Jung Ui-Jung, Park Sun, Lee Gwang, Shin Ho-Joon, Kwon Myung-Hee
Department of Microbiology, Ajou University School of Medicine, Woncheon-dong 5, Suwon 442-749, Republic of Korea.
Biochem Biophys Res Commun. 2007 Nov 9;363(1):183-9. doi: 10.1016/j.bbrc.2007.08.145. Epub 2007 Aug 30.
In Cre-loxP recombination system, Cre recombinase binds cooperatively to two 13bp inverted repeats in a 34bp loxP and catalyzes strand exchange in the 8bp spacer region. Up to date, spacer sequences within the recombined loxP sites derived from two loxP sties that have different 8bp spacer regions have never been analyzed. In the present study, we analyzed the spacer sequences within the recombined products, resulted from intramolecular recombination between heterologous loxP sites including M2, M3, M7, M11, and 2272 in vivo and in vitro. From the analyses, it was found that loxP sites with aberrant 8bp spacers can be generated from Cre-mediated recombination between heterologous loxP sites at significantly high frequency, proposing the possibility that recombination between heterologous loxP sites would have not undergone typical formula of Cre-loxP recombination.
在Cre-loxP重组系统中,Cre重组酶协同结合到34bp loxP中的两个13bp反向重复序列上,并催化8bp间隔区的链交换。到目前为止,源自具有不同8bp间隔区的两个loxP位点的重组loxP位点内的间隔序列从未被分析过。在本研究中,我们分析了体内和体外包括M2、M3、M7、M11和2272在内的异源loxP位点之间分子内重组产生的重组产物中的间隔序列。通过分析发现,具有异常8bp间隔的loxP位点可以通过异源loxP位点之间的Cre介导的重组以显著高的频率产生,这表明异源loxP位点之间的重组可能没有经历典型的Cre-loxP重组模式。