Tronche François, Casanova Emilio, Turiault Marc, Sahly Iman, Kellendonk Christoph
CNRS FRE2401, Molecular Genetics, Neurophysiology and Behavior, Institute of Biology, Collège de France, 11 place Marcelin Berthelot, 75231 Cedex 5, Paris, France.
FEBS Lett. 2002 Oct 2;529(1):116-21. doi: 10.1016/s0014-5793(02)03266-0.
The use of site-specific recombinases enables the precise introduction of defined genetic mutations into the mouse genome. In theory, any deletion, point mutation, inversion or translocation can be modeled in mice. Because gene targeting is controlled both spatially and temporally, the function of a given gene can be studied in the desired cell types and at a specific time point. This 'genetic dissection' allows to define gene function in development, physiology or behavior. In this review, we focus on the technical possibilities of Cre and other site-specific recombinases but also discuss their limitations.
位点特异性重组酶的使用能够将特定的基因突变精确引入小鼠基因组。理论上,任何缺失、点突变、倒位或易位都可以在小鼠中建模。由于基因靶向在空间和时间上都受到控制,因此可以在所需的细胞类型和特定时间点研究给定基因的功能。这种“基因剖析”有助于确定基因在发育、生理或行为方面的功能。在本综述中,我们重点关注Cre和其他位点特异性重组酶的技术可能性,但也会讨论它们的局限性。