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Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites

机译:微小核糖核酸病毒聚合酶在由马铃薯病毒衍生的转录滑动位点上滑动的倾向

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摘要

The substitution rates of viral polymerases have been studied extensively. However less is known about the tendency of these enzymes to ‘slip’ during RNA synthesis to produce progeny RNAs with nucleotide insertions or deletions. We recently described the functional utilization of programmed polymerase slippage in the family Potyviridae. This slippage results in either an insertion or a substitution, depending on whether the RNA duplex realigns following the insertion. In this study we investigated whether this phenomenon is a conserved feature of superfamily I viral RdRps, by inserting a range of potyvirus-derived slip-prone sequences into a picornavirus, Theiler’s murine encephalomyelitis virus (TMEV). Deep-sequencing analysis of viral transcripts indicates that the TMEV polymerase ‘slips’ at the sequences U6–7 and A6–7 to insert additional nucleotides. Such sequences are under-represented within picornaviral genomes, suggesting that slip-prone sequences create a fitness cost. Nonetheless, the TMEV insertional and substitutional spectrum differed from that previously determined for the potyvirus polymerase.
机译:病毒聚合酶的取代率已被广泛研究。然而,人们对这些酶在RNA合成过程中“滑移”以产生带有核苷酸插入或缺失的后代RNA的趋势了解较少。我们最近描述了程序化聚合酶滑移在Potyviridae家族中的功能利用。这种滑移会导致插入或取代,具体取决于RNA双链体在插入后是否重新排列。在这项研究中,我们通过将一系列由马铃薯病毒衍生的易滑序列插入到微小RNA病毒(泰勒的鼠脑脊髓炎病毒(TMEV))中,研究了这一现象是否是超家族I病毒RdRps的保守特征。病毒转录本的深度测序分析表明,TMEV聚合酶在“ U6–7”和“ A6–7”序列上“滑动”以插入其他核苷酸。此类序列在微核病毒基因组中的代表性不足,表明易发生滑脱的序列会产生健身成本。尽管如此,TMEV的插入和取代谱不同于先前确定的针对杯状病毒聚合酶的谱。

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