Tsien J Z, Chen D F, Gerber D, Tom C, Mercer E H, Anderson D J, Mayford M, Kandel E R, Tonegawa S
Howard Hughes Medical Institute, Center for Learning and Memory, Massachusetts Institute of Technology, Cambridge 02139, USA.
Cell. 1996 Dec 27;87(7):1317-26. doi: 10.1016/s0092-8674(00)81826-7.
Using the phage P1-derived Cre/loxP recombination system, we have developed a method to create mice in which the deletion (knockout) of virtually any gene of interest is restricted to a subregion or a specific cell type in the brain such as the pyramidal cells of the hippocampal CA1 region. The Cre/loxP recombination-based gene deletion appears to require a certain level of Cre protein expression. The brain subregional restricted gene knockout should allow a more precise analysis of the impact of a gene mutation on animal behaviors.
利用源自噬菌体P1的Cre/loxP重组系统,我们开发了一种方法来创建小鼠,在这种小鼠中,几乎任何感兴趣基因的缺失(敲除)都局限于大脑的一个亚区域或特定细胞类型,如海马CA1区的锥体细胞。基于Cre/loxP重组的基因缺失似乎需要一定水平的Cre蛋白表达。大脑亚区域受限的基因敲除应该能够更精确地分析基因突变对动物行为的影响。