Vasil'chenko L G, Mkrtumian N M, Lomovskaia N D
Genetika. 1981;17(11):1967-74.
Actinophage phi C31 deletion c mutants with impaired ability to make repressor were genetically studied. Genetic crosses indicate that the c28 deletion mutant is situated with the c-region of the phi C31 genetic map. Based on the results of a qualitive test for recombination between several c mutants, a scheme of their order relative to deletion mutants was presented. The approximate distances between eight c mutants have been represented in units of the physical DNA map estimation. Genetic studies of actinophage lyg deletion mutants which cannot lysogenize sensitive cultures were carried out. Mutants failed to lysogenize upon mixed infection with lyg+ phages. The absence of the effect of lyg+ gene in trans suggests that lyg deletions cause a structural defect in an integration site of the phage. Preliminary data on alignment of lyg positions on physical and genetic maps of phi C31 phage have been obtained. According to evidence from genetic crosses, lyg mutation has been located in the right half of the phi C31 genome.
对产生阻遏物能力受损的肌动噬菌体φC31缺失c突变体进行了遗传学研究。遗传杂交表明,c28缺失突变体位于φC31遗传图谱的c区域。基于几个c突变体之间重组的定性测试结果,给出了它们相对于缺失突变体的顺序方案。八个c突变体之间的近似距离已以物理DNA图谱估计单位表示。对不能使敏感培养物溶源化的肌动噬菌体lyg缺失突变体进行了遗传学研究。这些突变体在与lyg+噬菌体混合感染时不能溶源化。lyg+基因的反式效应缺失表明,lyg缺失导致噬菌体整合位点的结构缺陷。已获得关于φC31噬菌体物理图谱和遗传图谱上lyg位置排列的初步数据。根据遗传杂交的证据,lyg突变位于φC31基因组的右半部分。