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On the Chemical Yield of Base Lesions Strand Breaks and Clustered Damage Generated in Plasmid DNA by the Direct Effect of X Rays

机译:X射线直接作用下质粒DNA中碱基病变链断裂和簇状损伤的化学产率

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摘要

The purpose of this study was to determine the yield of DNA base damages, deoxyribose damage, and clustered lesions due to the direct effects of ionizing radiation and to compare these with the yield of DNA trapped radicals measured previously in the same pUC18 plasmid. The plasmids were prepared as films hydrated in the range 2.5 < Γ < 22.5 mol water/mol nucleotide. Single-strand breaks (SSBs) and double-strand breaks (DSBs) were detected by agarose gel electrophoresis. Specific types of base lesions were converted into SSBs and DSBs using the base-excision repair enzymes endonuclease III (Nth) and formamidopyrimidine-DNA glycosylase (Fpg). The yield of base damage detected by this method displayed a strikingly different dependence on the level of hydration (Γ) compared with that for the yield of DNA trapped radicals; the former decreased by 3.2 times as Γ was varied from 2.5 to 22.5 and the later increased by 2.4 times over the same range. To explain this divergence, we propose that SSB yields produced in plasmid DNA by the direct effect cannot be analyzed properly with a Poisson process that assumes an average of one strand break per plasmid and neglects the possibility of a single track producing multiple SSBs within a plasmid. The yields of DSBs, on the other hand, are consistent with changes in free radical trapping as a function of hydration. Consequently, the composition of these clusters could be quantified. Deoxyribose damage on each of the two opposing strands occurs with a yield of 3.5 ± 0.5 nmol/J for fully hydrated pUC18, comparable to the yield of 4.1 ± 0.9 nmol/J for DSBs derived from opposed damages in which at least one of the sites is a damaged base.
机译:这项研究的目的是确定由于电离辐射的直接作用引起的DNA碱基损伤,脱氧核糖损伤和簇状损伤的产生,并将这些与先前在同一pUC18质粒中测定的DNA捕获自由基的产生进行比较。将质粒制备为水合膜,其水合度范围为2.5 <Γ<22.5 mol水/ mol核苷酸。通过琼脂糖凝胶电泳检测单链断裂(SSB)和双链断裂(DSB)。使用碱基切除修复酶核酸内切酶III(Nth)和甲酰嘧啶-DNA糖基化酶(Fpg)将特定类型的碱基病变转化为SSB和DSB。通过这种方法检测到的碱基破坏的产量与水合水平(Γ)的依赖性相比,与对DNA捕获自由基的产量有着显着不同的依赖性。在相同范围内,当Γ从2.5变为22.5时,前者下降了3.2倍,而后者则增长了2.4倍。为了解释这种差异,我们建议不能通过泊松过程来正确分析直接作用在质粒DNA中产生的SSB产量,该泊松过程假定每个质粒平均有一条链断裂,而忽略了在一条质粒中单条轨道产生多个SSB的可能性。 。另一方面,DSB的产率与自由基捕获随水合作用的变化一致。因此,可以量化这些簇的组成。完全相反的pUC18的两个相对链的每一个发生脱氧核糖破坏,产率为3.5±0.5 nmol / J,与源自对立破坏的DSB的4.1±0.9 nmol / J的产率相当,其中至少一个位点是一个损坏的基地。

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