Evidence map›Paper›PMID 31361898›Full record

ArticleNucleic acids research2019

FICC-Seq: a method for enzyme-specified profiling of methyl-5-uridine in cellular RNA.

Jean-Michel Carter, Warren Emmett, Igor Rdl Mozos, Annika Kotter, Mark Helm, Jernej Ule, Shobbir Hussain

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

45 citing papers in PubMed, 79 citations in OpenAlex.

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  13. Conserved 5-methyluridine tRNA modification modulates ribosome translocation.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

7 authors at 3 institutions in 2 countries.

Jean-Michel CarterDepartment of Biology and Biochemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Warren EmmettThe Francis-Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Igor Rdl MozosThe Francis-Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Annika KotterJohannes Gutenberg-Universität, Institut für Pharmazie und Biochemie, Staudinger Weg 5, 55128 Mainz, Germany.
Mark HelmJohannes Gutenberg-Universität, Institut für Pharmazie und Biochemie, Staudinger Weg 5, 55128 Mainz, Germany.
Jernej UleThe Francis-Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Shobbir HussainDepartment of Biology and Biochemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
The Francis Crick Institute · GBJohannes Gutenberg University Mainz · DEUniversity of Bath · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N000749/1
6 · The paper itself

Abstract

Methyl-5-uridine (m5U) is one the most abundant non-canonical bases present in cellular RNA, and in yeast is found at position U54 of tRNAs where modification is catalysed by the methyltransferase Trm2. Although the mammalian enzymes that catalyse m5U formation are yet to be identified via experimental evidence, based on sequence homology to Trm2, two candidates currently exist, TRMT2A and TRMT2B. Here we developed a genome-wide single-nucleotide resolution mapping method, Fluorouracil-Induced-Catalytic-Crosslinking-Sequencing (FICC-Seq), in order to identify the relevant enzymatic targets. We demonstrate that TRMT2A is responsible for the majority of m5U present in human RNA, and that it commonly targets U54 of cytosolic tRNAs. By comparison to current methods, we show that FICC-Seq is a particularly robust method for accurate and reliable detection of relevant enzymatic target sites. Our associated finding of extensive irreversible TRMT2A-tRNA crosslinking in vivo following 5-Fluorouracil exposure is also intriguing, as it suggests a tangible mechanism for a previously suspected RNA-dependent route of Fluorouracil-mediated cytotoxicity.

Indexed as

Cell SurvivalDeoxyribonucleasesFluorouracilHEK293 CellsHigh-Throughput Nucleotide SequencingHumansRNARNA, TransferSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinstRNA MethyltransferasesUridineYeastsDeoxyribonucleasesFluorouracilRNARNA, TransferSaccharomyces cerevisiae ProteinsTRM2 protein, S cerevisiaetRNA MethyltransferasesUridine

Identifiers

PMID31361898
PMCPMC6821191
OpenAlexW2964960167

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.