Guidotti L G, Matzke B, Pasquinelli C, Shoenberger J M, Rogler C E, Chisari F V
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037, USA.
J Virol. 1996 Oct;70(10):7056-61. doi: 10.1128/JVI.70.10.7056-7061.1996.
In this study, we examined the ability of the hepatitis B virus (HBV) precore, envelope, and X gene products to modulate HBV replication in the livers of transgenic mice that replicate the virus. Hepatic HBV replication was not affected by overexpression of the envelope or X gene products when these animals were crossed with transgenic mice that express the corresponding viral genes in the hepatocyte. Overexpression of the precore protein, however, eliminated nucleocapsid particles from the cytoplasm of the hepatocytes and abolished HBV replication without affecting the hepatic steady-state content of pregenomic HBV RNA. These observations suggest that the precore protein can exert a dominant negative effect on HBV replication, presumably at the level of nucleocapsid particle maturation or stability, suggesting an important role for this enigmatic viral protein in the HBV life cycle.
在本研究中,我们检测了乙肝病毒(HBV)前核心、包膜和X基因产物调节在肝脏中复制该病毒的转基因小鼠肝脏内HBV复制的能力。当这些动物与在肝细胞中表达相应病毒基因的转基因小鼠杂交时,肝脏HBV复制不受包膜或X基因产物过表达的影响。然而,前核心蛋白的过表达消除了肝细胞胞质中的核衣壳颗粒,并消除了HBV复制,而不影响前基因组HBV RNA的肝脏稳态含量。这些观察结果表明,前核心蛋白可能在核衣壳颗粒成熟或稳定性水平上对HBV复制发挥显性负效应,提示这种神秘的病毒蛋白在HBV生命周期中具有重要作用。