Tenzen T, Matsutani S, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
J Bacteriol. 1990 Jul;172(7):3830-6. doi: 10.1128/jb.172.7.3830-3836.1990.
IS630 is a 1.15-kilobase sequence in Shigella sonnei that, unlike many mobile elements, seems not to mediate cointegration between different replicons. To assess its transposition, we constructed composite elements containing inverted copies of IS630 flanking a drug resistance gene. We found that these composite elements transposed to plasmid ColE1 in Escherichia coli. DNA sequencing showed that transposition was, in all cases, to the dinucleotide sequence 5'-TA-3'. There were two preferred insertion sites which corresponded to the TA sequences in the inverted repeats of a 13-base-pair stem region of the [rho]-dependent transcription terminator. IS630 is flanked by TA, and nucleotide substitution by in vitro mutagenesis at these ends did not affect transposition activity of a composite element or its ability to insert preferentially into TA within the 13-base-pair inverted repeat sequences or to duplicate the target sequence.
IS630是宋内志贺氏菌中的一段1.15千碱基序列,与许多移动元件不同,它似乎不介导不同复制子之间的共整合。为了评估其转座情况,我们构建了复合元件,这些元件含有位于耐药基因两侧的IS630反向拷贝。我们发现这些复合元件可转座至大肠杆菌中的质粒ColE1。DNA测序表明,在所有情况下,转座均发生在二核苷酸序列5'-TA-3'处。存在两个优先插入位点,它们对应于依赖ρ因子的转录终止子13碱基对茎区反向重复序列中的TA序列。IS630两侧为TA,通过体外诱变对这些末端进行核苷酸取代并不影响复合元件的转座活性,也不影响其优先插入13碱基对反向重复序列内TA的能力或复制靶序列的能力。