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. 1985 Dec 20;13(24):9011–9029. doi: 10.1093/nar/13.24.9011

Malondialdehyde precursors in gamma-irradiated DNA, deoxynucleotides and deoxynucleosides.

M F Janicek, W A Haseltine, W D Henner
PMCID: PMC318968  PMID: 4080556

Abstract

Gamma-irradiation of DNA, deoxynucleosides, or deoxynucleotides produces material that reacts with thiobarbituric acid to form a chromophore with maximum absorbance at 532 nm. This material is not malondialdehyde. We have identified a new radiation product (thymin-1'-yl)-propenal as the TBA-reactive product of gamma-irradiation of thymidine. Thymine-propenal has been described by other investigators as a product of bleomycin-treatment of DNA. Irradiation of thymidine nucleotides produces phosphorylated precursors to thymine-propenal. Studies of the requirements for formation of TBA-reactivity indicate a mechanism involving reaction of a free radical with the deoxyribose moiety and molecular oxygen. On the basis of these results it is proposed that gamma-irradiation produces TBA-reactive material in DNA by the same reaction sequence in which bleomycin catalyzes the formation of base-propenals in DNA. Bleomycin and gamma-irradiation differ in the extent to which the sequence proceeds to completion with release of free base-propenals.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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