Will H, Cattaneo R, Pfaff E, Kuhn C, Roggendorf M, Schaller H
J Virol. 1984 May;50(2):335-42. doi: 10.1128/JVI.50.2.335-342.1984.
Recombinant DNA molecules consisting of the simian virus 40 (SV40) early region and different subgenomic hepatitis B virus DNA fragments were constructed in vitro and packaged in vivo into SV40 capsids by using a complementing SV40 helper virus. Upon infection with these virus stocks the three known hepatitis B-specific antigens were expressed under SV40 control. The surface antigen was released into the medium, and the core antigen and its derivative hepatitis B e antigen were only detected intracellularly. Size analysis of the core gene product(s) by immunoblotting revealed the presence of a single protein species identical with the 21-kilodalton core antigen isolated from human liver. The hepatitis B core antigen expressing construct did not contain a putative precore sequence, indicating that such a sequence is not needed for hepatitis B core antigen synthesis in animal cells. S1 analysis demonstrated the use of SV40 signals for initiation and polyadenylation of the core gene transcripts. In addition, a processing-polyadenylation signal was identified within the core gene.
由猿猴病毒40(SV40)早期区域和不同的亚基因组乙型肝炎病毒DNA片段组成的重组DNA分子在体外构建,并通过使用互补的SV40辅助病毒在体内包装到SV40衣壳中。用这些病毒储备感染后,三种已知的乙型肝炎特异性抗原在SV40控制下表达。表面抗原释放到培养基中,核心抗原及其衍生的乙型肝炎e抗原仅在细胞内检测到。通过免疫印迹对核心基因产物进行大小分析,结果显示存在一种与从人肝脏中分离出的21千道尔顿核心抗原相同的单一蛋白质。表达乙型肝炎核心抗原的构建体不包含推定的前核心序列,这表明动物细胞中乙型肝炎核心抗原的合成不需要这样的序列。S1分析表明,SV40信号用于核心基因转录本的起始和聚腺苷酸化。此外,在核心基因内鉴定出一个加工-聚腺苷酸化信号。