Camilloni G, Caserta M, Amadei A, Di Mauro E
Dipartimento di Genetica e Biologia Molecolare, Università di Roma La Sapienza, Italy.
Biochim Biophys Acta. 1991 Dec 2;1129(1):73-82. doi: 10.1016/0167-4781(91)90214-7.
The analysis of the sites which are cleaved constitutively and preferentially by eukaryotic DNA topoisomerase I on two intrinsically curved DNAs reveals the conformational features that provoke the cleavage reaction on the curve-inducing sequence elements in the absence of supercoiling. This analysis is based on the observation (Caserta et al. (1989) Nucleic Acids Res. 17, 8521-8532 and (1990) Biochemistry 29, 8152-8157) that the reaction of eukaryotic DNA topoisomerase I occurs on two types of DNA sites: sites S (Supercoiled induced) and sites C (Constitutive, whose presence is topology-independent). We report that sites C are abundant on the intrinsically curved DNAs analyzed. The DNAs studied were two intrinsically curved segments of different origin: the Crithidia fasciculata kinetoplast DNA and the bent-containing domain B of the Saccharomyces cerevisiae ARS1. On these DNA segments DNA topoisomerase I cleaves at the junctions between the poly(A) tracts and mixed-sequence DNA. Analysis of the conformation of the double helix around the cleavage sites has revealed that the reaction occurs in correspondence of a defined DNA conformational motif. This motif is described by the set of Eulerian angular values that define the axial path of DNA (helical twist, deflection angle, direction) and of the orthogonal components of wedge (roll and tilt).
对真核生物DNA拓扑异构酶I在两条固有弯曲DNA上组成性且优先切割的位点进行分析,揭示了在无超螺旋情况下,能引发在诱导弯曲的序列元件上发生切割反应的构象特征。该分析基于以下观察结果(卡塞塔等人(1989年)《核酸研究》17卷,8521 - 8532页以及(1990年)《生物化学》29卷,8152 - 8157页),即真核生物DNA拓扑异构酶I的反应发生在两类DNA位点上:S位点(超螺旋诱导位点)和C位点(组成性位点,其存在与拓扑结构无关)。我们报告在所分析的固有弯曲DNA上C位点丰富。所研究的DNA是两个不同来源的固有弯曲片段:纤细无脊鞭毛虫动质体DNA以及酿酒酵母ARS1的含弯曲结构域B。在这些DNA片段上,DNA拓扑异构酶I在聚(A)序列与混合序列DNA的连接处进行切割。对切割位点周围双螺旋构象的分析表明,反应发生在特定的DNA构象基序处。这个基序由定义DNA轴向路径(螺旋扭转、偏转角、方向)以及楔形正交分量(滚动和倾斜)的欧拉角值集合来描述。