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Transfer RNA determinants for translational editing by Escherichia coli valyl-tRNA synthetase

机译:转移RNA决定簇以进行大肠杆菌valyl-tRNA合成酶的翻译编辑

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摘要

Valyl-tRNA synthetase (ValRS) has difficulty differentiating valine from structurally similar non-cognate amino acids, most prominently threonine. To minimize errors in aminoacylation and translation the enzyme catalyzes a proofreading (editing) reaction that is dependent on the presence of cognate tRNAVal. Editing occurs at a site functionally distinct from the aminoacylation site of ValRS and previous results have shown that the 3′-terminus of tRNAVal is recognized differently at the two sites. Here, we extend these studies by comparing the contribution of aminoacylation identity determinants to productive recognition of tRNAVal at the aminoacylation and editing sites, and by probing tRNAVal for editing determinants that are distinct from those required for aminoacylation. Mutational analysis of Escherichia coli tRNAVal and identity switch experiments with non-cognate tRNAs reveal a direct relationship between the ability of a tRNA to be aminoacylated and its ability to stimulate the editing activity of ValRS. This suggests that at least a majority of editing by the enzyme entails prior charging of tRNA and that misacylated tRNA is a transient intermediate in the editing reaction.
机译:缬氨酰-tRNA合成酶(ValRS)难以区分缬氨酸与结构相似的非同源氨基酸,最主要的是苏氨酸。为了最大程度地减少氨基酰化和翻译中的错误,该酶催化一个校对(编辑)反应,该反应取决于相关tRNA Val 的存在。编辑发生在功能上不同于ValRS的氨酰化位点的位点,先前的结果表明,tRNA Val 的3'末端在两个位点上的识别方式不同。在这里,我们通过比较氨基酰化同一性决定簇对tRNA Val 在氨基酰化和编辑位点的生产性识别的贡献,以及通过探测tRNA Val 来编辑决定簇来扩展这些研究。与氨基酰化所需的那些不同。大肠杆菌tRNA Val 的突变分析和非同源tRNA的身份转换实验表明,tRNA被氨基酰化的能力与其刺激ValRS编辑活性的能力之间存在直接关系。这表明该酶的至少大部分编辑需要在tRNA充电之前进行,并且酰化的tRNA是编辑反应中的瞬时中间体。

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