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作 者:孔祥平[1] 吴庆洲[1] 罗显荣[1] 胡莲美[1] 李秀梅[1] 易学瑞[1] 佟明华[1] 周军辉[1] 刘光泽[1]
机构地区:[1]解放军第458医院全军肝病中心转基因工程室,广州510602
出 处:《中国生物工程杂志》2008年第5期17-21,共5页China Biotechnology
基 金:广州市科技攻关计划-科技攻关引导项目(2005Z1-E4013)
摘 要:目的:提高复制型HBV转基因小鼠的遗传稳定性。方法:应用回交传代及双杂交育种法,经荧光定量PCR、ELISA和化学发光法研究HBV基因在小鼠体内的复制与表达。结果:HBV转基因小鼠已稳定传至第23代,血清HBsAg达4122.31±2044.74IU/ml,93.93%的转基因小鼠血清HBVDNA达10^4-10^4copies/ml,表达复制水平较早期有显著提高并稳定传代;雌雄小鼠之间表达水平无显著性差异。结论:该转基因小鼠经过培育传代,已成为一个高表达且遗传稳定的复制型HBV小鼠模型。Objective:To improve the genetic stability of HBV gene in transgenic mice. Methods: HBV transgenic mice were bred by backcross and double cross. The HBV gene expression and replication were studied with real-time PCR,ELISA and chemiluminescence. Results:The HBV transgenic mice have stably bred to 23^rd generation. The serum HBsAg level is 4122.31 ±2044.74IU/ml; The rate of HBV transgenic mice whose serum HBV DNA reach 10^4 - 10^6copies/ml was 93. 93%. The HBV replication and expression were improved markedly. There is no difference between male and female mice about serum HBsAg level. Conclusion:After breeding the HBV gene was expressed stably with high-level in transgenic mice.
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