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3-(3-氨基-3-羧丙基)-5,6-二氢尿嘧啶核苷是来自布氏锥虫 tRNALys(UUU) 的两种新型转录后修饰之一。

3-(3-amino-3-carboxypropyl)-5,6-dihydrouridine is one of two novel post-transcriptional modifications in tRNALys(UUU) from Trypanosoma brucei.

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

出版信息

FEBS J. 2011 Dec;278(24):4782-96. doi: 10.1111/j.1742-4658.2011.08379.x. Epub 2011 Oct 28.

Abstract

tRNA is the most heavily modified of all RNA types, with typically 10-20% of the residues being post-transcriptionally altered. Unravelling the modification pattern of a tRNA is a challenging task; there are 92 currently known tRNA modifications, many of which are chemically similar. Furthermore, the tRNA has to be investigated with single-nucleotide resolution in order to ensure complete mapping of all modifications. In the present work, we characterized tRNA(Lys)(UUU) from Trypanosoma brucei, and provide a complete overview of its post-transcriptional modifications. The first step was MALDI-TOF MS of two independent digests of the tRNA, with RNase A and RNase T1, respectively. This revealed digestion products harbouring mass-changing modifications. Next, the modifications were mapped at the nucleotide level in the RNase products by tandem MS. Comparison with the sequence of the unmodified tRNA revealed the modified residues. The modifications were further characterized at the nucleoside level by chromatographic retention time and fragmentation pattern upon higher-order tandem MS. Phylogenetic comparison with modifications in tRNA(Lys) from other organisms was used through the entire analysis. We identified modifications on 12 nucleosides in tRNA(Lys)(UUU), where U47 exhibited a novel modification, 3-(3-amino-3-carboxypropyl)-5,6-dihydrouridine, based on identical chromatographic retention and MS fragmentation as the synthetic nucleoside. A37 was observed in two versions: a minor fraction with the previously described 2-methylthio-N(6)-threonylcarbamoyl-modification, and a major fraction with A37 being modified by a 294.0-Da moiety. The latter product is the largest adenosine modification reported so far, and we discuss its nature and origin.

摘要

tRNA 是所有 RNA 类型中修饰程度最高的,通常有 10-20%的残基在转录后发生改变。解析 tRNA 的修饰模式是一项具有挑战性的任务;目前已知有 92 种 tRNA 修饰,其中许多在化学上是相似的。此外,为了确保所有修饰都能被完整地绘制出来,tRNA 必须以单核苷酸分辨率进行研究。在本工作中,我们对来自锥虫的 tRNA(Lys)(UUU)进行了表征,并提供了其转录后修饰的完整概述。第一步是对 tRNA 进行两种独立的酶切消化,分别使用 RNase A 和 RNase T1,然后用 MALDI-TOF MS 进行分析。这揭示了含有质量变化修饰的酶切产物。接下来,通过串联 MS 在 RNase 产物中对修饰进行核苷酸水平的定位。与未修饰 tRNA 的序列进行比较,揭示了修饰的残基。通过更高阶串联 MS 的色谱保留时间和碎片模式对修饰核苷进行了进一步的特征描述。通过整个分析过程,将与其他生物体中的 tRNA(Lys)修饰进行了系统发育比较。我们在 tRNA(Lys)(UUU)中鉴定出 12 个核苷上的修饰,其中 U47 表现出一种新的修饰,即基于与合成核苷相同的色谱保留和 MS 碎片,3-(3-氨基-3-羧基丙基)-5,6-二氢尿嘧啶。A37 观察到两种版本:一种是以前描述的 2-甲硫基-N(6)-苏氨酰碳酰胺修饰的少量部分,另一种是 A37 被 294.0-Da 部分修饰的主要部分。后一种产物是迄今为止报道的最大的腺嘌呤修饰,我们讨论了它的性质和来源。

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