Hepatitis B virus polymerase suppresses translation of pregenomic RNA via a mechanism involving its interaction with 5′ stem-loop structure

被引:28
|
作者
Ryu, Dong-Kyun [1 ]
Kim, Seahee [1 ]
Ryu, Wang-Shick [1 ]
机构
[1] Yonsei Univ, Dept Biochem, Seoul 120749, South Korea
关键词
hepatitis B virus; polymerase; stem-loop structure; translation; encapsidation;
D O I
10.1016/j.virol.2007.11.010
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The pregenomic RNA (pgRNA) of hepadnaviruses serves a dual role: as mRNA for the core (C) and polymerase (P) synthesis and as an RNA template for viral genome replication. A question arises as to how these two roles are regulated. We hypothesized that the P protein could suppress translation of the pgRNA via its interaction with 5' stem-loop structure (F or encapsidation signal). Consistent with the hypothesis, we observed up-regulation of the C protein level in the absence of the P protein expression in a physiological context. Importantly, translational suppression depended on the 5' epsilon sequence. Furthermore, the impact of the P protein on ongoing translation of the C ORF was directly demonstrated by polysome distribution analysis. We conclude that the P protein suppresses translation of the pgRNA via a mechanism involving its interaction with the 5' epsilon sequence, a finding that implicates the coordinated switch from translation to genome replication. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:112 / 123
页数:12
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