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Thymine lesions produced by ionizing radiation in double-stranded DNA

Journal Article · · Biochemistry; (United States)
DOI:https://doi.org/10.1021/bi00336a032· OSTI ID:6255698
A DNA glycosylase which catalyzes the release of thymine residues damaged by ring saturation, fragmentation, or ring contraction from double-stranded DNA has been used to characterize such base derivatives in gamma-irradiated DNA. It is shown by chromatographic analysis that irradiation of DNA in neutral solution generates the ring-saturated forms cis-thymine glycol, trans-thymine glycol, and a monohydroxydihydrothymine, probably 6-hydroxy-5,6-dihydrothymine. The latter compound is only observed after irradiation under hypoxic conditions. The ring-contracted thymine derivative 5-hydroxy-5-methylhydantoin is also formed, and it is the major lesion after irradiation of DNA under O2. Ring-fragmented products such as methyltartronylurea were only generated in small quantities. Isolation and analysis of the DNA from gamma-irradiated human cells also revealed the formation of ring-saturated thymine derivatives, but 5-hydroxy-5-methylhydantoin was not found in this case.
Research Organization:
Imperial Cancer Research Fund, London, England
OSTI ID:
6255698
Journal Information:
Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 15; ISSN BICHA
Country of Publication:
United States
Language:
English