Elliott T, Roth J R
Department of Biology, University of Utah, Salt Lake City 84112.
Mol Gen Genet. 1988 Aug;213(2-3):332-8. doi: 10.1007/BF00339599.
We have constructed a small, transposition-defective derivative of the transposon Tn10 that carries the chloramphenicol acetyltransferase gene of pACYC184. This new genetic element, Tn10d-Cam, transposes when Tn10 transposase is provided from a multi-copy plasmid. Transposon insertion mutagenesis of Salmonella typhimurium was performed by using a strain carrying a Tn10d-Cam insertion in an Escherichia coli F' episome as the donor in transductional crosses into recipients that carried a plasmid expressing Tn10 transposase. Tn10d-Cam insertion mutations were also generated by complementation in cis of Tn10d-Cam by a cotransducible Tn10 element that overproduces transposase. Here, transposase was provided only transiently, and the Tn10d-Cam insertion mutations were recovered in a transposase-free strain. Cis complementation was used for mutagenesis of a plasmid target. The site specificity of insertion and the effect of insertions on expression of a downstream gene were investigated, using Tn10d-Cam insertions in a plasmid carrying a segment of the histidine operon.
我们构建了转座子Tn10的一个小型、转座缺陷型衍生物,它携带pACYC184的氯霉素乙酰转移酶基因。这个新的遗传元件Tn10d-Cam,当从多拷贝质粒提供Tn10转座酶时会发生转座。鼠伤寒沙门氏菌的转座子插入诱变是通过使用一个在大肠杆菌F'附加体中携带Tn10d-Cam插入的菌株作为供体,在转导杂交中导入携带表达Tn10转座酶质粒的受体来进行的。Tn10d-Cam插入突变也通过一个共转导的过量产生转座酶的Tn10元件对Tn10d-Cam的顺式互补产生。在这里,转座酶仅短暂提供,并且在无转座酶的菌株中回收Tn10d-Cam插入突变。顺式互补用于质粒靶标的诱变。利用携带组氨酸操纵子片段的质粒中的Tn10d-Cam插入,研究了插入的位点特异性以及插入对下游基因表达的影响。