Andrews B J, McLeod M, Broach J, Sadowski P D
Mol Cell Biol. 1986 Jul;6(7):2482-9. doi: 10.1128/mcb.6.7.2482-2489.1986.
The 2 micron plasmid of Saccharomyces cerevisiae codes for a site-specific recombinase, the FLP protein, that catalyzes efficient recombination across two 599-base-pair (bp) inverted repeats of the plasmid DNA both in vivo and in vitro. We analyzed the interaction of the purified FLP protein with the target sequences of two point mutants that exhibit impaired FLP-mediated recombination in vivo. One mutation lies in one of the 13-bp repeat elements that had been previously shown to be protected from DNase digestion by the FLP protein. This mutation dramatically reduces FLP-mediated recombination in vitro and appears to act by reducing the binding of FLP protein to its target sequence. The second mutation lies within the 8-bp core region of the FLP target sequence. The FLP protein introduces staggered nicks surrounding this 8-bp region, and these nicks are thought to define the sites of strand exchange. The mutation in the core region abolishes recombination with a wild-type site. However, recombination between two mutated sites is very efficient. This result suggests that proper base pairing between the two recombining sites is an important feature of FLP-mediated recombination.
酿酒酵母的2微米质粒编码一种位点特异性重组酶,即FLP蛋白,它在体内和体外都能催化质粒DNA的两个599碱基对(bp)反向重复序列之间的高效重组。我们分析了纯化的FLP蛋白与两个点突变体的靶序列之间的相互作用,这两个点突变体在体内表现出FLP介导的重组受损。一个突变位于13bp重复元件之一中,先前已证明该元件可被FLP蛋白保护免受DNase消化。这种突变在体外显著降低了FLP介导的重组,并且似乎是通过减少FLP蛋白与其靶序列的结合来起作用的。第二个突变位于FLP靶序列的8bp核心区域内。FLP蛋白在这个8bp区域周围引入交错切口,这些切口被认为定义了链交换的位点。核心区域的突变消除了与野生型位点的重组。然而,两个突变位点之间的重组非常高效。这一结果表明,两个重组位点之间正确的碱基配对是FLP介导的重组的一个重要特征。