Evidence map›Paper›PMID 40650981›Full record

ArticleNucleic acids research2025

A transfer RNA methyltransferase with an unusual domain composition catalyzes 2'-O-methylation at position 6 in tRNA.

Teppei Matsuda, Ryota Yamagami, Aoi Ihara, Takeo Suzuki, Akira Hirata, Hiroyuki Hori

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Optimized tRNA structure-seq reveals robust tRNA secondary structures inbioRxiv : the preprint server for biology · 2026
    Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Teppei MatsudaDepartment of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan.
Ryota YamagamiDepartment of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan.ORCID 0000-0002-6947-1906
Aoi IharaDepartment of Nature Science, Faculty of Science and Technology, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima 770-8506, Japan.
Takeo SuzukiDepartment of Medical Biochemistry, Graduate School of Medicine, University of the Ryukyus, 1076 Kiyuna, Ginowan, Okinawa 901-2720, Japan.
Akira HirataDepartment of Nature Science, Faculty of Science and Technology, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima 770-8506, Japan.
Hiroyuki HoriDepartment of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan.

Funding

Institute for Fermentation, Osaka G-2024-2-059JAPAN Society for the Promotion of Science JP20H03211JAPAN Society for the Promotion of Science JP24K09352JAPAN Society for the Promotion of Science JP24K09381
6 · The paper itself

Abstract

Thermococcus kodakarensis tRNATrp contains 2'-O-methylcytidine at position 6 (Cm6). However, the tRNA methyltransferase responsible for the modification has not been identified. Using comparative genomics, we predicted TK1257 as a candidate gene for the modification enzyme. Biochemical and mass spectrometry studies of purified recombinant TK1257 gene product demonstrated that it possesses a tRNA methyltransferase activity for Cm6 formation. This protein has a highly unusual composition of domains, containing N-terminal ferredoxin-like, SPOUT catalytic, and THUMP domains. Previous to this study, all known THUMP-related tRNA methyltransferases were shown to contain a Rossmann fold catalytic domain and the nucleosides they produced were N2-methylguanosine and/or N2, N2-dimethylguanosine. Therefore, our findings extend the knowledge of architecture of tRNA methyltransferases. We named the TK1257 gene product TrmTS and showed that it can synthesize Am6 and Um6 as well as Cm6. A trmTS gene deletion strain showed slight growth retardation at high temperatures. Site-directed mutagenesis studies revealed catalytically and structurally important amino acid residues in TrmTS and identified a TrmTS-specific linker that is structurally essential. We revealed that TrmTS recognizes the 3'-CCA terminus of tRNA but does not require the three-dimensional structure of tRNA for its activity. Finally, we constructed a model of the binding between TrmTS and tRNA.

Indexed as

Archaeal ProteinsRNA, TransferThermococcustRNA MethyltransferasesAmino Acid SequenceCatalytic DomainCytidineMethylationModels, MolecularMutagenesis, Site-DirectedProtein DomainsArchaeal ProteinsCytidineRNA, TransfertRNA Methyltransferases

Identifiers

PMID40650981
PMCPMC12255305

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.