Aleixandre V, Blanco M
Instituto de Investigaciones Citológicas de la Caja de Ahorros de Valencia, Spain.
Mol Gen Genet. 1987 Aug;209(1):56-60. doi: 10.1007/BF00329836.
Cloning of an EcoRI restriction fragment, containing the 900 bp gamma-terminal sequence of transposon Tn1000, into pBR322, resulted in two plasmids, pICV63 and pICV64, which differed in the orientation of the cloned fragment within the replicon and in the level of ampicillin resistance conferred on the host cell. The DNAs of these plasmids differ in superhelicity and we suggest that a change in supercoiling of pICV63 DNA leads to this plasmid conferring resistance to only low levels of ampicillin, probably by reducing the expression of the bla gene. This hypothesis is supported by the fact that topA or supX mutations, which abolish topoisomerase I, reduce still further the level of resistance to ampicillin of pICV63-containing cells, whereas the gyrB226 compensatory mutation renders these cells more ampicillin resistant. Plasmid pICV63, therefore, enables mutant alleles of genes governing DNA topology to be recognized.
将一个含有转座子Tn1000 900 bpγ末端序列的EcoRI限制片段克隆到pBR322中,得到了两个质粒,pICV63和pICV64,它们在复制子内克隆片段的方向以及赋予宿主细胞的氨苄青霉素抗性水平上有所不同。这些质粒的DNA在超螺旋状态上存在差异,我们认为pICV63 DNA超螺旋状态的改变导致该质粒仅对低水平的氨苄青霉素具有抗性,这可能是通过降低bla基因的表达实现的。这一假设得到以下事实的支持:topA或supX突变会消除拓扑异构酶I,进一步降低含pICV63细胞对氨苄青霉素的抗性水平,而gyrB226补偿性突变则使这些细胞对氨苄青霉素更具抗性。因此,质粒pICV63能够识别控制DNA拓扑结构的基因突变等位体。