Shen M M, Raleigh E A, Kleckner N
Genetics. 1987 Jul;116(3):359-69. doi: 10.1093/genetics/116.3.359.
We have investigated by Southern blot hybridization the rate of IS10 transposition and other Tn10/IS10-promoted rearrangements in Escherichia coli and Salmonella strains bearing single chromosomal insertions of Tn10 or a related Tn10 derivative. We present evidence for three primary conclusions. First, the rate of IS10 transposition is approximately 10(-4) per cell per bacterial generation when overnight cultures are grown and plated on minimal media and is at least ten times more frequent than any other Tn10/IS10-promoted DNA alteration. Second, all of the chromosomal rearrangements observed can be accounted for by two previously characterized Tn10-promoted rearrangements: deletion/inversions and deletions. Together these rearrangements occur at about 10% the rate of IS10 transposition. Third, the data suggest that intramolecular Tn10-promoted rearrangements preferentially use nearby target sites, while the target sites for IS10 transposition events are scattered randomly around the chromosome.
我们通过Southern印迹杂交研究了携带单个染色体插入Tn10或相关Tn10衍生物的大肠杆菌和沙门氏菌菌株中IS10转座率以及其他Tn10/IS10促进的重排情况。我们提供了三个主要结论的证据。第一,当过夜培养物在基本培养基上生长并铺板时,IS10转座率约为每细胞每细菌代10^(-4),且比任何其他Tn10/IS10促进的DNA改变至少频繁十倍。第二,观察到的所有染色体重排都可以由两种先前表征的Tn10促进的重排来解释:缺失/倒位和缺失。这些重排一起发生的频率约为IS10转座率的10%。第三,数据表明分子内Tn10促进的重排优先使用附近的靶位点,而IS10转座事件的靶位点则随机分布在染色体周围。