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.
出处
《中国生物工程杂志》
CAS
CSCD
北大核心
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)
关键词
HBV转基因动物
培育
复制
稳定性
HBV transgenic animal Breeding Replication Stability