Kmiec E B, Holloman W K
Cell. 1986 Feb 28;44(4):545-54. doi: 10.1016/0092-8674(86)90264-3.
Plasmids containing Z-DNA stretches can be paired and linked by combined action of Ustilago rec1 protein and topoisomerase. The product formed is a hemicatenated dimer in which two DNA rings are topologically intertwined at a region of homology. Superhelicity governs the reaction. Formation of linked product is coupled with formation of Z-DNA in the plasmid, a process dependent on the superhelix density. Pairing appears to initiate within the Z-DNA sequence, not at the unwound B-Z junction. The reaction can be blocked by a Z-DNA-specific binding protein, namely Z-DNA antibody. Plasmids with alternating Z-DNA dG-dC sequences at different sites on otherwise homologous molecules can be linked at the dG-dC sequences. However, a plasmid with a (dG-dC)n.(dG-dC)n Z-DNA stretch cannot be linked with a plasmid containing a (dG-dT)n.(dC-dA)n Z-DNA stretch.
含有Z-DNA片段的质粒可通过黑粉菌rec1蛋白和拓扑异构酶的联合作用进行配对和连接。形成的产物是一种半连环体二聚体,其中两个DNA环在同源区域发生拓扑缠绕。超螺旋性控制该反应。连接产物的形成与质粒中Z-DNA的形成相关联,这一过程依赖于超螺旋密度。配对似乎在Z-DNA序列内起始,而非在解旋的B-Z交界处。该反应可被一种Z-DNA特异性结合蛋白,即Z-DNA抗体阻断。在其他方面同源的分子上不同位点具有交替Z-DNA dG-dC序列的质粒可在dG-dC序列处连接。然而,具有(dG-dC)n.(dG-dC)n Z-DNA片段的质粒不能与含有(dG-dT)n.(dC-dA)n Z-DNA片段的质粒连接。