Base excision repair (BER), as initiated by at least seven different DNA gl
ycosylases or by enzymes that cleave DNA at abasic sites, executes the repa
ir of a wide variety of DNA damages. Many of these damages arise spontaneou
sly because DNA interacts with the cellular milieu, and so BER profoundly i
nfluences spontaneous mutation rates. In addition, BER provides significant
protection against the toxic and mutagenic effects of DNA damaging agents
present in the external environment, and as such is likely to prevent the a
dverse health effects of such agents. BER pathways have been studied in a w
ide variety of organisms (including yeasts) and here we review how these va
ried studies have shaped our current view of human BER. (C) 2000 Published
by Elsevier Science B.V.