Sutherland Betsy M, Bennett Paula V, Sutherland John C, Laval Jacques
Biology Department, Brookhaven National Laboratory, Upton, New York 11973-5000, USA.
Radiat Res. 2002 Jun;157(6):611-6. doi: 10.1667/0033-7587(2002)157[0611:cddibx]2.0.co;2.
Although DNA DSBs are known to be important in producing the damaging effects of ionizing radiation in cells, bistranded clustered DNA damages-two or more oxidized bases, abasic sites or strand breaks on opposing DNA strands within a few helical turns-are postulated to be difficult to repair and thus to be critical radiation-induced lesions. Gamma rays can induce clustered damages in DNA in solution, and high-energy iron ions produce DSBs and oxidized pyrimidine clusters in human cells, but it was not known whether sparsely ionizing radiation can produce clustered damages in mammalian cells. We show here that X rays induce abasic clusters, oxidized pyrimidine clusters, and oxidized purine clusters in DNA in human cells. Non-DSB clustered damages comprise about 70% of the complex lesions produced in cells. The relative levels of specific cluster classes depend on the environment of the DNA.
虽然已知DNA双链断裂在产生电离辐射对细胞的损伤效应中很重要,但双股簇状DNA损伤(在几个螺旋圈内相对DNA链上的两个或更多个氧化碱基、无碱基位点或链断裂)被推测难以修复,因此是关键的辐射诱导损伤。γ射线可在溶液中诱导DNA产生簇状损伤,高能铁离子可在人类细胞中产生双链断裂和氧化嘧啶簇,但尚不清楚低线性能量传递辐射是否能在哺乳动物细胞中产生簇状损伤。我们在此表明,X射线可在人类细胞的DNA中诱导无碱基簇、氧化嘧啶簇和氧化嘌呤簇。非双链断裂簇状损伤约占细胞中产生的复杂损伤的70%。特定簇类别的相对水平取决于DNA的环境。