Pugh J C, Weber C, Houston H, Murray K
J Med Virol. 1986 Nov;20(3):229-46. doi: 10.1002/jmv.1890200305.
The hepatitis B virus (HBV) genome carries an open reading frame of 462 bases, the X region, but the corresponding protein has yet to be identified as a natural product. In rodent cells cotransformed with the thymidine kinase gene of herpes simplex virus and HBV DNA, however, Gough [1983] identified a mRNA that hybridises uniquely with the X region of the HBV genome. A large fragment of the X region was inserted into plasmid pCL19 delta Y-T in order to produce, in Escherichia coli, the X gene product, HBxAg, as a polypeptide fused to the N-terminal part of the phage lambda cro gene product. Antisera raised against this fused polypeptide gave positive immunofluorescence reactions with the transformed rodent cells. This provides direct evidence for the expression of the HBxAg gene in eukaryotic cells transformed with HBV DNA. The approach used here should be generally applicable.
乙型肝炎病毒(HBV)基因组带有一个由462个碱基组成的开放阅读框,即X区,但相应的蛋白质尚未被鉴定为天然产物。然而,在与单纯疱疹病毒的胸苷激酶基因和HBV DNA共转化的啮齿动物细胞中,戈夫[1983]鉴定出一种mRNA,它能与HBV基因组的X区特异性杂交。将X区的一个大片段插入质粒pCL19 delta Y-T中,以便在大肠杆菌中产生X基因产物HBxAg,作为与噬菌体λ cro基因产物N端部分融合的多肽。针对这种融合多肽产生的抗血清与转化的啮齿动物细胞产生了阳性免疫荧光反应。这为HBxAg基因在经HBV DNA转化的真核细胞中的表达提供了直接证据。这里使用的方法应该具有普遍适用性。