Wang Y, Schäfer-Ridder M, Stratowa C, Wong T K, Hofschneider P H
EMBO J. 1982;1(10):1213-6. doi: 10.1002/j.1460-2075.1982.tb00015.x.
Hepatitis B virus (HBV) DNA was isolated from the recombinant plasmid pA01 -HBV and recircularized . Immediately after introduction of this DNA into mouse fibroblasts (NIH 3T3) we observed increasing release of hepatitis B surface antigen (HBsAg) into the culture medium. Later production of HBsAg declined to a lower but constant level. No dominant selective marker and foreign promoter were necessary in this system, which therefore can be used for the study of regulation of HBsAg expression.
从重组质粒pA01 - HBV中分离出乙肝病毒(HBV)DNA并使其环化。将该DNA导入小鼠成纤维细胞(NIH 3T3)后,我们立即观察到乙肝表面抗原(HBsAg)向培养基中的释放量增加。随后,HBsAg的产量下降至较低但稳定的水平。该系统无需显性选择标记和外源启动子,因此可用于研究HBsAg表达的调控。