Yamagami Ryota, Takahashi Kojiro, Shingu Shogo, Namba Miyu, Kamizaki Kohsuke, Hori Hiroyuki
Department of Applied Chemistry, Graduate School of Science and Engineering, Ehime University, Matsuyama, Ehime 790-8577, Japan
Department of Applied Chemistry, Graduate School of Science and Engineering, Ehime University, Matsuyama, Ehime 790-8577, Japan.
RNA. 2025 May 16;31(6):850-867. doi: 10.1261/rna.080405.125.
Pseudouridine is a modified nucleoside found in various RNA species, including tRNA, rRNA, mRNA, and other noncoding RNAs. Pseudouridine is synthesized from uridine by pseudouridine synthases. While the landscape of pseudouridines in RNA has been extensively studied, much less is known about substrate RNA recognition mechanisms of pseudouridine synthases. Herein, we investigate the tRNA pseudouridine synthase D (TruD), which catalyzes the formation of pseudouridine at position 13 in tRNA in , a thermophilic eubacterium. To identify the tRNA substrates of TruD, we compared results of next-generation sequencing experiments combined with bisulfite probing of pseudouridine in tRNAs from both wild-type and a gene disruption mutant. Our data reveal that TruD recognizes tRNA, tRNA, and tRNA as substrate tRNAs. In addition, we discover that TruD modifies U35 in tRNA, which has previously been reported as a substrate of RluF in These findings were validated through in vitro assays with recombinant TruD, which further demonstrated that TruD can act on other RNAs, including a CDC8 mRNA fragment, a known substrate of Pus7, the eukaryotic counterpart of TruD. Systematic mutational analysis of CDC8 transcripts reveals that TruD preferentially pseudouridylates the UNAR sequence in tRNA substrates (N = any nucleotide, R = purine, = target site). Finally, we identify over 600 mRNA fragments containing this recognition sequence in ORFs and demonstrate the ability of TruD to act on these potential mRNA substrates. Our findings suggest the possibility that many other RNAs are modified by TruD in vivo.
假尿苷是一种在多种RNA种类中发现的修饰核苷,包括转运RNA(tRNA)、核糖体RNA(rRNA)、信使RNA(mRNA)和其他非编码RNA。假尿苷由尿苷通过假尿苷合酶合成。虽然RNA中假尿苷的情况已得到广泛研究,但关于假尿苷合酶的底物RNA识别机制却知之甚少。在此,我们研究了tRNA假尿苷合酶D(TruD),它催化嗜热真细菌中tRNA第13位假尿苷的形成。为了鉴定TruD的tRNA底物,我们比较了下一代测序实验结果,并结合了对野生型和基因破坏突变体的tRNA中假尿苷的亚硫酸氢盐探测。我们的数据表明,TruD将tRNA、tRNA和tRNA识别为底物tRNA。此外,我们发现TruD修饰tRNA中的U35,此前曾报道其为RluF的底物。这些发现通过用重组TruD进行的体外测定得到验证,进一步证明TruD可以作用于其他RNA,包括CDC8 mRNA片段,它是TruD的真核对应物Pus7的已知底物。对CDC8转录本的系统突变分析表明,TruD优先使tRNA底物中的UNAR序列假尿苷化(N = 任何核苷酸,R =嘌呤, = 靶位点)。最后,我们在ORF中鉴定出600多个含有该识别序列的mRNA片段,并证明TruD能够作用于这些潜在的mRNA底物。我们的发现表明,体内许多其他RNA可能被TruD修饰。