Abstract
The treatment of transfer ribonucleic acids (tRNAs) with ozone and subsequent treatment with aniline-acetate (pH 4.5) resulted in the internucleotidic bond cleavage of tRNAs. Sequence analysis of the fragments obtained showed that the internucleotidic bond-cleavage occurred at the guanine residues modified with ozone, and the most susceptible sites were those in consecutive sequences of guanine residues, such as -GpGpGpGp- and -GpGpm1Gp-in tRNAPro.