Vergunst A C, Hooykaas P J
Institute of Molecular Plant Sciences, Leiden, The Netherlands.
Plant Mol Biol. 1998 Oct;38(3):393-406. doi: 10.1023/a:1006024500008.
The Cre/lox system was used to obtain targeted integration of an Agrobacterium T-DNA at a lox site in the genome of Arabidopsis thaliana. Site-specific recombinants, and not random events, were preferentially selected by activation of a silent lox-neomycin phosphotransferase (nptII) target gene. To analyse the effectiveness of Agrobacterium-mediated transfer we used T-DNA vectors harbouring a single lox sequence (this vector had to circularize at the T-DNA left- and right-border sequences prior to site-specific integration) or two lox sequences (this vector allowed circularization at the lox sequences within the T-DNA either prior to or after random integration, followed by targeting of the circularized vector), respectively. Furthermore, to control the reversibility of the integration reaction, Cre recombinase was provided transiently by using a cotransformation approach. One precise stable integrant was found amongst the recombinant calli obtained after transformation with a double-lox T-DNA vector. The results indicate that Agrobacterium-mediated transformation can be used as a tool to obtain site-specific integration.
利用Cre/lox系统在拟南芥基因组的lox位点实现农杆菌T-DNA的靶向整合。通过激活沉默的lox-新霉素磷酸转移酶(nptII)靶基因,优先选择位点特异性重组体而非随机事件。为了分析农杆菌介导转移的有效性,我们分别使用了携带单个lox序列的T-DNA载体(该载体在进行位点特异性整合之前必须在T-DNA左右边界序列处环化)或两个lox序列的T-DNA载体(该载体允许在随机整合之前或之后在T-DNA内的lox序列处环化,随后靶向环化载体)。此外,为了控制整合反应的可逆性,通过共转化方法瞬时提供Cre重组酶。在用双lox T-DNA载体转化后获得的重组愈伤组织中发现了一个精确的稳定整合体。结果表明,农杆菌介导的转化可作为获得位点特异性整合的工具。