Makin G J, Szybalski W, Blattner F R
Genetics. 1982 Nov;102(3):299-317. doi: 10.1093/genetics/102.3.299.
Experiments have been performed to help clarify the role of nonhomologies in phage lambda recombination. Three-factor crosses were carried out, and the frequencies of single and double recombinants in the two adjoining intervals were compared when the central marker was either a double point mutation (v1v3) or deletion (rex-cI deletion) or nonhomologous substitution (imm434). In all cases the lefthand marker was a bio substitution (Fec- phenotype, which does not permit plating on recA-), and the righthand marker was an amber mutation in gene O. Experiments were performed in all four possible arrangements of the central and rightward markers, while selecting for the Fec+ phenotype on the recA- host. As anticipated, high negative interference (HNI) was observed with point mutations, but when the central marker was a substitution nonhomology, HNI was reduced about tenfold. Surprisingly, when the central marker was a simple deletion, a dramatic asymmetry in results was observed, with HNI being exhibited only when the central deletion marker was acquired by the double recombinant. These results indicate that under normal conditions (red+, gam+, rec+) and with noninhibited DNA replication, recombination in coliphage lambda entails a highly asymmetric step that could be at the level of strand transfer or mismatch repair.
已开展实验以帮助阐明噬菌体λ重组中非同源性的作用。进行了三因子杂交,当中心标记为双点突变(v1v3)、缺失(rex - cI缺失)或非同源替换(imm434)时,比较了两个相邻区间中单重组体和双重组体的频率。在所有情况下,左侧标记为生物替换(Fec - 表型,不允许在recA - 上平板培养),右侧标记为基因O中的琥珀突变。在中心和右侧标记的所有四种可能排列中进行了实验,同时在recA - 宿主上选择Fec + 表型。正如预期的那样,点突变观察到高负干扰(HNI),但当中心标记为替换非同源性时,HNI降低了约十倍。令人惊讶的是,当中心标记为简单缺失时,观察到结果存在显著不对称,仅当双重组体获得中心缺失标记时才表现出HNI。这些结果表明,在正常条件下(red + 、gam + 、rec + )且DNA复制未受抑制时,大肠杆菌噬菌体λ中的重组需要一个高度不对称的步骤,该步骤可能发生在链转移或错配修复水平。