Lo Ta-Chun, Chen Hung-Wen, Tsai Yu-Kuo, Kuo Yang-Cheng, Lin Chao-Fen, Kuo Ssu-Ying, Lin Thy-Hou
Institute of Molecular Medicine and Department of Life Science, National Tsing Hua University, Hsinchu, Taiwan, ROC.
Microbiology (Reading). 2008 Apr;154(Pt 4):1047-1058. doi: 10.1099/mic.0.2007/013227-0.
An insertion sequence, ISLC3, of 1351 bp has been isolated from Lactobacillus casei. Formation of IS circles containing a 3 bp spacer (complete junction) or deletion of 25 bp at the left inverted repeat (IRL) between the abutted IS ends of the ISLC3 junction region (deleted junction) was also discovered in the lactobacilli and Escherichia coli system studied. We found that the promoter formed by the complete junction P(jun) was more active than that formed by the 25 bp deleted junction P(djun) or the indigenous promoter P(IRL). The corresponding transcription start sites for both promoter P(jun) and P(IRL) as well as P(djun) were subsequently determined using a primer extension assay. The activity of transposase OrfAB of ISLC3 was also assayed using an in vitro system. It was found that this transposase preferred to cleave a single DNA strand at the IRR over the IRL end in the transposition process, suggesting that attack of one end by the other was oriented from IRR to IRL.
