Haq S, Natori S, Sekimizu K
Faculty of Pharmaceutical Sciences, University of Tokyo.
J Biochem. 1993 May;113(5):620-4. doi: 10.1093/oxfordjournals.jbchem.a124092.
In general, covalently-closed circular DNAs that are relaxed by DNA topoisomerase I at higher temperatures are more negatively (or less positively) supercoiled when analyzed at the same temperature. We found that in the presence of ethidium bromide the reaction products were less negatively supercoiled at higher temperatures. Consequently, the linking number of substrate DNA changed reversibly with temperature-shift: DNA relaxation occurred on temperature shift-up, and re-supercoiling on temperature shift-down. Analyses of the migration of covalently closed circular DNA on agarose gel electrophoresis and of the fluorescence intensity of ethidium bromide bound to DNA indicated decrease in binding of the drug to DNA at higher temperatures. Thus, the thermal effects on the topology of the reaction products of mouse DNA topoisomerase I in the presence of ethidium bromide can be explained by the temperature-sensitive interaction of the drug with DNA.
一般来说,在较高温度下被DNA拓扑异构酶I松弛的共价闭合环状DNA,在相同温度下分析时,其负超螺旋程度更高(或正超螺旋程度更低)。我们发现,在溴化乙锭存在的情况下,反应产物在较高温度下负超螺旋程度较低。因此,底物DNA的连接数随温度变化而可逆地改变:温度升高时发生DNA松弛,温度降低时重新超螺旋。对共价闭合环状DNA在琼脂糖凝胶电泳上的迁移以及与DNA结合的溴化乙锭荧光强度的分析表明,在较高温度下药物与DNA的结合减少。因此,在溴化乙锭存在的情况下,温度对小鼠DNA拓扑异构酶I反应产物拓扑结构的影响可以通过药物与DNA的温度敏感相互作用来解释。