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肝细胞Foxa2基因剔除小鼠的制备及鉴定
引用本文:张莉萍,Fulmer James.肝细胞Foxa2基因剔除小鼠的制备及鉴定[J].重庆医学,2005,34(6):890-891.
作者姓名:张莉萍  Fulmer James
作者单位:重庆医科大学附属第二医院临床检验中心,400010;美国宾夕法尼亚大学医学院遗传系
摘    要:目的制备肝细胞Foxa2基因特异性剔除的小鼠模型,并进行鉴定.方法采用CreloxP重组系统,在Cre重组酶的作用下,将小鼠肝细胞DNA上的Foxa2基因进行条件性的靶向剔除;并通过PCR和免疫荧光染色法进行鉴定.结果PCR在剔除型小鼠中未扩增出Foxa2基因的条带;同时定量分析也未测出其mRNA的表达;免疫荧光显示剔除型小鼠的Foxa2蛋白也为阴性.结论条件性基因剔除技术能成功地制备肝细胞Foxa2基因特异性剔除的小鼠模型.

关 键 词:Foxa2基因  肝细胞  基因剔出  聚合酶联反应
文章编号:1671-8348(2005)06-0890-02

Generation and confirmation of Foxa2 gene knockout in hepatocyte in mice
ZHANG Li-ping,Fulmer James.Generation and confirmation of Foxa2 gene knockout in hepatocyte in mice[J].Chongqing Medical Journal,2005,34(6):890-891.
Authors:ZHANG Li-ping  Fulmer James
Abstract:s:Objective To generate Foxa2 loxP/loxPAFP.Cre mice and confirm the genetype.Methods Cre-loxP system was introduced to mediate targeting of the Foxa2 gene and to achieve hepatocyte specific expression of Cre; real-time PCR and immunofluorescence staining were used to confirm absence of Foxa2 in livers from Foxa2 loxP/loxPAFP.Cre mice.Results There is no band for Foxa2 by PCR, no Foxa2 mRNA expression by real-time PCR in Foxa2 loxP/loxPAFP.Cre mice.Conclusion Foxa2 is deleted efficiently in Foxa2 loxP/loxPAFP.Cre mice by conditional gene knockout.
Keywords:Foxa2 gene  hepatocyte  gene knockout
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