Sakanian V A, Iakubov I Z, Alikhanian S I, Stepanov A I
Genetika. 1978 May;14(5):853-66.
Heteroduplex analysis of deletion mutants of plasmid pAS8 permitted to construct a physical map and to elaborate in greater detail the genetic map of RP4 plasmid. The correlation between the ability of mutants to replicate in cells lacking functional DNA-polymerase I and the length of the deleted segment permitted to map rep genes of RP4 on DNA region with coordinates 9.8-17.3 kb. A relationship between the manifestation of incompatibility of mutants with IncP-1 plasmids and the length of deletions indicates that inc genes(s) are located on DNA region with coordinates 2.1-9.8 kb. The analysis of replication of deletion mutants and the manifestation of incompatibility just as of the data about the size of appropriate deletions permitted to make the conclusion about the functional and genetic non-identity of the replication control and incompatibility control in RP4 plasmid. Different degrees of incompatibility manifested by different plasmids suggest a possible polygenic control of the incompatibility.
对质粒pAS8缺失突变体进行异源双链分析,有助于构建物理图谱,并更详细地阐述RP4质粒的遗传图谱。突变体在缺乏功能性DNA聚合酶I的细胞中复制的能力与缺失片段的长度之间的相关性,使得能够将RP4的rep基因定位在坐标为9.8 - 17.3 kb的DNA区域上。突变体与IncP - 1质粒不相容性的表现与缺失长度之间的关系表明,inc基因位于坐标为2.1 - 9.8 kb的DNA区域上。对缺失突变体复制情况以及不相容性表现的分析,正如关于适当缺失大小的数据一样,使得能够得出关于RP4质粒中复制控制和不相容性控制在功能和遗传上不相同的结论。不同质粒表现出的不同程度的不相容性表明,不相容性可能受到多基因控制。