Puyang Xiaoling, Lee Karen, Pawlichuk Corey, Kunimoto Dennis Y
Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Canada T6G 2H71.
Microbiology (Reading). 1999 Nov;145 ( Pt 11):3163-3168. doi: 10.1099/00221287-145-11-3163.
An insertion sequence designated IS1626 was isolated and characterized from a Mycobacterium avium clinical strain. IS1626 was detected by high-stringency hybridization with the pMB22/S12 probe from IS900 of Mycobacterium paratuberculosis. IS1626 is 1418 bp in size and has a G+C content of 65 mol%. It has neither terminal inverted repeats nor flanking direct repeats. Analysis of three IS1626 insertion sites in the M. avium strain and the corresponding potential insertion sites in two IS1626-free M. avium strains indicated a consensus sequence of CATGCN(4-5)TCCTN(2)G for IS1626 insertion. In the three clones examined, IS1626 has the same orientation with respect to this target site. IS1626 has two major ORFs. ORF1179 encodes a predicted protein of 393 amino acids. ORF930, on the complementary strand of ORF1179, encodes a protein of 310 amino acids. The Shine-Dalgarno sequence for ORF930 is partially located in the flanking region, similar to other IS900-related elements. Analysis of the comparable features of insertion sequences and their variable occurrence in related organisms is useful for studying the evolution of these elements and their hosts.
从一株鸟分枝杆菌临床菌株中分离并鉴定出一个名为IS1626的插入序列。通过与副结核分枝杆菌IS900的pMB22/S12探针进行高严谨度杂交检测到IS1626。IS1626大小为1418 bp,G+C含量为65 mol%。它既没有末端反向重复序列,也没有侧翼正向重复序列。对鸟分枝杆菌菌株中的三个IS1626插入位点以及两个无IS1626的鸟分枝杆菌菌株中的相应潜在插入位点进行分析,结果表明IS1626插入的共有序列为CATGCN(4 - 5)TCCTN(2)G。在所检测的三个克隆中,IS1626相对于该靶位点具有相同的方向。IS1626有两个主要的开放阅读框。ORF1179编码一个预测的由393个氨基酸组成的蛋白质。位于ORF1179互补链上的ORF930编码一个由310个氨基酸组成的蛋白质。ORF930的Shine-Dalgarno序列部分位于侧翼区域,这与其他IS900相关元件类似。分析插入序列的可比特征及其在相关生物体中的可变出现情况,对于研究这些元件及其宿主的进化是有用的。