Benson F, Collier S, Lloyd R G
Genetics Department, University of Nottingham, Queens Medical Centre, UK.
Mol Gen Genet. 1991 Feb;225(2):266-72. doi: 10.1007/BF00269858.
Genetic recombination in Escherichia coli was investigated by measuring the effect of mutations in ruv and rec genes on F-prime transfer and mobilization of nonconjugative plasmids. Mutation of ruv was found to reduce the recovery of F-prime transconjugants in crosses with recB recC sbcA strains by about 30-fold and with recB recC sbcB sbcC strains by more than 300-fold. Conjugative plasmids lacking any significant homology with the chromosome were transferred normally to these ruv mutants. Mobilization of the plasmid cloning vectors pHSG415, pBR322, pACYC184 and pUC18 were reduced by 20- to 100-fold in crosses with ruv rec+ sbc+ strains, depending on the plasmid used. Recombinant plasmids carrying ruv+ were transferred efficiently. With both F-prime transfer and F-prime cointegrate mobilization, the effect of ruv was suppressed by inactivating recA. It is proposed that the failure to recover transconjugants in ruv recA+ strains is due to abortive recombination and that the ruv genes define activities which function late in recombination to help convert recombination intermediates into viable products.
通过测量ruv和rec基因的突变对F'转移以及非接合性质粒的动员作用,研究了大肠杆菌中的基因重组。发现ruv突变会使与recB recC sbcA菌株杂交时F'转导子的回收率降低约30倍,与recB recC sbcB sbcC菌株杂交时降低超过300倍。与染色体缺乏任何显著同源性的接合性质粒可正常转移至这些ruv突变体。在与ruv rec+ sbc+菌株杂交时,质粒克隆载体pHSG415、pBR322、pACYC184和pUC18的动员能力降低了20至100倍,具体取决于所使用的质粒。携带ruv+的重组质粒可有效转移。在F'转移和F'共整合体动员中,ruv的作用均可通过使recA失活而得到抑制。有人提出,在ruv recA+菌株中未能回收转导子是由于流产重组,并且ruv基因定义了在重组后期发挥作用以帮助将重组中间体转化为有活力产物的活性。