Laboratory of Molecular Genetics, Institute of Medical Science, University of Tokyo, Shirokanedai, Minato-ku, Japan.
Genes Cells. 2011 Jul;16(7):765-77. doi: 10.1111/j.1365-2443.2011.01526.x.
Cre and FLP recombinases mediate not only specific deletions and insertions, but also the recombinase-mediated cassette exchange (RMCE) reaction, which is used in cell biotechnology including ES cells and mouse genetics. However, comparison of efficiencies for Cre and FLP in RMCE has not been made. We here examined the detailed process of RMCE with Cre and FLP in vitro using mutant loxP 2272 and three mutant FRTs (FRT G, FRT H, and FRT F3) and then quantitatively compared the RMCE reactions in vitro. Interestingly, in the in vitro reactions, the RMCE efficiency of Cre reached a plateau level of approximately 5% and did not proceed further, whereas that of FLPe reached approximately 12-13%, showing that FLPe reached a higher level of efficiency than Cre possibly when they were supplied at a very high concentration. Moreover, we quantitatively compared the production efficiency of E1-deleted adenovirus vector using the RMCE method with Cre or FLP. The results showed that FLPe was again found more efficient than Cre in RMCE reaction. Thus, although Cre is considered more active than, or similar to, FLPe, it may not be necessarily true for RMCE reaction. Possible reasons explaining these results are discussed.
Cre 和 FLP 重组酶不仅介导特异性缺失和插入,还介导重组酶介导的盒交换 (RMCE) 反应,该反应用于包括 ES 细胞和小鼠遗传学在内的细胞生物技术。然而,Cre 和 FLP 在 RMCE 中的效率比较尚未进行。我们在这里使用突变的 loxP 2272 和三个突变的 FRT(FRT G、FRT H 和 FRT F3)在体外检查了 Cre 和 FLP 的 RMCE 详细过程,然后定量比较了体外的 RMCE 反应。有趣的是,在体外反应中,Cre 的 RMCE 效率达到了约 5%的平台水平,不再进一步提高,而 FLPe 的效率达到了约 12-13%,表明当它们以非常高的浓度供应时,FLPe 达到了比 Cre 更高的效率水平。此外,我们使用 Cre 或 FLP 通过 RMCE 方法定量比较了 E1 缺失的腺病毒载体的生产效率。结果表明,在 RMCE 反应中,FLPe 再次比 Cre 更有效。因此,尽管 Cre 被认为比 FLPe 更活跃或与其相似,但对于 RMCE 反应可能并非如此。讨论了解释这些结果的可能原因。