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Nucleic Acids Research, 2000, Vol. 28, No. 17 3294-3300
© 2000 Oxford University Press

In vivo repair of methylation damage in Aag 3-methyladenine DNA glycosylase null mouse cells

Stephen A. Smith and Bevin P. Engelward*

Division of Bioengineering and Environmental Health, 77 Massachusetts Avenue, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

3-Methyladenine (3MeA) DNA glycosylases initiate base excision repair by removing 3MeA. These glycosylases also remove a broad spectrum of spontaneous and environmentally induced base lesions in vitro. Mouse cells lacking the Aag 3MeA DNA glycosylase (also known as the Mpg, APNG or ANPG DNA glycosylase) are susceptible to 3MeA-induced S phase arrest, chromosome aberrations and apoptosis, but it is not known if Aag is solely responsible for repair of 3MeA in vivo. Here we show that in Aag–/– cells, 3MeA lesions disappear from the genome slightly faster than would be expected by spontaneous depurination alone, suggesting that there may be residual repair of 3MeA. However, repair of 3MeA is at least 10 times slower in Aag–/– cells than in Aag+/+ cells. Consequently, 24 h after exposure to [3H]MNU, 30% of the original 3MeA burden is intact in Aag–/– cells, while 3MeA is undetectable in Aag+/+ cells. Thus, Aag is the major DNA glycosylase for 3MeA repair. We also investigated the in vivo repair kinetics of another Aag substrate, 7-methylguanine. Surprisingly, 7-methylguanine is removed equally efficiently in Aag+/+ and Aag–/– cells, suggesting that another DNA glycosylase acts on lesions previously thought to be repaired by Aag.

* To whom correspondence should be addressed. Tel: +1 617 258 0260; Fax: +1 617 258 0499; Email: bevin@mit.edu


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