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Evidence for an RNA pseudoknot loop-helix interaction essential for efficient −1 ribosomal frameshifting

机译:RNA假结环螺旋相互作用对于有效的-1核糖体移码必不可少的证据

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摘要

RNA pseudoknots are structural elements that participate in a variety of biological processes. At −1 ribosomal frameshifting sites, several types of pseudoknot have been identified which differ in their organisation and functionality. The pseudoknot found in infectious bronchitis virus (IBV) is typical of those that possess a long stem 1 of 11-12 bp and a long loop 2 (30-164 nt). A second group of pseudoknots are distinguishable that contain stems of only 5 to 7 bp and shorter loops. The NMR structure of one such pseudoknot, that of mouse mammary tumor virus (MMTV), has revealed that it is kinked at the stem 1-stem 2 junction, and that this kinked conformation is essential for efficient frameshifting. We recently investigated the effect on frameshifting of modulating stem 1 length and stability in IBV-based pseudoknots, and found that a stem 1 with at least 11 bp was needed for efficient frameshifting. Here, we describe the sequence manipulations that are necessary to bypass the requirement for an 11 bp stem 1 and to convert a short non-functional IBV-derived pseudoknot into a highly efficient, kinked frameshifter pseudoknot. Simple insertion of an adenine residue at the stem 1-stem 2 junction (an essential feature of a kinked pseudoknot) was not sufficient to create a functional pseudoknot. An additional change was needed: efficient frameshifting was recovered only when the last nucleotide of loop 2 was changed from a G to an A. The requirement for an A at the end of loop 2 is consistent with a loop-helix contact similar to those described in other RNA tertiary structures. A mutational analysis of both partners of the proposed interaction, the loop 2 terminal adenine residue and two G·C pairs near the top of stem 1, revealed that the interaction was essential for efficient frameshifting. The specific requirement for a 3′-terminal A residue was lost when loop 2 was increased from 8 to 14 nt, suggesting that the loop-helix contact may be required only in those pseudoknots with a short loop 2.
机译:RNA假结是参与多种生物学过程的结构元件。在-1个核糖体移码位点,已鉴定出几种假结,它们的组织和功能不同。传染性支气管炎病毒(IBV)中发现的假结是典型的假茎,其茎长为11-12 bp,长环为2(30-164 nt)。第二组假结是可区分的,其仅包含5至7 bp的茎和较短的环。小鼠乳腺肿瘤病毒(MMTV)的一个这样的假结的NMR结构表明,它在茎1茎2连接处扭结,并且该扭结构象对于有效的移码是必不可少的。我们最近研究了在基于IBV的假结中调节茎1长度和稳定性对移码的影响,并发现有效移码需要至少11 bp的茎1。在这里,我们描述了绕开11 bp茎1的需求并将短的非功能性IBV衍生的假结转换为高效,扭结的移框假结所必需的序列操作。仅在茎1茎2连接处插入一个腺嘌呤残基(扭结假结的基本特征)不足以产生功能性假结。还需要进行其他更改:仅当环2的最后一个核苷酸从G变为A时,才能恢复有效的移码。在环2末尾对A的要求与类似于所述的环-螺旋接触是一致的在其他RNA三级结构中。对提议的相互作用的两个伙伴,第2环末端腺嘌呤残基和茎1顶部附近的两个G·C对进行突变分析,结果表明,相互作用对于有效的移码至关重要。当将环2从8 nt增加到14 nt时,失去了3'端A残基的特定要求,这表明仅在具有短环2的那些假结中可能需要环-螺旋接触。

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