Brown A M, Coupland G M, Willetts N S
J Bacteriol. 1984 Aug;159(2):472-81. doi: 10.1128/jb.159.2.472-481.1984.
The IncN plasmids R46 and N3 each contain two copies of an insertion sequence which we denote IS46. This insertion sequence has single PstI and SalI restriction sites and is 0.81 kilobases long. All four copies of IS46 were capable of forming cointegrates, although the DNA between the insertion sequences, which in each case carries a tetracycline resistance gene, was not transposable in the form of a compound transposon. IS46-mediated cointegrates resolved in Rec+ but not in RecA- cells. Recombination between two copies of IS46, causing an inversion, accounts for the existence of two distinct forms of R46. IS46-mediated deletions were probably responsible for the formation of the plasmid pKM101 from R46. IS46 was not homologous to IS1 but did show homology with IS15.
IncN质粒R46和N3各自含有我们称为IS46的插入序列的两个拷贝。这个插入序列有单个PstI和SalI限制酶切位点,长度为0.81千碱基。IS46的所有四个拷贝都能够形成共整合体,尽管插入序列之间的DNA(在每种情况下都携带四环素抗性基因)不能以复合转座子的形式转座。IS46介导的共整合体在Rec⁺细胞中解离,但在RecA⁻细胞中不解离。两个IS46拷贝之间的重组导致倒位,这解释了R46存在两种不同形式的原因。IS46介导的缺失可能是质粒pKM101从R46形成的原因。IS46与IS1不同源,但与IS15显示出同源性。