Jones M, Wagner R, Radman M
Cell. 1987 Aug 14;50(4):621-6. doi: 10.1016/0092-8674(87)90035-3.
The involvement of the E. coli methyl-directed and very short patch (vsp) mismatch repair systems in bacteriophage lambda recombination has been studied. Genetic crosses and heteroduplex transfection experiments were performed using lambda phages with sequenced mutations in the cl gene. The results indicate that methyl-directed repair does operate during bacteriophage lambda recombination but generally does not contribute to the formation of recombinants involving close markers. Vsp repair apparently acts during bacteriophage lambda recombination to produce recombinants involving close markers because its action does not involve extensive excision tracts. Marker-specific hyperrecombination and the apparent clustering of genetic exchanges in bacteriophage lambda recombination can be accounted for by the action of the vsp repair system.
对大肠杆菌甲基导向和极短片段(vsp)错配修复系统参与噬菌体λ重组进行了研究。使用在cl基因中有测序突变的λ噬菌体进行了遗传杂交和异源双链转染实验。结果表明,甲基导向修复在噬菌体λ重组过程中确实起作用,但通常对涉及紧密标记的重组体形成没有贡献。vsp修复显然在噬菌体λ重组过程中起作用,以产生涉及紧密标记的重组体,因为其作用不涉及广泛的切除片段。噬菌体λ重组中标记特异性的超重组和遗传交换的明显聚集可以通过vsp修复系统的作用来解释。