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The Simian Immunodeficiency Virus 5′ Untranslated Leader Sequence Plays a Role in Intracellular Viral Protein Accumulation and in RNA Packaging

机译:猿猴免疫缺陷病毒5未翻译的前导序列在细胞内病毒蛋白积累和RNA包装中起作用

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摘要

We investigated the role of 5′ untranslated leader sequences of simian immunodeficiency virus (SIVmac239) in RNA encapsidation and protein expression. A series of progressively longer deletion mutants was constructed with a common endpoint six nucleotides upstream of the gag initiation codon and another endpoint at the 3′ end of the primer binding site (PBS). We found that efficient intracellular Gag-Pol protein accumulation required the region between the PBS and splice donor (SD) site. Marked reduction of genomic RNA packaging was observed with all the deletion mutants that involved sequences at both the 5′ and at the 3′ ends of the major SD site, and increased nonspecific RNA incorporation could be detected in these mutants. RNA encapsidation was affected only modestly by a deletion of 54 nucleotides at the 3′ end of the SD site when the mutant construct pΔ54 was transfected alone. In contrast, the amount of pΔ54 genomic RNA incorporated into particles was reduced more than 10-fold when this mutant was cotransfected with a construct specifying an RNA molecule with a wild-type packaging signal. Therefore, we conclude that the 175 nucleotides located 5′ of the gag initiation codon are critical for efficient and selective incorporation of genomic RNA into virions. This location of the SIV Ψ element provides the means for efficient discrimination between viral genomic and spliced RNAs.
机译:我们调查了猿猴免疫缺陷病毒(SIVmac239)的5'非翻译前导序列在RNA衣壳化和蛋白质表达中的作用。构建了一系列逐渐更长的缺失突变体,其共同终点是gag起始密码子上游六个核苷酸,而另一个终点位于引物结合位点(PBS)的3'端。我们发现有效的细胞内Gag-Pol蛋白积累需要PBS和剪接供体(SD)站点之间的区域。用所有缺失突变体观察到基因组RNA包装的显着减少,这些缺失突变体在主要SD位点的5'和3'端均涉及序列,并且在这些突变体中可以检测到增加的非特异性RNA掺入。当突变体构建体pΔ54单独转染时,RNA衣壳仅受到SD位点3'端54个核苷酸缺失的轻微影响。相反,当将该突变体与指定具有野生型包装信号的RNA分子的构建体共转染时,掺入颗粒中的pΔ54基因组RNA的量减少了10倍以上。因此,我们得出结论,gag起始密码子5'处的175个核苷酸对于有效且选择性地将基因组RNA掺入病毒体至关重要。 SIVΨ元件的这一位置为有效区分病毒基因组和剪接的RNA提供了手段。

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