Kanaar R, van de Putte P, Cozzarelli N R
Department of Biochemistry, State University of Leiden, The Netherlands.
Proc Natl Acad Sci U S A. 1988 Feb;85(3):752-6. doi: 10.1073/pnas.85.3.752.
Inversion of the G loop of bacteriophage Mu requires the phage-encoded Gin protein and a host factor. The topological changes in a supercoiled DNA substrate generated by the two purified proteins were analyzed. More than 99% of the inversion products were unknotted rings. This result excludes synapsis by way of a random collision of recombination sites, because the resulting entrapped supercoils would be converted into knots by recombination. Instead, the recombination sites must come together in the synaptic complex in an ordered fashion with a fixed number of supercoils between the sites. The linking number of the substrate DNA increases by four during recombination. Thus, in three successive rounds of inversion, the change in linking number was +4, +8, and +12, respectively. These results lead to a quantitative model for the mechanism of Gin recombination that includes the distribution of supercoils in the synaptic complex, their alteration by strand exchange, and specific roles for the two proteins needed for recombination.
噬菌体Mu的G环倒位需要噬菌体编码的Gin蛋白和一个宿主因子。分析了由这两种纯化蛋白产生的超螺旋DNA底物中的拓扑变化。超过99%的倒位产物是无纽结环。该结果排除了通过重组位点随机碰撞进行联会的可能性,因为由此产生的被困超螺旋会通过重组转化为纽结。相反,重组位点必须以有序的方式在突触复合体中聚集在一起,位点之间有固定数量的超螺旋。在重组过程中,底物DNA的连接数增加4。因此,在连续三轮倒位中,连接数的变化分别为+4、+8和+12。这些结果得出了一个关于Gin重组机制的定量模型,该模型包括突触复合体中超螺旋的分布、它们通过链交换的改变以及重组所需的两种蛋白质的特定作用。