DNA damage induced by the direct effect of radiation

• Published in: Radiation physics and chemistry (Oxford, England : 1993) Vol. 77; no. 10; pp. 1280 - 1285
• Main Authors: Yokoya, A., Shikazono, N., Fujii, K., Urushibara, A., Akamatsu, K., Watanabe, R.
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.10.2008
• Subjects: Clustered damage; Direct effects of radiation; DNA strand break; Glycosylases; LET; Glycosylases; LET; Direct effects of radiation; Clustered damage; DNA strand break
• ISSN: 0969-806X; 1879-0895
• DOI: 10.1016/j.radphyschem.2008.05.021

We have studied the nature of DNA damage induced by the direct effect of radiation. The yields of single- (SSB) and double-strand breaks (DSB), base lesions and clustered damage were measured using the agarose gel electrophoresis method after exposing to various kinds of radiations to a simple model DNA molecule, fully hydrated closed-circular plasmid DNA (pUC18). The yield of SSB does not show significant dependence on linear energy transfer (LET) values. On the other hand, the yields of base lesions revealed by enzymatic probes, endonuclease III (Nth) and formamidopyrimidine DNA glycosylase (Fpg), which excise base lesions and leave a nick at the damage site, strongly depend on LET values. Soft X-ray photon (150 kVp) irradiation gives a maximum yield of the base lesions detected by the enzymatic probes as SSB and clustered damage, which is composed of one base lesion and proximate other base lesions or SSBs. The clustered damage is visualized as an enzymatically induced DSB. The yields of the enzymatically additional damages strikingly decrease with increasing levels of LET. These results suggest that in higher LET regions, the repair enzymes used as probes are compromised because of the dense damage clustering. The studies using simple plasmid DNA as a irradiation sample, however, have a technical difficulty to detect multiple SSBs in a plasmid DNA. To detect the additional SSBs induced in opposite strand of the first SSB, we have also developed a novel technique of DNA-denaturation assay. This allows us to detect multiply induced SSBs in both strand of DNA, but not induced DSB.