牛朊蛋白基因prnp敲除载体的构建及真核细胞转染

利用正负筛选策略(Positive-negative selection,PNS)对中靶细胞进行富集是提高体细胞基因打靶效率常用的策略之一。将动物的朊蛋白基因prnp敲除,使其不能表达朊蛋白(传染性海绵状脑病的致病蛋白),从而使其具有抵抗Prion病感染的能力。本研究采用正负筛选策略,构建了牛prnp基因的双等位基因敲除载体,经内切酶Sac Ⅱ线性化后,再通过电穿孔转染牛胎儿成纤维细胞,分别用600μg/mL G418、200nmol/mL Ganciclovir(GCV)进行正负药物筛选,最终获得了176个药物抗性细胞克隆,进一步采用PCR、测序、间接免疫荧光试验及Western blotting试验对细胞克隆进行鉴定,结果表明,其中的9个细胞克隆为中靶细胞,证明牛prnp基因被成功敲除。本研究为牛prnp的敲除提供了可行性依据,并为体细胞核移植生产敲除朊蛋白基因的转基因动物提供供体细胞。

Construction of prnp gene knockout vector and its transfection in eukaryotic cell

It is one of the frequently utilized strategies for positive-negative selection to elevate the gene targeting efficiency in somatic cells by enriching targeted colonies.Knocking outprnp in animals by gene targeting can prevent it from expressing Prion protein(Pathogenic protein of transmissible spongiform encephalopathy),which enables it to resist infection of Prion.We constructed a bovine prnp biallelic targeting vector via the positive-negative selection strategy,and ttamfected the lineadzed vector into the bovine fetal fibroblasts through electroporation.Then,we selected cells in cell culture medium with G418 under a concentration of 600 μg/mL followed bY Cranciclovir(GCV)under a concentration of 200 nmol/mL.In the end,we successfully obtained 176 cell clones.All these clones were identified by means of sequencing,immunofluorescence and western blotting,respectively,confirming that there existed 9 positive cell clones.The results showed that the bovine prnp gene was successfully knocked out.Conclusively,we provide an effective way to knockout bovine prnp gene.which could serve as the basis for producing prion protein gene knockout transgenic cloned cattle.