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Importance of the reverse Hoogsteen base pair 54-58 for tRNA function

机译:反向Hoogsteen碱基对54-58对tRNA功能的重要性

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摘要

To elucidate the general constraints imposed on the structure of the D- and T-loops in functional tRNAs, active suppressor tRNAs were selected in vivo from a combinatorial tRNA gene library in which several nucleotide positions of these loops were randomized. Analysis of the nucleotide sequences of the selected clones demonstrates that among the randomized nucleotides, the most conservative are nucleotides 54 and 58 in the T-loop. In most cases, they make the combination U54-A58, which allows the formation of the normal reverse Hoogsteen base pair. Surprisingly, other clones have either the combination G54-A58 or G54-G58. However, molecular modeling shows that these purine–purine base pairs can very closely mimic the reverse Hoogsteen base pair U-A and thus can replace it in the T-loop of a functional tRNA. This places the reverse Hoogsteen base pair 54-58 as one of the most important structural aspects of tRNA functionality. We suggest that the major role of this base pair is to preserve the conformation of dinucleotide 59–60 and, through this, to maintain the general architecture of the tRNA L-form.
机译:为了阐明对功能性tRNA中D环和T环的结构施加的一般约束,从组合性tRNA基因库中选择了体内活性抑制性tRNA,其中这些环的几个核苷酸位置是随机的。对所选克隆的核苷酸序列的分析表明,在随机核苷酸中,最保守的是T环中的核苷酸54和58。在大多数情况下,它们会结合使用U54-A58,从而可以形成正常的反向Hoogsteen碱基对。令人惊讶地,其他克隆具有G54-A58或G54-G58的组合。但是,分子模型表明,这些嘌呤-嘌呤碱基对可以非常紧密地模仿反向Hoogsteen碱基对U-A,因此可以在功能性tRNA的T环中替代它。这使反向Hoogsteen碱基对54-58成为tRNA功能最重要的结构方面之一。我们建议,该碱基对的主要作用是保留二核苷酸59-60的构象,并以此维持tRNA L型的一般结构。

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