Tu C P, Cohen S N
Cell. 1980 Jan;19(1):151-60. doi: 10.1016/0092-8674(80)90396-7.
247 independent events involving insertion of the TN3 transposable element into a 4 kb constructed plasmid (pTU4) of partially known DNA sequence were studied by restriction endonuclease mapping, and 65 of these insertion sites were examined further by DNA sequence analysis. Our results show that the previously proposed regional specificity for Tn3 insertion is associated with a strong preference for AT-rich segments as insertion sites. Moreover, multiple insertions of the Tn3 occurred at certain AT-rich nucleotide positions, and 23 of 26 independent insertion events at a single nucleotide position were found to be in the same orientation. A region of the recipient plasmid showing major homology with the terminal 18 bp of Tn3 was identified in the vicinity of an 11 nucleotide segment that included three insertional hot spots and 36 independent insertions. Our results indicate that the site and orientation of insertion of Tn3 are at least partly determined by the primary nucleotide sequence of the recipient genome, and suggest that insertional hot spots may result from the combined effects of AT richness plus homology of the recipient genome with the terminal sequences of Tn3.
通过限制性内切酶图谱分析研究了247个独立事件,这些事件涉及将TN3转座元件插入部分已知DNA序列的4kb构建质粒(pTU4)中,并通过DNA序列分析进一步检查了其中65个插入位点。我们的结果表明,先前提出的Tn3插入区域特异性与对富含AT的片段作为插入位点的强烈偏好有关。此外,Tn3在某些富含AT的核苷酸位置发生多次插入,并且在单个核苷酸位置的26个独立插入事件中有23个被发现是同向的。在一个包含三个插入热点和36个独立插入的11个核苷酸片段附近,鉴定出了与Tn3末端18bp具有主要同源性的受体质粒区域。我们的结果表明,Tn3的插入位点和方向至少部分由受体基因组的一级核苷酸序列决定,并表明插入热点可能是由富含AT以及受体基因组与Tn3末端序列的同源性共同作用的结果。