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真核 tRNA(Guanine--)甲基转移酶(Trm11-Trm112 复合物)甲基化所需的 tRNA 元素。

Required Elements in tRNA for Methylation by the Eukaryotic tRNA (Guanine--) Methyltransferase (Trm11-Trm112 Complex).

机构信息

Department of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama 790-8577, Japan.

出版信息

Int J Mol Sci. 2022 Apr 6;23(7):4046. doi: 10.3390/ijms23074046.

Abstract

The Trm11 and Trm112 complex (Trm11-Trm112) methylates the 2-amino group of guanosine at position 10 in tRNA and forms -methylguanosine. To determine the elements required in tRNA for methylation by Trm11-Trm112, we prepared 60 tRNA transcript variants and tested them for methylation by Trm11-Trm112. The results show that the precursor tRNA is not a substrate for Trm11-Trm112. Furthermore, the CCA terminus is essential for methylation by Trm11-Trm112, and Trm11-Trm112 also only methylates tRNAs with a regular-size variable region. In addition, the G10-C25 base pair is required for methylation by Trm11-Trm112. The data also demonstrated that Trm11-Trm112 recognizes the anticodon-loop and that U38 in tRNA acts negatively in terms of methylation. Likewise, the U32-A38 base pair in tRNA negatively affects methylation. The only exception in our in vitro study was tRNA. Our experiments showed that the tRNA transcript was slowly methylated by Trm11-Trm112. However, position 10 in this tRNA was reported to be unmodified G. We purified tRNA from wild-type and gene deletion strains and confirmed that a portion of tRNA is methylated by Trm11-Trm112 in . Thus, our study explains the mG10 modification pattern of all class I tRNAs and elucidates the Trm11-Trm112 binding sites.

摘要

Trm11 和 Trm112 复合物(Trm11-Trm112)将 tRNA 中第 10 位的鸟苷 2-氨基甲基化,形成 -甲基鸟苷。为了确定 Trm11-Trm112 甲基化 tRNA 所需的元件,我们制备了 60 种 tRNA 转录变体,并测试了它们是否被 Trm11-Trm112 甲基化。结果表明,前体 tRNA 不是 Trm11-Trm112 的底物。此外,CCA 末端对于 Trm11-Trm112 的甲基化是必需的,并且 Trm11-Trm112 仅甲基化具有正常大小可变区域的 tRNA。此外,G10-C25 碱基对对于 Trm11-Trm112 的甲基化是必需的。数据还表明 Trm11-Trm112 识别反密码子环,并且 tRNA 中的 U38 在甲基化方面起负作用。同样,tRNA 中的 U32-A38 碱基对对甲基化有负面影响。我们的体外研究中唯一的例外是 tRNA。我们的实验表明,tRNA 转录物被 Trm11-Trm112 缓慢甲基化。然而,据报道,该 tRNA 中的第 10 位是未修饰的 G。我们从野生型和基因缺失菌株中纯化了 tRNA,并证实了一部分 tRNA 被 Trm11-Trm112 在中甲基化。因此,我们的研究解释了所有 I 类 tRNA 的 mG10 修饰模式,并阐明了 Trm11-Trm112 的结合位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80d6/8999500/53295dfeaf47/ijms-23-04046-g001.jpg

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