Naito A, Naito S, Ikeda H
Mol Gen Genet. 1984;193(2):238-43. doi: 10.1007/BF00330674.
We have previously shown that DNA gyrase of Escherichia coli can promote recombination between heterologous DNAs in a cell-free system (Ikeda et al. 1982). In the present paper, we have studied the nucleotide sequences of several recombination junctions of lambda-pBR322 recombinants and found that there were not more than three-basepair homologies between the parental DNAs in six combinations of the lambda and pBR322 recombination sites. Based on this and previous results, we concluded that homology was not required for the DNA gyrase-mediated recombination. Furthermore, the structures of the recombinant DNAs we have analyzed suggest the occurrence of multiple cross-overs in our in vitro system.
我们之前已经表明,大肠杆菌的DNA促旋酶可以在无细胞系统中促进异源DNA之间的重组(池田等人,1982年)。在本文中,我们研究了λ-pBR322重组体几个重组连接点的核苷酸序列,发现在λ和pBR322重组位点的六种组合中,亲本DNA之间的同源性不超过三个碱基对。基于此及之前的结果,我们得出结论,DNA促旋酶介导的重组不需要同源性。此外,我们分析的重组DNA的结构表明在我们的体外系统中发生了多次交叉。