Kleckner N, Steele D A, Reichardt K, Botstein D
Genetics. 1979 Aug;92(4):1023-40. doi: 10.1093/genetics/92.4.1023.
Genetic analysis of 131 independent transpositions of the tetracycline-resistance element Tn10 from a single site in phage P22 into the histidine operon of Salmonella typhimurium reveals that Tn10 insertions are not randomly distributed along this chromosomal target. The insertions occur in 22 different "clusters"; insertions within each cluster are very tightly linked in recombination tests. Tn10 insertions are not evenly distributed among the identified clusters. The existence of these clusters suggests that this chromosomal target contains particular genetic signals that guide Tn10 to particular preferred positions for insertion. Insertions within each cluster occur in both orientations with roughly equal frequency.--The relationship among different insertions within each cluster has been examined. The resolution of genetic mapping places an upper limit of about 50 basepairs on the distance between different insertions within a cluster. Different insertions within a cluster usually have the same reversion frequency; however, heterogeneity in reversion frequency has been detected in at least two clusters. For most clusters, the available data are consistent with the simple possibility that all insertions within a cluster are at identical positions; however, the data do not exclude other possibilities.
对131个独立的四环素抗性元件Tn10从噬菌体P22的单个位点转座到鼠伤寒沙门氏菌组氨酸操纵子的遗传分析表明,Tn10插入在这个染色体靶标上并非随机分布。插入发生在22个不同的“簇”中;在重组试验中,每个簇内的插入紧密连锁。Tn10插入在已鉴定的簇中分布不均。这些簇的存在表明,这个染色体靶标含有特定的遗传信号,可引导Tn10插入到特定的优先位置。每个簇内的插入以大致相等的频率以两种方向发生。——已研究了每个簇内不同插入之间的关系。遗传图谱的分辨率对簇内不同插入之间的距离设定了约50个碱基对的上限。一个簇内的不同插入通常具有相同的回复频率;然而,至少在两个簇中检测到回复频率的异质性。对于大多数簇来说,现有数据与一个簇内所有插入都处于相同位置的简单可能性一致;然而,这些数据并不排除其他可能性。