van Leeuwen Hans C, Liefhebber Jolanda M P, Spaan Willy J M
Department of Medical Microbiology, Center of Infectious Diseases, Leiden University Medical Center, Albinusdreef 2, 2300 RC Leiden, The Netherlands.
J Virol. 2006 May;80(9):4336-43. doi: 10.1128/JVI.80.9.4336-4343.2006.
The 3' nontranslated region (NTR) of the hepatitis C virus (HCV) genome is highly conserved and contains specific cis-acting RNA motifs that are essential in directing the viral replication machinery to initiate at the correct 3' end of the viral genome. Since the ends of viral genomes may be damaged by cellular RNases, preventing the initiation of viral RNA replication, stable RNA hairpin structures in the 3' NTR may also be essential in host defense against exoribonucleases. During 3'-terminal sequence analysis of serum samples of a patient with chronic hepatitis related to an HCV1b infection, a number of clones were obtained that were several nucleotides shorter at the extreme 3' end of the genome. These shorter 3' ends were engineered in selectable HCV replicons in order to enable the study of RNA replication in cell culture. When in vitro-transcribed subgenomic RNAs, containing shorter 3' ends, were introduced into Huh-7 cells, a few selectable colonies were obtained, and the 3' terminus of these subgenomic RNAs was sequenced. Interestingly, most genomes recovered from these colonies had regained the wild-type 3' ends, showing that HCV, like several other positive-stranded RNA viruses, has developed a strategy to repair deleted 3' end nucleotides. Furthermore, we found several genomes in these replicon colonies that contained a poly(A) tail and a short linker sequence preceding the poly(A) tail. After recloning and subsequent passage in Huh-7 cells, these poly(A) tails persisted and varied in length. In addition, the connecting linker became highly diverse in sequence and length, suggesting that these tails are actively replicated. The possible terminal repair mechanisms, including roles for the poly(A) tail addition, are discussed.
丙型肝炎病毒(HCV)基因组的3'非翻译区(NTR)高度保守,包含特定的顺式作用RNA基序,这些基序对于引导病毒复制机制在病毒基因组正确的3'末端起始至关重要。由于病毒基因组的末端可能会被细胞核糖核酸酶破坏,从而阻止病毒RNA复制的起始,因此3' NTR中的稳定RNA发夹结构对于宿主抵抗外切核糖核酸酶也可能至关重要。在对一名与HCV1b感染相关的慢性肝炎患者的血清样本进行3'末端序列分析时,获得了许多在基因组极端3'末端短几个核苷酸的克隆。这些较短的3'末端被构建到可选择的HCV复制子中,以便能够在细胞培养中研究RNA复制。当将含有较短3'末端的体外转录亚基因组RNA引入Huh-7细胞时,获得了一些可选择的菌落,并对这些亚基因组RNA的3'末端进行了测序。有趣的是,从这些菌落中回收的大多数基因组都恢复了野生型3'末端,表明HCV与其他几种正链RNA病毒一样,已经开发出一种修复缺失的3'末端核苷酸的策略。此外,我们在这些复制子菌落中发现了几个基因组,它们含有一个聚腺苷酸(poly(A))尾巴和在poly(A)尾巴之前的一个短连接序列。在重新克隆并随后在Huh-7细胞中传代后,这些poly(A)尾巴持续存在且长度各异。此外,连接接头在序列和长度上变得高度多样化,表明这些尾巴是被积极复制的。本文讨论了可能的末端修复机制,包括poly(A)尾巴添加的作用。