Sherratt D J, Dougan G, Saul M, Sunar B, Twigg A, Warren G
Contrib Microbiol Immunol. 1979;6:100-10.
Analysis of plasmid ColE1, its naturally occurring relatives ColK and CloDF13, and a wide range of ColE1 derivatives containing either insertions or deletions of genetic material has allowed localization on the ColE1 genome of DNA sequences responsible for colicin E1 synthesis, immunity to colicin killing, conjugal mobility and incompatibility. We have examined incompatibility between pairs of ColE1 derivatives ranging in size from 2.6 to 13.8 Md. Though all the plasmids tested exerted ColE1 incompatibility, a definite pattern was observed regarding the dominant plasmid in any pair tested (i.e. the plasmid that displaces the other from a heterozygote). Usually the larger plasmid is displaced. We conclude that loci for incompatibility reside within 0.7 kb of the ColE1 replication region. A model is presented to explain both the incompatibility data and the observation that the fraction of total DNA occurring as ColE1-like plasmid in a cell is approximately constant. Transposons Tn1 and Tn3 (3.2 Md; Apr and approximately 85% homologous), Tn501 (5.5 Md; Hgr), and Tn7 (9.3 Md; Tpr Smr) can all be transposed into ColE1. Though all have closely related. Tn501 and Tn7 do not complement transposition of Tn3 transposition defective deletions. A Tn3-specified 19,000 dalton protein is absent in one particular class of transposition-defective deletion.
对质粒ColE1、其天然存在的亲缘质粒ColK和CloDF13,以及一系列含有遗传物质插入或缺失的ColE1衍生物进行分析,已确定了ColE1基因组上负责大肠杆菌素E1合成、对大肠杆菌素杀伤的免疫性、接合转移和不相容性的DNA序列的定位。我们研究了大小在2.6至13.8兆道尔顿之间的ColE1衍生物对之间的不相容性。尽管所有测试的质粒都表现出ColE1不相容性,但在任何测试对中(即从杂合子中取代另一个质粒的质粒)关于优势质粒观察到了明确的模式。通常较大的质粒被取代。我们得出结论,不相容性位点位于ColE1复制区域的0.7千碱基内。提出了一个模型来解释不相容性数据以及细胞中作为ColE1样质粒存在的总DNA比例大致恒定这一观察结果。转座子Tn1和Tn3(3.2兆道尔顿;Apr且约85%同源)、Tn501(5.5兆道尔顿;Hgr)和Tn7(9.3兆道尔顿;Tpr Smr)都可以转座到ColE1中。尽管它们都密切相关,但Tn501和Tn7不能互补Tn3转座缺陷缺失的转座。在一类特定的转座缺陷缺失中不存在Tn3指定的19,000道尔顿蛋白质。