: 49 (201) 723-3380. Fax: 49 (201) 723-5904. E-mail: moeroey{at}uni-essen.de.


Molecular and Cellular Biology, September 2000, p. 6695-6703, Vol. 20, No. 18
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



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