Dean F B, Stasiak A, Koller T, Cozzarelli N R
J Biol Chem. 1985 Apr 25;260(8):4975-83.
We investigated systematically the knotting of nicked circular duplex DNA by Escherichia coli topoisomerase I. Agarose gel electrophoresis of knots forms a ladder of DNA bands. Each rung is made up of a variety of knots with the same number of nodes, or segment crossings; knots in adjacent rungs differ by one node. We extended the technique of electron microscopy of recA protein-coated DNA to the visualization of the complex knots tied by topoisomerase I. The striking result is that the enzyme produces every knot theoretically possible. The requirement for excess enzyme to form complex knots suggests a role for topoisomerase I in contorting the DNA in addition to promoting strand passage. We conclude that nodes formed are equally likely to be positive or negative and that topoisomerase I can pass DNA strands through a transient enzyme-generated break without regard to orientation of the passing strand. The results are interpreted in terms of a formulation for the topological requirements for knotting.
我们系统地研究了大肠杆菌拓扑异构酶I对带切口的环状双链DNA的打结情况。对结进行琼脂糖凝胶电泳会形成一系列DNA条带。每一级由具有相同节点数或片段交叉数的多种结组成;相邻两级的结相差一个节点。我们将recA蛋白包被的DNA的电子显微镜技术扩展到对拓扑异构酶I所形成的复杂结的可视化。引人注目的结果是,该酶产生了理论上可能的每一种结。形成复杂结需要过量的酶,这表明拓扑异构酶I除了促进链通过外,在使DNA扭曲方面也发挥作用。我们得出结论,形成的节点正负性出现的可能性相同,并且拓扑异构酶I可以使DNA链通过由酶瞬时产生的断裂,而不考虑通过链的方向。根据打结的拓扑学要求的一种表述对结果进行了解释。