Evidence map›Paper›PMID 33035345›Full record

ArticleNucleic acids research2020

METTL3 counteracts premature aging via m6A-dependent stabilization of MIS12 mRNA.

Zeming Wu, Yue Shi, Mingming Lu, Moshi Song, Zihui Yu, Jilu Wang, Si Wang, Jie Ren, Yun-Gui Yang, Guang-Hui Liu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

117 citing papers in PubMed, 184 citations in OpenAlex.

  1. METTL14-Mediated mAging cell · 2026
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  5. Deficiency of the mCellular and molecular life sciences : CMLS · 2026
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  8. Article
  9. Review
  10. Review
  11. Article
  12. Meta-unstable mRNAs in activated CD8Nature communications · 2026
    Article
  13. Review
  14. Article
  15. Article
  16. Biomarkers of ageing of humans and non-human primates.Nature reviews. Molecular cell biology · 2025
    Review
  17. Dual roles of NScience China. Life sciences · 2025
    Article
  18. Article
  19. Article
  20. Article

57 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 1 country.

Zeming WuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Yue ShiUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Mingming LuUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Moshi SongInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Zihui YuUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Jilu WangUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Si WangInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Jie RenInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Yun-Gui YangInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Guang-Hui LiuInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Weiqi ZhangInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Weimin CiInstitute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
Jing QuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Chinese Academy of Sciences · CNCapital Medical University · CNShanghai Center For Bioinformation Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-Methyladenosine (m6A) messenger RNA methylation is a well-known epitranscriptional regulatory mechanism affecting central biological processes, but its function in human cellular senescence remains uninvestigated. Here, we found that levels of both m6A RNA methylation and the methyltransferase METTL3 were reduced in prematurely senescent human mesenchymal stem cell (hMSC) models of progeroid syndromes. Transcriptional profiling of m6A modifications further identified MIS12, for which m6A modifications were reduced in both prematurely senescent hMSCs and METTL3-deficient hMSCs. Knockout of METTL3 accelerated hMSC senescence whereas overexpression of METTL3 rescued the senescent phenotypes. Mechanistically, loss of m6A modifications accelerated the turnover and decreased the expression of MIS12 mRNA while knockout of MIS12 accelerated cellular senescence. Furthermore, m6A reader IGF2BP2 was identified as a key player in recognizing and stabilizing m6A-modified MIS12 mRNA. Taken together, we discovered that METTL3 alleviates hMSC senescence through m6A modification-dependent stabilization of the MIS12 transcript, representing a novel epitranscriptional mechanism in premature stem cell senescence.

Indexed as

AdenosineCells, CulturedCellular SenescenceHumansMesenchymal Stem CellsMethylationMethyltransferasesMicrotubule-Associated ProteinsProgeriaRNA-Binding ProteinsRNA, MessengerWerner SyndromeAdenosineIGF2BP2 protein, humanMethyltransferasesMETTL3 protein, humanMicrotubule-Associated ProteinsMIS12 protein, humanN-methyladenosineRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID33035345
PMCPMC7641765
OpenAlexW3092103071

What OpenQuestion holds

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Registered trials

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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.