Zhang Xin-Mei, Ng Alam Hoi-Lam, Tanner Julian A, Wu Wu-Tian, Copeland Neal G, Jenkins Nancy A, Huang Jian-Dong
Department of Biochemistry, University of Hong Kong, Faculty of Medicine Building, Pokfulam, Hong Kong SAR, China.
Genesis. 2004 Sep;40(1):45-51. doi: 10.1002/gene.20062.
The Purkinje neuron, one of the most fascinating components of the cerebellar cortex, is involved in motor learning, motor coordination, and cognitive function. Purkinje cell protein 2 (Pcp2/L7) expression is highly restricted to Purkinje and retinal bipolar cells, where it has been exploited to enable highly specific, Cre recombinase-mediated, site-specific recombination. Previous studies showed that mice carrying a Cre transgene produced by insertion of Cre cDNA into a small 2.88-kb Pcp2 DNA fragment expressed Cre in Purkinje cells; however, some Cre activity was also observed outside the target tissues. Here, we used Red-mediated recombineering to insert Cre cDNA into a 173-kb BAC carrying the entire intact Pcp2 gene, and characterize the resultant BAC/Cre transgenic mice for Cre expression. We show that BAC/Cre transgenic mice have exclusive Cre expression in Purkinje and bipolar cells and nowhere else. These mice will facilitate Purkinje cell and retinal bipolar cell-specific genetic manipulation.
浦肯野神经元是小脑皮质最引人入胜的组成部分之一,参与运动学习、运动协调和认知功能。浦肯野细胞蛋白2(Pcp2/L7)的表达高度局限于浦肯野细胞和视网膜双极细胞,利用这一特性可实现高度特异性的、由Cre重组酶介导的位点特异性重组。先前的研究表明,通过将Cre cDNA插入一个2.88 kb的小Pcp2 DNA片段而产生的携带Cre转基因的小鼠,在浦肯野细胞中表达Cre;然而,在靶组织之外也观察到了一些Cre活性。在这里,我们利用Red介导的重组工程将Cre cDNA插入一个携带完整Pcp2基因的173 kb细菌人工染色体(BAC)中,并对所得的BAC/Cre转基因小鼠的Cre表达进行了表征。我们发现,BAC/Cre转基因小鼠仅在浦肯野细胞和双极细胞中表达Cre,其他地方均无表达。这些小鼠将有助于进行浦肯野细胞和视网膜双极细胞特异性的基因操作。