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Selection of functional tRNA primers and primer binding site sequences from a retroviral combinatorial library: identification of new functional tRNA primers in murine leukemia virus replication

机译:从逆转录病毒组合文库中选择功能性tRNA引物和引物结合位点序列:鉴定鼠白血病病毒复制中的新功能性tRNA引物

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Retroviral reverse transcription is initiated from a cellular tRNA molecule and all known exogenous isolates of murine leukemia virus utilise a tRNAPro molecule. While several studies suggest flexibility in murine leukemia virus primer utilisation, studies on human immunodeficiency virus and avian retro-viruses have revealed evidence of molecular adapt-ation towards the specific tRNA isoacceptor used as replication primer. In this study, murine leukemia virus tRNA utilisation is investigated by in vivo screening of a retroviral vector combinatorial library with randomised primer binding sites. While most of the selected primer binding sites are complementary to the 3′-end of tRNAPro, we also retrieved PBS sequences matching four other tRNA molecules and demonstrate that Akv murine leukemia virus vectors may efficiently replicate using tRNAArg(CCU), tRNAPhe(GAA) and a hitherto unknown human tRNASer(CGA).
机译:逆转录病毒逆转录是从细胞tRNA分子开始的,所有已知的鼠白血病病毒外源分离株都利用tRNA Pro 分子。虽然有几项研究表明在鼠白血病病毒引物应用方面具有灵活性,但对人免疫缺陷病毒和禽逆转录病毒的研究表明,分子对适应用作复制引物的特定tRNA异构受体的适应性证据。在这项研究中,通过体内筛选具有随机引物结合位点的逆转录病毒载体组合文库,研究了鼠白血病病毒tRNA的利用。虽然大多数选定的引物结合位点与tRNA Pro 的3'末端互补,但我们还检索了与其他四个tRNA分子匹配的PBS序列,证明了Akv鼠白血病病毒载体可以使用tRNA Arg(CCU),tRNA Phe(GAA)和迄今未知的人tRNA Ser(CGA)有效复制。

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