Rieveschl Laboratories for Mass Spectrometry, Department of Chemistry, University of Cincinnati, Cincinnati, Ohio, USA.
Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
J Bacteriol. 2019 Apr 9;201(9). doi: 10.1128/JB.00690-18. Print 2019 May 1.
tRNAs play a critical role in mRNA decoding, and posttranscriptional modifications within tRNAs drive decoding efficiency and accuracy. The types and positions of tRNA modifications in model bacteria have been extensively studied, and tRNA modifications in a few eukaryotic organisms have also been characterized and localized to particular tRNA sequences. However, far less is known regarding tRNA modifications in archaea. While the identities of modifications have been determined for multiple archaeal organisms, is the only organism for which modifications have been extensively localized to specific tRNA sequences. To improve our understanding of archaeal tRNA modification patterns and codon-decoding strategies, we have used liquid chromatography and tandem mass spectrometry to characterize and then map posttranscriptional modifications on 34 of the 35 unique tRNA sequences of A new posttranscriptionally modified nucleoside, 5-cyanomethyl-2-thiouridine (cnmsU), was discovered and localized to position 34. Moreover, data consistent with wyosine pathway modifications were obtained beyond the canonical tRNA as is typical for eukaryotes. The high-quality mapping of tRNA anticodon loops enriches our understanding of archaeal tRNA modification profiles and decoding strategies. While many posttranscriptional modifications in tRNAs are also found in bacteria and eukaryotes, several that are unique to archaea were identified. By RNA modification mapping, the modification profiles of tRNA anticodon loops were characterized, allowing a comparative analysis with modification profiles as well as a general comparison with bacterial and eukaryotic decoding strategies. This general comparison reveals that , like , follows codon-decoding strategies similar to those used by bacteria, although position 37 appears to be modified to a greater extent than seen in .
tRNAs 在 mRNA 解码中起着关键作用,tRNAs 中的转录后修饰可提高解码效率和准确性。模型细菌中的 tRNA 修饰类型和位置已经得到了广泛研究,少数真核生物中的 tRNA 修饰也已被确定并定位到特定的 tRNA 序列。然而,关于古菌中的 tRNA 修饰知之甚少。虽然已经确定了多种古菌的修饰类型,但 是唯一一种将修饰广泛定位到特定 tRNA 序列的生物体。为了更好地了解古菌 tRNA 修饰模式和密码子解码策略,我们使用液相色谱和串联质谱法对 35 个独特的 tRNA 序列中的 34 个进行了特征描述和位置分析。在位置 34 发现并定位了一个新的转录后修饰核苷,5-氰甲基-2-硫尿苷(cnmsU)。此外,还获得了超出典型真核生物的规范 tRNA 的类似于假尿嘧啶核苷途径修饰的数据。高质量的 tRNA 反密码子环映射丰富了我们对古菌 tRNA 修饰谱和解码策略的理解。虽然 tRNAs 中的许多转录后修饰也存在于细菌和真核生物中,但也发现了一些只存在于古菌中的修饰。通过 RNA 修饰映射,我们对 tRNA 反密码子环的修饰谱进行了特征描述,允许与 修饰谱进行比较分析,以及与细菌和真核解码策略进行一般比较。这种一般性比较表明, 与 一样,遵循类似于细菌的密码子解码策略,尽管位置 37 的修饰程度似乎比 中看到的更大。