Shaw S Y, Wang J C
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 92138, USA.
Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):1692-7. doi: 10.1073/pnas.94.5.1692.
We show that supercoiling of a DNA trefoil, the simplest knotted ring, perturbs differently the spatial writhe of its two chiral forms. As a consequence, the negative-noded and positive-noded DNA trefoils can be resolved by gel electrophoresis. Analysis of the chirality of trefoils produced by cyclization of two linear DNAs demonstrates that the two chiral trefoils are produced in equal amounts, suggesting that these DNAs do not prefer intrinsic writhe of one chirality or the other. In contrast, knotting of nicked DNA rings by a molar excess of Saccharomyces cerevisiae DNA topoisomerase II produces more negative-noded than positive-noded trefoils, indicating an asymmetry in the interaction between the enzyme and DNA crossovers of different signs. These results suggest that asymmetry in DNA crossovers and intrinsic or ligand-induced writhe in a DNA might be detectable from an analysis of trefoil chirality.
我们表明,最简单的纽结环——DNA三叶结的超螺旋对其两种手性形式的空间扭曲有不同的扰动。因此,负节点和正节点的DNA三叶结可通过凝胶电泳分离。对由两条线性DNA环化产生的三叶结手性分析表明,两种手性三叶结的产生量相等,这表明这些DNA对一种或另一种手性的固有扭曲没有偏好。相比之下,用过量的酿酒酵母DNA拓扑异构酶II对带切口的DNA环进行纽结,产生的负节点三叶结比正节点三叶结更多,这表明该酶与不同符号的DNA交叉之间的相互作用存在不对称性。这些结果表明,DNA交叉的不对称性以及DNA中固有或配体诱导的扭曲可能可通过对三叶结手性的分析检测到。