Krisch R E, Flick M B, Trumbore C N
Department of Radiation Oncology, University of Pennsylvania School of Medicine, Philadelphia 19104.
Radiat Res. 1991 May;126(2):251-9.
Using an electrophoresis assay system developed in our laboratory, we have simultaneously measured single- and double-strand DNA breaks (SSBs and DSBs) induced by gamma radiation in small SV40 viral DNA molecules, under conditions of greatly varying radical scavenger concentration and DNA configuration. In our experiments with aqueous solutions of SV40 DNA, we observe that SSB induction is linear with dose (one-hit response), over the entire hydroxyl scavenger efficiency range examined, from approximately 0 to 5 x 10(9) s-1, while DSB induction shifts from having a major quadratic component (two-hit response) at very low scavenger efficiencies to nearly pure linear for efficiencies greater than 10(7) s-1. The mean ratio of SSBs to one-hit DSBs remains relatively constant with increasing scavenger efficiency, decreasing from about 100:1 to 40:1 as the scavenger efficiency increases from 2 x 10(5) s-1 to 5 x 10(9) s-1, and the absolute induction efficiencies for breaks decrease by three orders of magnitude. This decrease takes place primarily at scavenger efficiencies above 1 x 10(8) s-1. Irradiation of intranuclear SV40 minichromosomes induces SSBs and DSBs at nearly the same efficiencies as does irradiation of free DNA at the highest scavenger concentrations examined, and at only about twice the efficiencies observed at -75 degrees C, where direct effects are believed to predominate. Our observations that the linear-quadratic mix of the dose-response curve for DSBs depends critically on scavenger efficiency may help to clarify the considerable confusion in the literature on the shape of such curves. Our observations of a relatively constant ratio between one-hit SSBs and DSBs at low and moderate scavenger efficiencies are in agreement with the recent hypothesis of Siddiqi and Bothe (Radiat. Res. 112, 449-463 (1987)) that, contrary to widely and long-held beliefs, the formation by indirect effects of a one-hit DSB in DNA occurs under these conditions predominantly by a mechanism involving a single OH radical, with a presumed radical transfer between complementary DNA strands. In contrast, our results for strongly protective conditions are not consistent with this hypothesis, but are consistent with the predictions of Ward's hypothesis (Radiat. Res. 86, 185-195, (1981)) that one-hit DSBs from indirect effects are produced predominantly by local clusters of OH radicals from single energy deposition events (locally multiply damaged sites) rather than by single OH radicals.(ABSTRACT TRUNCATED AT 400 WORDS)
我们使用在本实验室开发的电泳分析系统,在自由基清除剂浓度和DNA构型变化极大的条件下,同时测量了γ辐射在小型SV40病毒DNA分子中诱导产生的单链和双链DNA断裂(SSB和DSB)。在我们对SV40 DNA水溶液的实验中,我们观察到,在所研究的整个羟基清除剂效率范围内,从约0至5×10⁹ s⁻¹,SSB的诱导与剂量呈线性关系(单 hit 响应),而DSB的诱导则从极低清除剂效率下的主要二次成分(双 hit 响应)转变为清除剂效率大于10⁷ s⁻¹时几乎纯的线性关系。随着清除剂效率的增加,SSB与单 hit DSB的平均比率保持相对恒定,当清除剂效率从2×10⁵ s⁻¹增加到5×10⁹ s⁻¹时,该比率从约100:1降至40:1,并且断裂的绝对诱导效率降低了三个数量级。这种降低主要发生在清除剂效率高于1×10⁸ s⁻¹时。在核内SV40微型染色体的辐照实验中,在所研究的最高清除剂浓度下,诱导产生SSB和DSB的效率与游离DNA辐照时几乎相同,并且仅约为在 -75℃观察到的效率的两倍,在 -75℃时据信直接效应占主导。我们观察到DSB剂量响应曲线的线性 - 二次混合严重依赖于清除剂效率,这可能有助于澄清文献中关于此类曲线形状的相当大的混乱。我们观察到在低和中等清除剂效率下单 hit SSB和DSB之间的比率相对恒定,这与Siddiqi和Bothe(《辐射研究》112, 449 - 463 (1987))最近的假设一致,即与长期广泛持有的观点相反,在这些条件下,DNA中通过间接效应形成单 hit DSB主要是通过涉及单个OH自由基的机制,推测自由基在互补DNA链之间转移。相比之下,我们在强保护条件下的结果与该假设不一致,但与Ward假设(《辐射研究》86, 185 - 195, (1981))的预测一致,即间接效应产生的单 hit DSB主要由单个能量沉积事件产生的OH自由基局部簇(局部多重损伤位点)而非单个OH自由基产生。(摘要截短于400字)