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The non-primate hepacivirus 5′ untranslated region possesses internal ribosomal entry site activity

机译:非灵长类肝炎病毒5非翻译区具有内部核糖体进入位点活性

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摘要

The 5′ untranslated region (5′UTR) of the recently described non-primate hepacivirus (NPHV) contains a region with sequence homology to the internal ribosomal entry site (IRES) of hepatitis C virus (HCV) and GB virus B (GBV-B). Here, we demonstrated internal translation initiation by the NPHV 5′UTR in a bicistronic vector. An RNA stem–loop upstream of the NPHV IRES was structurally distinct from corresponding regions in HCV and GBV-B, and was not required for IRES function. Insertion of the NPHV stem–loop into the corresponding region of the HCV 5′UTR within the HCV subgenomic replicon significantly impaired RNA replication, indicating that long-range interactions between the 5′UTR and cis-acting downstream elements within the NPHV genome are not interchangeable with those of HCV. Despite similarities in IRES structure and function between hepaciviruses, replication elements in the NPHV 5′UTR appear functionally distinct from those of HCV.
机译:最近描述的非灵长类肝炎病毒(NPHV)的5'非翻译区(5'UTR)包含与丙型肝炎病毒(HCV)和GB病毒B(GBV- B)。在这里,我们证明了双顺反子载体中NPHV 5'UTR的内部翻译起始。 NPHV IRES上游的RNA茎环在结构上与HCV和GBV-B中的相应区域不同,并且IRES功能不需要。将NPHV茎环插入HCV亚基因组复制子内HCV 5'UTR的相应区域中会严重损害RNA复制,表明5'UTR与NPHV基因组内顺式作用下游元件之间的远距离相互作用可与HCV互换。尽管肝炎病毒之间的IRES结构和功能相似,但是NPHV 5'UTR中的复制元件在功能上似乎与HCV不同。

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