Andersen A H, Gocke E, Bonven B J, Nielsen O F, Westergaard O
Nucleic Acids Res. 1985 Mar 11;13(5):1543-57. doi: 10.1093/nar/13.5.1543.
Topoisomerase I is in situ associated with DNaseI hypersensitive sites located in the promotor and terminator regions of the extrachromosomal rDNA in Tetrahymena thermophila at sites with sequences fitting the motif (sequence in text) Reconstitution experiments with purified topoisomerase I and cloned fragments of rDNA demonstrate that the enzyme exhibits the same binding and cleavage properties on naked DNA. These observations are striking as topoisomerase I previously has been found to exhibit low sequence specificity. The specific binding of the enzyme has an absolute requirement for divalent cations with a preference for Ca2+. The strong binding to the hexadecamer has been characterized by competition experiments, and it has been used to determine the molecular weight of the enzyme.
拓扑异构酶I原位与嗜热四膜虫染色体外rDNA启动子和终止子区域中对基序(文本中的序列)具有匹配序列的位点处的DNaseI超敏位点相关。用纯化的拓扑异构酶I和rDNA克隆片段进行的重组实验表明,该酶在裸露的DNA上表现出相同的结合和切割特性。这些观察结果令人惊讶,因为此前发现拓扑异构酶I表现出低序列特异性。该酶的特异性结合对二价阳离子有绝对要求,优先选择Ca2+。通过竞争实验对其与十六聚体的强结合进行了表征,并用于确定该酶的分子量。