碱性单细胞凝胶(SCG)试验中使用蛋白酶K区分dna -蛋白和DNA-DNA交联

H. Hayashi, M. Imai, Y. Shindo
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引用次数: 1

摘要

采用碱性(pH>13) SCG法,用蛋白酶K (PK)对DNA进行裂解后处理,对DNA-蛋白交联和DNA-DNA交联进行区分,实验采用小鼠淋巴瘤L5178Y tk+/-细胞体外暴露于甲醛或顺铂。甲醛特异性诱导DNA-蛋白交联,而顺铂诱导链间和链内DNA交联。在裂解后不进行PK处理的情况下,甲醛诱导DNA迁移量呈剂量依赖性显著降低。在裂解后使用PK去除残留蛋白,阻止了DNA迁移的减少。相比之下,顺铂在溶解后无论是否进行PK处理,都能诱导尾矩减小。这些结果表明,裂解后用PK处理可以作为SCG测定中区分dna -蛋白和DNA-DNA交联的补充方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discrimination between DNA-protein and DNA-DNA crosslinks using proteinase K in the alkaline single cell gel (SCG) assay
The alkaline (pH>13) SCG assay, with post-lysis treatment of DNA with proteinase K (PK), to discriminate between DNA-protein and DNA-DNA crosslinks was evaluated using mouse lymphoma L5178Y tk+/- cells exposed in vitro to formaldehyde or cisplatinum. Formaldehyde specifically induces DNA-protein crosslinks, whereas cisplatinum induces inter- and intra-strand DNA crosslinks. In the absence of treatment with PK after lysis, formaldehyde induced a dose-dependent significant decrease in DNA migration. The use of PK after lysis to remove residual protein prevented the reduction in DNA migration. In contrast, cisplatinum induced a decrease in tail moment, with and without PK treatment after lysis. These results indicate that post-lysis treatment with PK can be expected as a supplementary method in the SCG assay to discriminate between DNA-protein and DNA-DNA crosslinks.
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