Lodge J K, Berg D E
Department of Molecular Microbiology, Washington University Medical School, St. Louis, Missouri 63110.
J Bacteriol. 1990 Oct;172(10):5956-60. doi: 10.1128/jb.172.10.5956-5960.1990.
The major hot spot of transposon Tn5 insertion in plasmid pBR322 (hot spot I) is in the promoter for the tetracycline resistance gene (tet). We made a series of pBR322 derivatives with mutations in and around this promoter and assayed their effects on insertion of Tn5 into hot spot I. Those mutations which reduced transcription from the tet promoter also reduced the frequency of insertion into hot spot I. Transcription and translation of tet are thought to cause the formation of paired domains of negative and positive supercoiling in pBR322. An amber codon in tet, 345 base pairs from hot spot I, decreases the negative supercoiling of the DNA segment containing hot spot I because it terminates translation of tet prematurely. We report here that this amber mutation also reduces insertion into hot spot I. These results suggest that the ability of Tn5 to insert into its major hot spot in pBR322 depends directly on negative supercoiling of the target DNA.
转座子Tn5插入质粒pBR322的主要热点(热点I)位于四环素抗性基因(tet)的启动子区域。我们构建了一系列在该启动子及其周围具有突变的pBR322衍生物,并检测了它们对Tn5插入热点I的影响。那些降低tet启动子转录的突变也降低了插入热点I的频率。tet的转录和翻译被认为会导致pBR322中正负超螺旋配对结构域的形成。tet基因中距离热点I 345个碱基对处的一个琥珀密码子,由于它过早终止tet的翻译,从而降低了包含热点I的DNA片段的负超螺旋。我们在此报告,这种琥珀突变也会减少插入热点I的情况。这些结果表明,Tn5插入pBR322中其主要热点的能力直接取决于靶DNA的负超螺旋。