Karlovský P, Vasková M
Plasmid. 1986 Nov;16(3):219-21. doi: 10.1016/0147-619x(86)90060-0.
Insertions of Tn1000 into a cloned fragment of the L-phage genome comprising the repressor gene were prepared. Repressor activities produced by plasmids with insertions were assayed in vivo. As a result, the repressor gene was localized within 0.5 kb near one end of the cloned fragment. Transposon insertions were nonrandomly clustered within the repressor gene and in its close vicinity. An analysis of supercoiled plasmid DNA with the nuclease S1 revealed no distortion of the secondary structure of DNA in this region.
制备了Tn1000插入包含阻遏物基因的L噬菌体基因组克隆片段的产物。对带有插入片段的质粒在体内产生的阻遏物活性进行了测定。结果,阻遏物基因定位于克隆片段一端附近0.5 kb范围内。转座子插入在阻遏物基因及其紧邻区域内呈非随机聚集。用核酸酶S1分析超螺旋质粒DNA表明该区域DNA的二级结构未发生扭曲。