Evidence map›Paper›PMID 41713742›Full record

ArticleMolecular metabolism2026

METTL18 ensures pancreatic function by maintaining proper translation and proteostasis.

Tadahiro Shimazu, Megumi Gowa, Ayane Kataoka, Takehiro Suzuki, Kotaro Tomuro, Yuichi Shichino, Naoshi Dohmae, Shintaro Iwasaki, Yoichi Shinkai

Abstract read
In one paragraph

Article in Molecular metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. METTL18 is Required for Developmental, Metabolic, and Endocrine Regulation of Mammalian Growth.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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

9 authors.

Tadahiro ShimazuCellular Memory Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan. Electronic address: tshimazu@riken.jp.
Megumi GowaCellular Memory Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan.
Ayane KataokaCellular Memory Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan.
Takehiro SuzukiBiomolecular Characterization Unit, Technology Platform Division, Center for Sustainable Resource Science, RIKEN, Wako, Saitama, 351-0198, Japan.
Kotaro TomuroRNA Systems Biochemistry Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan.
Yuichi ShichinoRNA Systems Biochemistry Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan; Department of RNA Biochemistry, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, 305-8575, Japan.
Naoshi DohmaeBiomolecular Characterization Unit, Technology Platform Division, Center for Sustainable Resource Science, RIKEN, Wako, Saitama, 351-0198, Japan.
Shintaro IwasakiRNA Systems Biochemistry Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Chiba, 277-8561, Japan.
Yoichi ShinkaiCellular Memory Laboratory, Pioneering Research Institute, RIKEN, Wako, Saitama, 351-0198, Japan. Electronic address: yshinkai@riken.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methyltransferases fine-tune various biomolecules by site-specific methylation. METTL18, an N3-position-specific histidine methyltransferase, modifies H245 of the ribosomal protein RPL3 (uL3), thereby regulating translation dynamics and proteostasis. However, the physiological role of this enzyme in vivo remains to be elucidated. Here, we show that METTL18 is essential for pancreatic function by regulating translation and suppressing protein aggregation. Mettl18 knockout (KO) mice exhibited partial preweaning lethality, and the surviving mice showed a marked reduction in N3-histidine methylation in the pancreas, diabetic phenotypes, and accumulation of pancreatitis-associated proteins. Ribosome profiling in a pancreatic acinar cell line revealed that loss of METTL18 caused global translational alterations, including accelerated elongation at proline codons. The improper ribosome traverse compromises protein folding, resulting in the aggregation of pancreatitis-associated proteins, including Reg1, and activation of the unfolded protein response. Our findings establish histidine methylation as a physiologically important post-translational modification and highlight METTL18 as a key regulator of pancreatic function through the maintenance of proteostasis.

Indexed as

MethyltransferasesPancreasProteostasisAnimalsMethylationMiceMice, KnockoutProtein BiosynthesisProtein Processing, Post-TranslationalRibosomal ProteinsRibosomesMethyltransferasesRibosomal ProteinsGlucose homeostasisHistidine methylationMETTL18Pancreatic functionRibosome functionRPL3/uL3Translation regulation

Identifiers

PMID41713742
PMCPMC12962108

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.