Chemistry of the Bleomycin-Induced Alkali-Labile DNA Lesion
journal contributionposted on 16.09.1999 by Mariko Aso, Mitsumasa Kondo, Hiroshi Suemune, Sidney M. Hecht
Any type of content formally published in an academic journal, usually following a peer-review process.
Treatment of B-form DNA with the antitumor antibiotic bleomycin in the presence of Fe2+ and O2 affords both DNA strand scission and the formation of alkali-labile lesions, the proportion of which is quite sensitive to the concentration of O2 present. The alkali-labile lesions can undergo fragmentation cleanly in the presence of n-butylamine to afford DNA fragments containing 5‘- and 3‘-phosphate termini at the site of the alkali-labile lesion. The mechanism of decomposition of the alkali-labile lesion was studied, leading to identification of a putative intermediate that is converted readily to an (oligo)nucleotide 3‘-phosphate in the presence of n-BuNH2, as well as the identification of the byproduct of the fragmentation reaction containing the carbon atoms originally present within the alkali-labile lesion.