Grogan D W, Cronan J E
Mol Gen Genet. 1984;196(2):367-72. doi: 10.1007/BF00328074.
The phenotypically silent cyclopropane fatty acid synthesis (cfa) gene of Escherichia coli K-12 has been located on the genetic linkage map. This was accomplished by integrating (via homologous recombination) the selectable marker of a recombinant plasmid into the host chromosome near the cfa locus. This integration allowed the subsequent isolation of a cfa-linked transposon Tn10 insertion. Genetic mapping of the Tn10 insertion, using conventional techniques, placed the cfa locus at min 36.5 on the linkage map in the vicinity of several other non-selectable markers. We ordered cfa and these other loci by three-factor transductional analyses. Selection for excision of the Tn10 element resulted in several types of mutants which harbor mutations of cfa and of neighboring genes, presumably as a consequence of Tn10-catalyzed chromosomal rearrangements.
大肠杆菌K-12中表型沉默的环丙烷脂肪酸合成(cfa)基因已定位在遗传连锁图上。这是通过(经由同源重组)将重组质粒的选择标记整合到宿主染色体上靠近cfa基因座的位置来实现的。这种整合使得随后能够分离出与cfa连锁的转座子Tn10插入。使用传统技术对Tn10插入进行遗传作图,将cfa基因座定位在连锁图上36.5分钟处,靠近其他几个非选择标记。我们通过三因子转导分析对cfa和其他这些基因座进行了排序。选择切除Tn10元件导致了几种类型的突变体,这些突变体含有cfa和邻近基因的突变,推测这是Tn10催化的染色体重排的结果。