Hopkins J D, Clements M B, Liang T Y, Isberg R R, Syvanen M
Proc Natl Acad Sci U S A. 1980 May;77(5):2814-8. doi: 10.1073/pnas.77.5.2814.
The Escherichia coli sex factor stimulates precise excision of transposons Tn5 and Tn10 from sites either within the bacterial chromosome or within the factor itself. We have isolated two kinds of mutations that affect this activity. The ferA mutations eliminate the stimulation; the ferB mutations enhance it in the presence of FerA+. We conclude that ferA defines a sex factor gene that stimulates precise excision. The ferB mutations also specifically increase the rate of recombination between two IS3 elements on F' lac-pro (F'128) in a reaction that requires the product of recA. The stimulation of this recombination by ferB also requires an active ferA gene, which implies that the ferA gene stimulates this reaction as well as precise excision. A ferA mutation was mapped at 84.2 kilobases on the F factor, and a ferB mutation was mapped at 82.5 kilobases. The fer mutants were obtained by an approach that permits the isolation of mutants affecting precise excision.
大肠杆菌性因子可刺激转座子Tn5和Tn10从细菌染色体内部位点或因子自身内部位点精确切除。我们分离出了两种影响该活性的突变。ferA突变消除了这种刺激作用;ferB突变在存在FerA+的情况下增强了这种刺激作用。我们得出结论,ferA定义了一个刺激精确切除的性因子基因。ferB突变还在需要recA产物的反应中特异性地提高了F'lac-pro(F'128)上两个IS3元件之间的重组率。ferB对这种重组的刺激也需要一个活性ferA基因,这意味着ferA基因既刺激这种反应也刺激精确切除。一个ferA突变定位在F因子上84.2千碱基处,一个ferB突变定位在82.5千碱基处。fer突变体是通过一种允许分离影响精确切除的突变体的方法获得的。