Ceriotti Luis F, Warren Jessica M, Sanchez-Puerta M Virginia, Sloan Daniel B
IBAM, Universidad Nacional de Cuyo, CONICET, Facultad de Ciencias Agrarias, Mendoza, Argentina.
Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Mendoza, Argentina.
Plant J. 2024 Dec;120(6):2784-2802. doi: 10.1111/tpj.17146. Epub 2024 Nov 18.
The function of transfer RNAs (tRNAs) depends on enzymes that cleave primary transcript ends, add a 3' CCA tail, introduce post-transcriptional base modifications, and charge (aminoacylate) mature tRNAs with the correct amino acid. Maintaining an available pool of the resulting aminoacylated tRNAs is essential for protein synthesis. High-throughput sequencing techniques have recently been developed to provide a comprehensive view of aminoacylation state in a tRNA-specific fashion. However, these methods have never been applied to plants. Here, we treated Arabidopsis thaliana RNA samples with periodate and then performed tRNA-seq to distinguish between aminoacylated and uncharged tRNAs. This approach successfully captured every tRNA isodecoder family and detected expression of additional tRNA-like transcripts. We found that estimated aminoacylation rates and CCA tail integrity were significantly higher on average for organellar (mitochondrial and plastid) tRNAs than for nuclear/cytosolic tRNAs. Reanalysis of previously published human cell line data showed a similar pattern. Base modifications result in nucleotide misincorporations and truncations during reverse transcription, which we quantified and used to test for relationships with aminoacylation levels. We also determined that the Arabidopsis tRNA-like sequences (t-elements) that are cleaved from the ends of some mitochondrial messenger RNAs have post-transcriptionally modified bases and CCA-tail addition. However, these t-elements are not aminoacylated, indicating that they are only recognized by a subset of tRNA-interacting enzymes and do not play a role in translation. Overall, this work provides a characterization of the baseline landscape of plant tRNA aminoacylation rates and demonstrates an approach for investigating environmental and genetic perturbations to plant translation machinery.
转运RNA(tRNA)的功能依赖于多种酶,这些酶可切割初级转录本末端、添加3' CCA尾、引入转录后碱基修饰,并将正确的氨基酸装载(氨酰化)到成熟的tRNA上。维持由此产生的氨酰化tRNA的可用库对于蛋白质合成至关重要。最近开发的高通量测序技术能够以tRNA特异性方式全面呈现氨酰化状态。然而,这些方法从未应用于植物。在此,我们用高碘酸盐处理拟南芥RNA样本,然后进行tRNA测序以区分氨酰化和未装载的tRNA。这种方法成功捕获了每个tRNA同功异构体家族,并检测到了其他tRNA样转录本的表达。我们发现,细胞器(线粒体和质体)tRNA的平均估计氨酰化率和CCA尾完整性显著高于核/胞质tRNA。对先前发表的人类细胞系数据的重新分析显示了类似的模式。碱基修饰会导致逆转录过程中的核苷酸错掺入和截短,我们对其进行了量化,并用于测试与氨酰化水平的关系。我们还确定,从一些线粒体信使RNA末端切割下来的拟南芥tRNA样序列(t元件)具有转录后修饰的碱基和CCA尾添加。然而,这些t元件没有被氨酰化,这表明它们仅被一部分与tRNA相互作用的酶识别,并且在翻译中不起作用。总体而言,这项工作对植物tRNA氨酰化率的基线情况进行了表征,并展示了一种研究植物翻译机制的环境和遗传扰动的方法。