Cytosine to thymine transitions are among the most common types of mut
ations produced by oxygen damage to DNA. One possible mechanism for th
ese transitions is deamination of cytosine to uracil. Using both a for
ward mutation assay as well as a reversion assay specific for damage t
o cytosines we show that direct deamination to uracil does not play a
significant role in mutagenesis induced by reactive oxygen free radica
ls. In contrast, lesions sensitive to repair by E. coli endonuclease I
II play a major role in oxidative mutagenesis as evidenced by the abil
ity of endonuclease III to modulate the extent of mutagenesis that res
ults from exposure of DNA to oxygen free radicals.