Günther S, Piwon N, Will H
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie an der Universität Hamburg, Federal Republic of Germany.
J Gen Virol. 1998 Feb;79 ( Pt 2):375-80. doi: 10.1099/0022-1317-79-2-375.
Hepatitis B virus (HBV) isolates with A-1762 to T and G-1764 to A mutations in the core promoter have been associated with active hepatitis, severe liver disease following liver transplantation, hepatocellular carcinoma and acute fulminant courses--in the latter case combined with a C-1653 to T mutation. In this study, a mutant core promoter region containing the T-1653, T-1762 and A-1764 mutations was placed into the context of a wild-type HBV genome and analysed by transfection. The mutations reduced the level of pre-C mRNA (by 55%) and e-antigen secretion. In contrast, no significant effects on the levels of pregenome/C and pre-S/S mRNAs, intracellular core, polymerase, and pre-S /S2 proteins and secreted S-antigen were observed. The amount of progeny virus DNA in the cells and in the culture medium was increased marginally, if at all.
核心启动子区发生A1762T和G1764A突变的乙型肝炎病毒(HBV)分离株与活动性肝炎、肝移植后严重肝病、肝细胞癌及急性暴发性病程相关,在后一种情况下还伴有C1653T突变。在本研究中,将含有T1653、T1762和A1764突变的突变核心启动子区置于野生型HBV基因组背景下,并通过转染进行分析。这些突变降低了前C mRNA水平(降低55%)和e抗原分泌。相比之下,未观察到对前基因组/C和前S/S mRNA水平、细胞内核蛋白、聚合酶、前S/S2蛋白及分泌的S抗原水平有显著影响。细胞内和培养基中子代病毒DNA的量即使有增加也很轻微。