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The primer binding site on the RNA genome of human and simian immunodeficiency viruses is flanked by an upstream hairpin structure.

机译:人类和猿猴免疫缺陷病毒的RNA基因组上的引物结合位点两侧是上游发夹结构。

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摘要

Reverse transcription of retroviral genomes is primed by a tRNA molecule that anneals to an 18 nt primer binding site (PBS) on the viral RNA genome. Additional base pair interactions between the tRNA primer and the viral RNA have been proposed. In particular, base pairing was proposed between the anticodon loop of tRNALys3 and the 'A-rich' loop of a hairpin located immediately upstream of the PBS site in HIV-1 RNA. In order to judge the importance of this sequence/structure motif, we performed an extensive phylogenetic analysis of this genomic region in a variety of simian and human immunodeficiency viruses (SIV and HIV). Both the phylogeny of natural HIV/SIV sequences and the behaviour of U5-PBS mutant/revertant viruses support the idea that this RNA structure is critical for virus replication. Although this hairpin may play a role in tRNA annealing and/or initiation of reverse transcription, the proposed base pairing interaction between the A-rich loop of the HIV-1 hairpin and the anticodon of the initiator tRNA is not directly supported by this analysis.
机译:逆转录病毒基因组的逆转录由与病毒RNA基因组上的18 nt引物结合位点(PBS)退火的tRNA分子引发。已经提出了tRNA引物和病毒RNA之间的其他碱基对相互作用。特别地,提出了在tRNALys3的反密码子环与紧接在HIV-1 RNA PBS位点上游的发夹的“富A”环之间的碱基配对。为了判断此序列/结构基序的重要性,我们对各种猿猴和人类免疫缺陷病毒(SIV和HIV)中的该基因组区域进行了广泛的系统发育分析。天然HIV / SIV序列的系统发育和U5-PBS突变/回复病毒的行为都支持这种RNA结构对于病毒复制至关重要的想法。尽管此发夹可能在tRNA退火和/或反转录起始中发挥作用,但此分析未直接支持HIV-1发夹的富A环与引发剂tRNA的反密码子之间拟议的碱基配对相互作用。

著录项

  • 作者

    Berkhout, B;

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  • 年度 1997
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  • 原文格式 PDF
  • 正文语种 en
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