Lu D J, Zheng H L, Xi J Y, Zhang T, Chen X M, Lu F M
Department of Microbiology and Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
Department of Microbiology and Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China; Peking University People's Hospital, Peking University Hepatology Institute, Beijing 100044, China.
Zhonghua Gan Zang Bing Za Zhi. 2021 Oct 20;29(10):1035-1040. doi: 10.3760/cma.j.cn501113-20210808-00384.
Hepatitis B virus (HBV) is an important pathogen that causes different liver diseases such as viral hepatitis and liver cirrhosis. HBV pregenomic RNA (pgRNA) plays a crucial role in HBV life cycle, which is not only the translation template of core (C) and polymerase (P), but also the template of reverse transcription. The ratio of P protein to core protein is tightly regulated. Since P and core are both translated by pgRNA and the open reading frame (ORF) of P is located downstream of the ORF of core, how to initiate P protein translation is a key scientific question. Previous studies suggest that P can be translated through different mechanisms, such as leaky scanning and reinitiation. In this review, we summarized the proposed mechanisms relevant to the translation of polymerase from HBV pgRNA through literature review and derivation.
乙型肝炎病毒(HBV)是一种重要的病原体,可导致病毒性肝炎和肝硬化等不同的肝脏疾病。HBV前基因组RNA(pgRNA)在HBV生命周期中起着至关重要的作用,它不仅是核心蛋白(C)和聚合酶(P)的翻译模板,也是逆转录的模板。P蛋白与核心蛋白的比例受到严格调控。由于P蛋白和核心蛋白均由pgRNA翻译而来,且P蛋白的开放阅读框(ORF)位于核心蛋白ORF的下游,因此如何启动P蛋白的翻译是一个关键的科学问题。以往的研究表明,P蛋白可以通过不同的机制进行翻译,如渗漏扫描和重新起始。在本综述中,我们通过文献综述和推导,总结了与HBV pgRNA聚合酶翻译相关的机制。