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Lack of interference of DNA single-strand breaks with the measurement of double-strand breaks in mammalian cells using the neutral filter elution assay.

机译:使用中性滤膜洗脱测定法测量哺乳动物细胞中的双链断裂时DNA单链断裂不会受到干扰。

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摘要

In this study, the effect of DNA single strand breaks (ssb) on the neutral (pH 9.6) filter elution of DNA from Chinese hamster ovary (CHO K1) cells containing DNA double strand breaks (dsb) was investigated. Protein associated ssb were induced by the inhibition of DNA topoisomerase I with camptothecin (cpt). Protein associated dsb were introduced by treating cells with the DNA topoisomerase II poison; etoposide (VP-16). Protein associated ssb and dsb were converted to ssb and dsb by proteinase K present in the lysis solution. In some experiments dsb were generated by the restriction endonuclease Pvu II. It was found that elution of DNA in the presence and absence of ssb was similar under neutral conditions. This finding is consistent with the view that the fast component of the bi-phasic repair kinetics observed in irradiated mammalian cells with the neutral filter elution technique is not attributable to the interference of ssb with the measurement of dsb, and thus suggests that the two components of repair observed with the neutral filter elution elution technique may represent two different types of dsb or modes of repair of dsb.
机译:在这项研究中,研究了DNA单链断裂(ssb)对含有DNA双链断裂(dsb)的中国仓鼠卵巢(CHO K1)细胞中DNA的中性(pH 9.6)过滤器洗脱的影响。喜树碱(cpt)通过抑制DNA拓扑异构酶I诱导蛋白相关的ssb。通过用DNA拓扑异构酶II毒物处理细胞来引入蛋白质相关的dsb;依托泊苷(VP-16)。通过裂解溶液中存在的蛋白酶K将与蛋白质相关的ssb和dsb转化为ssb和dsb。在一些实验中,dsb是由限制性核酸内切酶Pvu II产生的。发现在中性条件下,存在和不存在ssb时DNA的洗脱都是相似的。这一发现与以下观点相一致:使用中性滤膜洗脱技术在辐照的哺乳动物细胞中观察到的双相修复动力学的快速成分不归因于ssb对dsb的测量干扰,因此表明这两个成分用中性过滤器洗脱洗脱技术观察到的修复可能代表两种不同类型的dsb或dsb的修复模式。

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