Dymecki S M
Department of Embryology, Carnegie Institution of Washington, Baltimore, MD 21210, USA.
Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):6191-6. doi: 10.1073/pnas.93.12.6191.
Site-specific recombinases are being developed as tools for "in vivo" genetic engineering because they can catalyze precise excisions, integrations, inversions, or translocations of DNA between their distinct recognition target sites. Here it is demonstrated that Flp recombinase can effectively mediate site-specific excisional recombination in mouse embryonic stem cells, in differentiating embryonal carcinoma cells, and in transgenic mice. Broad Flp expression is compatible with normal development, suggesting that Flp can be used to catalyze recombination in most cell types. These properties indicate that Flp can be exploited to make prescribed alterations in the mouse genome.
位点特异性重组酶正被开发用作“体内”基因工程的工具,因为它们能够催化DNA在其不同的识别靶位点之间进行精确的切除、整合、倒位或易位。本文证明,Flp重组酶能在小鼠胚胎干细胞、分化中的胚胎癌细胞和转基因小鼠中有效介导位点特异性切除重组。广泛的Flp表达与正常发育兼容,这表明Flp可用于在大多数细胞类型中催化重组。这些特性表明,Flp可用于对小鼠基因组进行特定的改造。