Scaglioni P P, Melegari M, Wands J R
Molecular Hepatology Laboratory, Massachusetts General Hospital Cancer Center, Harvard Medical School, Charlestown 02129, USA.
Virology. 1997 Jul 7;233(2):374-81. doi: 10.1006/viro.1997.8594.
It is now well recognized that mutations in the hepatitis B virus (HBV) genome occur during the natural course of chronic viral infection. Regions of the viral genome that are frequently affected by such mutations, rearrangements, and/or deletions generally involve the precore promoter, precore, and core as well as the preS gene regions. However, little is known regarding the biologic consequences of these mutations on the functional properties of the variant viral strains with respect to effects on viral replication. In this study, we investigated the functional significance of precore promoter and precore gene mutations that reduce or abolish the synthesis of hepatitis B e antigen (HBeAg). We found that precore promoter mutations diminished the expression of HBeAg but did not affect the synthesis of pregenomic RNA. However, these precore mutations were associated with a modest increase in HBV replication. In contrast, a naturally occurring mutant that carries a termination codon in position 28 of the precore open reading frame demonstrated increased encapsidation of pregenomic mRNA into nucleocapsid particles. Consequently, this variant viral strain demonstrated a substantial increase in the level of viral replication compared to "wild-type" HBV and other precore promoter mutant viral strains. These studies suggest that substitutions in the precore promoter and precore gene not only alter the synthesis of HBeAg but also affect the level of viral replication.
现在人们已经充分认识到,在慢性病毒感染的自然过程中会发生乙型肝炎病毒(HBV)基因组的突变。病毒基因组中经常受到此类突变、重排和/或缺失影响的区域通常涉及前核心启动子、前核心和核心以及前S基因区域。然而,关于这些突变对变异病毒株功能特性在病毒复制影响方面的生物学后果,人们了解甚少。在本研究中,我们调查了降低或消除乙型肝炎e抗原(HBeAg)合成的前核心启动子和前核心基因突变的功能意义。我们发现前核心启动子突变减少了HBeAg的表达,但不影响前基因组RNA的合成。然而,这些前核心突变与HBV复制适度增加有关。相比之下,在前核心开放阅读框第28位携带终止密码子的天然突变体显示前基因组mRNA包装入核衣壳颗粒的增加。因此,与“野生型”HBV和其他前核心启动子突变病毒株相比,这种变异病毒株的病毒复制水平显著增加。这些研究表明,前核心启动子和前核心基因中的替代不仅改变了HBeAg的合成,还影响了病毒复制水平。