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The human 18S rRNA m6A methyltransferase METTL5 is stabilized by TRMT112

2019· article· en· 486 citations· W2962780260 on OpenAlex· 10.1093/nar/gkz619

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

No Canadian affiliation. An affiliation-only frame — the usual design — would never have seen this work. It is one of the works that make the case for inverting the frame.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Opus teacher head0.035
GPT teacher head0.364
Teacher spread
0.329 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

N6-methyladenosine (m6A) has recently been found abundantly on messenger RNA and shown to regulate most steps of mRNA metabolism. Several important m6A methyltransferases have been described functionally and structurally, but the enzymes responsible for installing one m6A residue on each subunit of human ribosomes at functionally important sites have eluded identification for over 30 years. Here, we identify METTL5 as the enzyme responsible for 18S rRNA m6A modification and confirm ZCCHC4 as the 28S rRNA modification enzyme. We show that METTL5 must form a heterodimeric complex with TRMT112, a known methyltransferase activator, to gain metabolic stability in cells. We provide the first atomic resolution structure of METTL5-TRMT112, supporting that its RNA-binding mode differs distinctly from that of other m6A RNA methyltransferases. On the basis of similarities with a DNA methyltransferase, we propose that METTL5-TRMT112 acts by extruding the adenosine to be modified from a double-stranded nucleic acid.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
Nucleic Acids Research
Topic
RNA modifications and cancer
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Funders
National Institutes of HealthCentre National de la Recherche ScientifiqueWeill Cornell Medical CollegePacific Institute for Climate SolutionsFonds De La Recherche Scientifique - FNRSDeutsche ForschungsgemeinschaftAgence Nationale de la Recherche
Keywords
BiologyMethyltransferase18S ribosomal RNAGeneticsRibosomal RNAEvolutionary biologyComputational biologyMolecular biologyDNAGeneMethylation
Has abstract in OpenAlex
yes