Bell A, Kittler L, Löber G, Zimmer C
Institut für Molekulare Biotechnologie e.V., Jena, Germany.
Invest New Drugs. 1996;13(4):271-84. doi: 10.1007/BF00873133.
This report deals with the cleavage reaction of calf thymus (CT) topoisomerase II with oligonucleotides containing one main cleavage site and adjacent binding sites for minor groove binders. The sequences of the oligonucleotides were derived from a pBR 322 sequence, which contains one main topoisomerase II cleavage site. The cleavage reaction was performed under increasing concentrations of minor groove binders and it showed characteristic inhibition dependences of topoisomerase II to the binding sites and to the binding length of the minor groove binders. The extension of the minor groove binder length on DNA from 4 to 10 base pairs (bp) by netropsin and bis-netropsin, respectively, causes a strong increase of the topoisomerase II cleavage inhibition. The same is observed by the introduction of a second minor groove binder sequence symmetrically positioned around the topoisomerase II main cleavage site. The combination of two different minor groove binders can lead to an increased topoisomerase II inhibition but also to a prevention of total inhibition as shown with chromomycin A3 and distamycin A at concentrations of 0.1 and 0.25 microM, respectively.
本报告涉及小牛胸腺(CT)拓扑异构酶II与含有一个主要切割位点以及小沟结合剂相邻结合位点的寡核苷酸的切割反应。这些寡核苷酸的序列源自pBR 322序列,该序列包含一个主要的拓扑异构酶II切割位点。切割反应在小沟结合剂浓度不断增加的情况下进行,结果显示拓扑异构酶II对结合位点以及小沟结合剂的结合长度具有典型的抑制依赖性。分别通过纺锤菌素和双纺锤菌素将DNA上小沟结合剂的长度从4个碱基对(bp)延长至10个碱基对,会导致拓扑异构酶II切割抑制作用显著增强。在拓扑异构酶II主要切割位点周围对称引入第二个小沟结合剂序列时也观察到同样的现象。两种不同小沟结合剂的组合可能会增强拓扑异构酶II的抑制作用,但也可能会防止完全抑制,如分别在浓度为0.1和0.25微摩尔的放线菌素A3和偏端霉素A的实验中所示。