DePrimo S E, Stambrook P J, Stringer J R
Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, OH 45267, USA.
Transgenic Res. 1996 Nov;5(6):459-66. doi: 10.1007/BF01980211.
The human placental alkaline phosphatase (PLAP) gene was analysed for its utility as a histochemically detectable reporter gene in transgenic mice. A reporter gene was made by linking the PLAP structural gene to an enhancer-promoter element from the human beta-actin gene. This gene was inserted into the mouse genome by transfection of embryonic stem cells, and by microinjection of fertilized eggs. Histochemical staining showed that the transgene was uniformly expressed in four of four stable ES cell lines, and in all ten tissues examined from adult animals from five lines of transgenic mice. Non-transgenic cells did not stain. These results suggest that the human PLAP gene will be of utility in studies requiring phenotypic marking of cells in tissues of mice.
对人胎盘碱性磷酸酶(PLAP)基因作为转基因小鼠中可通过组织化学检测的报告基因的效用进行了分析。通过将PLAP结构基因与人β-肌动蛋白基因的增强子-启动子元件连接,构建了一个报告基因。通过转染胚胎干细胞和显微注射受精卵,将该基因插入小鼠基因组。组织化学染色显示,转基因在四个稳定的胚胎干细胞系中的四个中均匀表达,并且在来自五个转基因小鼠品系的成年动物的所有十个检测组织中均有表达。非转基因细胞未染色。这些结果表明,人PLAP基因在需要对小鼠组织中的细胞进行表型标记的研究中将具有实用性。