Craigie R, Mizuuchi K
Cell. 1986 Jun 20;45(6):793-800. doi: 10.1016/0092-8674(86)90554-4.
DNA strand transfer at the initiation of Mu transposition normally requires a negatively supercoiled transposon donor molecule, containing both ends of Mu in inverted repeat orientation. We propose that the specific relative orientation of the Mu ends is needed only to energetically favor a particular configuration that the ends must adopt in a synaptic complex. The model was tested by constructing special donor DNA substrates that, because of their catenation or knotting, energetically favor this same configuration of the Mu ends, even though they are on separate molecules or in direct repeat orientation. These structures are efficient substrates for the strand transfer reaction, whereas appropriate control structures are not. The result eliminates tracking or protein scaffold models for orientation preference. Several other systems in which the relative orientation of two DNA segments is sensed may utilize the same mechanism.
在Mu转座起始时的DNA链转移通常需要一个负超螺旋转座子供体分子,该分子包含处于反向重复方向的Mu的两端。我们提出,Mu末端的特定相对方向仅在能量上有利于末端在突触复合体中必须采用的特定构象。通过构建特殊的供体DNA底物对该模型进行了测试,由于它们的连环或打结,即使Mu末端位于不同分子上或处于正向重复方向,在能量上也有利于这种相同的构象。这些结构是链转移反应的有效底物,而适当的对照结构则不是。该结果排除了用于方向偏好的追踪或蛋白质支架模型。其他几个可感知两个DNA片段相对方向的系统可能利用相同的机制。