Fan C Y, Potter P M, Rafferty J, Watson A J, Cawkwell L, Searle P F, O'Connor P J, Margison G P
Department of Chemical Carcinogenesis, Paterson Institute for Cancer Research, Manchester, UK.
Nucleic Acids Res. 1990 Oct 11;18(19):5723-7. doi: 10.1093/nar/18.19.5723.
A truncated human O6-alkylguanine-DNA-alkyltransferase (ATase) cDNA was ligated into an expression vector under the control of the mouse metallothionein-1 gene promotor and upstream of part of the human growth hormone gene to provide splice and polyadenylation signals. Transfection of this construct into human cells resulted in very high levels of ATase expression (more than 300 fmoles/mg protein versus less than 2 fm/mg protein in parent vector transfected control cells). Microinjection of a 4.2 kb fragment of this vector into B6D2F2 mouse embryos and implantation of survivors into pseudopregnant females has so far generated 35 offspring. Southern analysis of tail tip DNA has shown that 11 of the offspring are transgenic for the human ATase gene, between 1 and at least 30 copies of the gene being detected. Human ATase transcripts were detected in total RNA extracted from liver obtained from two male transgenic mice by partial hepatectomy. Cell free extracts of liver samples from five transgenic mice showed up to 4 times higher ATase levels than control livers.
将截短的人O6-烷基鸟嘌呤-DNA烷基转移酶(ATase)cDNA连接到受小鼠金属硫蛋白-1基因启动子控制且位于人生长激素基因部分序列上游的表达载体中,以提供剪接和聚腺苷酸化信号。将该构建体转染到人细胞中导致ATase的高水平表达(转染该构建体的细胞中为300多飞摩尔/毫克蛋白,而转染亲本载体的对照细胞中小于2飞摩尔/毫克蛋白)。将该载体的一个4.2 kb片段显微注射到B6D2F2小鼠胚胎中,并将存活的胚胎植入假孕雌性小鼠体内,到目前为止已产生35只后代。对尾尖DNA进行的Southern分析表明,11只后代为人ATase基因的转基因小鼠,检测到该基因的拷贝数在1至至少30个之间。通过部分肝切除术从两只雄性转基因小鼠的肝脏中提取的总RNA中检测到了人ATase转录本。来自五只转基因小鼠肝脏样本的无细胞提取物显示,其ATase水平比对照肝脏高4倍。