Rubens C, Heffron F, Falkow S
J Bacteriol. 1976 Oct;128(1):425-34. doi: 10.1128/jb.128.1.425-434.1976.
Insertion of the transposable deoxyribonucleic acid sequence that specifies the TEM beta-lactamase (TnA) occurred in at least 19 sites on the 5.5 x 10(6)-dalton plasmid RSF1010. There was no significant difference in the frequency of transposition or in the distribution of TnA insertion sites for recombinant plasmids isolated from recombination-proficient (rec+) or recombination-deficient (rec-) bacterial host cells. The site and orientation of TnA insertions were determined by both heteroduplex analysis and enzymatic digestion with restriction endonucleases. Insertion in the gene encoding for sulfonamide resistance occurred without circular permutation in one or the other of two distinct orientations. Insertions in orientation P were strongly polar on distal gene expression, whereas insertions in orientation M were mutagenic but not polar. In addition, we have observed that TnA elements from different R plasmids show fine structural heterogeneity, and that TnA insertion at a site adjacent to the origin of replication causes an increase in plasmid copy number.
编码TEMβ-内酰胺酶(TnA)的转座脱氧核糖核酸序列插入到了5.5×10⁶道尔顿的质粒RSF1010上至少19个位点。从重组能力正常(rec⁺)或重组缺陷(rec⁻)细菌宿主细胞中分离出的重组质粒,其转座频率或TnA插入位点的分布没有显著差异。通过异源双链分析和限制性内切酶酶切确定了TnA插入的位点和方向。在编码磺胺抗性的基因中插入时,会以两种不同方向中的一种或另一种发生,且没有环形排列。P方向的插入对远端基因表达具有强烈的极性作用,而M方向的插入具有诱变作用但无极性。此外,我们观察到来自不同R质粒的TnA元件显示出精细的结构异质性,并且在与复制起点相邻的位点插入TnA会导致质粒拷贝数增加。