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Unusual dicistronic expression from closely spaced initiation codons in an umbravirus subgenomic RNA

机译:从伞形病毒亚基基质RNA中的紧密间隔的引发密码子的异常角色表达

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Translation commencing at closely spaced initiation codons is common in RNA viruses with limited genome space. In the subgenomic RNA (sgRNA) of Pea enation mosaic virus 2, two closely spaced, out-of-frame start codons direct synthesis of movement/stability proteins p26 and p27. Efficient translation from AUG(26)/AUG(27) is dependent on three 3'-proximal cap-independent translation enhancers (3'CITEs), whereas translation of the genomic (gRNA) requires only two. Contrary to strictly scanning-dependent initiation at the gRNA, sequence context of AUG(26)/AUG(27) does not conform with Kozak requirements and insertion of efficient upstream AUGs had pronounced effects for AUG(26) but only moderate effects for AUG27. Insertion of a hairpin within an extended 5'UTR did not significantly impact translation from AUG(26)/AUG(27). Furthermore, AUG(27) repressed translation from upstream AUG(26) and this effect was mitigated when inter-codon spacing was reduced. Addition of a stable hairpin to the very 5' end of the sgRNA severely restricted translation, testifying that this 3'CITE-driven initiation is 5' end-dependent. Similar to gRNA, sgRNA reporter transcripts were nearly exclusively associated with light polysomes and 3'CITE-promoted long-distance interaction connecting the sgRNA ends affected the number of templates translated and not the initiation rate. We propose a non-canonical, 3' CITE-driven mechanism for efficient dicistronic expression from umbravirus sgRNAs.
机译:在紧密间隔的启动密码子中开始翻译在具有有限的基因组空间的RNA病毒中常见。在豌豆雌节病病毒2的亚基组科(SGRNA)中,两个紧密间隔的,框架外开始密码子直接合成运动/稳定性蛋白P26和P27。 8月(26)/ 8月(27)的有效翻译依赖于三个3'-近端帽独立的翻译增强剂(3'cites),而基因组(GRNA)的翻译只需要两种。与GRNA的严格扫描依赖性启动相反,AUG(26)/ 8月(27)的序列背景不符合Kozak要求,并插入AUGS的高效上游效果(26),但仅在8月27日效应。在延长的5'UTR中插入发夹并没有显着影响到8月(26)/ 8月(27)。此外,Aug(27)来自Upstream(26)的压抑翻译(26),并且当互编码间距减少时,减轻了这种效果。添加稳定的发夹到SGRNA的5'末端严重限制翻译,作证,这3'Cite驱动的启动是5'终端依赖性。与GRNA类似,SGRNA报告转录物几乎完全与光多肌元和3'Cite促进的长距离相互作用相关,连接SGRNA结束影响了转换的模板的数量而不是发起率。我们提出了一种非规范,3'引用的机制,用于乌伐韦斯斯乌斯诺斯的高效二次调整性表达。

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