Hernandez Perez M, Fomukong N G, Hellyer T, Brown I N, Dale J W
School of Biological Sciences, University of Surrey, Guildford, UK.
Mol Microbiol. 1994 Jun;12(5):717-24. doi: 10.1111/j.1365-2958.1994.tb01059.x.
A highly mobile insertion sequence designated IS1110 was detected in Mycobacterium avium strain LR541 following an observed increase in size of the plasmid pLR20. Genomic libraries of M. avium strains carrying either parental pLR20 or the modified plasmid (pLR20') were constructed and the sequence of the relevant clones was determined to characterize the insertion sequence and the target region. IS1110 is a 1457 bp element lacking terminal inverted repeats, and is related to IS900 (from Mycobacterium paratuberculosis), IS901 and IS902 (from M. avium) and to IS116 (from Streptomyces clavuligerus). LR541 carries several copies of IS1110. Individual colonies from the same plate show differences in Southern blot patterns when tested with an IS1110-derived probe; the ability to detect transposition events in random colonies, without any selection pressure, indicates an exceptionally high degree of mobility, which will be invaluable for transposon mutagenesis. Analyses of M. avium isolates from human, veterinary, and environmental sources showed that IS1110-hybridizing sequences are present in some M. avium isolates but they were not detected in strains of other mycobacterial species. The polymorphism exhibited in M. avium isolates suggests that this element may be useful for molecular epidemiological studies of M. avium infections.
在观察到鸟分枝杆菌菌株LR541的质粒pLR20大小增加后,检测到一种高度可移动的插入序列,命名为IS1110。构建了携带亲本pLR20或修饰质粒(pLR20')的鸟分枝杆菌菌株的基因组文库,并测定了相关克隆的序列,以表征插入序列和靶区域。IS1110是一个1457 bp的元件,缺乏末端反向重复序列,与IS900(来自副结核分枝杆菌)、IS901和IS902(来自鸟分枝杆菌)以及IS116(来自克拉维链霉菌)相关。LR541携带多个IS1110拷贝。当用源自IS1110的探针进行检测时,同一平板上的单个菌落显示出Southern杂交图谱的差异;在没有任何选择压力的情况下,能够在随机菌落中检测到转座事件,表明其具有极高的移动性,这对于转座子诱变将是非常宝贵的。对来自人类、兽医和环境来源的鸟分枝杆菌分离株的分析表明,一些鸟分枝杆菌分离株中存在与IS1110杂交的序列,但在其他分枝杆菌物种的菌株中未检测到。鸟分枝杆菌分离株中表现出的多态性表明,该元件可能有助于鸟分枝杆菌感染的分子流行病学研究。