Ao A, Monk M, Lovell-Badge R, Melton D W
MRC Mammalian Development Unit, London, UK.
Development. 1988 Nov;104(3):465-71. doi: 10.1242/dev.104.3.465.
We have used a highly sensitive biochemical microassay to monitor the expression of a cloned minigene for hypoxanthine phosphoribosyl transferase (HPRT, EC.2.4.2.8) in preimplantation mouse embryos. The mouse HPRT promoter and the mouse metallothionein promoter (MT-I) function equally well in embryos at the 2-cell stage whereas the viral SV40 promoter does not allow HPRT expression. Induced HPRT activity from the MT-I HPRT minigene construct occurs in cleavage embryos cultured in the presence of cadmium. In contrast, negation of enzyme expression from the injected minigene DNA is mediated by simultaneous injection of HPRT antisense DNA.
我们使用了一种高度灵敏的生化微量分析法,来监测次黄嘌呤磷酸核糖基转移酶(HPRT,EC.2.4.2.8)的克隆小基因在植入前小鼠胚胎中的表达。小鼠HPRT启动子和小鼠金属硫蛋白启动子(MT-I)在2-细胞期胚胎中的功能同样良好,而病毒SV40启动子则不允许HPRT表达。来自MT-I HPRT小基因构建体的诱导HPRT活性出现在镉存在下培养的卵裂胚胎中。相反,通过同时注射HPRT反义DNA介导了注射的小基因DNA的酶表达的否定。