Evidence map›Paper›PMID 29186567›Full record

ArticleNucleic acids research2018

Dynamic m6A modification regulates local translation of mRNA in axons.

Jun Yu, Mengxian Chen, Haijiao Huang, Junda Zhu, Huixue Song, Jian Zhu, Jaewon Park, Sheng-Jian Ji

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 208 papers.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed
10.5field-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

208 citing papers in PubMed, 338 citations in OpenAlex.

  1. Review
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  5. RNA mCell biology and toxicology · 2026
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  6. Cell-Type-Specific WTAP and ALKBH5-Mediated mCNS neuroscience & therapeutics · 2026
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  8. Active transport of tRNAs facilitates distributed protein synthesis.bioRxiv : the preprint server for biology · 2026
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  9. Host mScientific reports · 2026
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  10. Integrated genetic analysis reveals synaptic mFrontiers in molecular neuroscience · 2026
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  11. Cocaine remodels mFrontiers in cellular neuroscience · 2026
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  12. Article
  13. The Role of mRNA Alternative Processing in Mammalian Neurodevelopment.International journal of molecular sciences · 2025
    Review
  14. The RNA NCell death & disease · 2025
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  15. Article
  16. Review
  17. N6-methyladenosine methylation: a novel key to unlocking mental disorders.The international journal of neuropsychopharmacology · 2025
    Review
  18. Article
  19. Article
  20. Review

148 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

8 authors at 1 institution in 2 countries.

Jun YuDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Mengxian ChenDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Haijiao HuangDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Junda ZhuDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Huixue SongDepartment of Electrical and Electronic Engineering, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Jian ZhuDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Jaewon ParkDepartment of Electrical and Electronic Engineering, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Sheng-Jian JiDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Southern University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) is a reversible modification in mRNA and has been shown to regulate processing, translation and decay of mRNA. However, the roles of m6A modification in neuronal development are still not known. Here, we found that the m6A eraser FTO is enriched in axons and can be locally translated. Axon-specific inhibition of FTO by rhein, or compartmentalized siRNA knockdown of Fto in axons led to increases of m6A levels. GAP-43 mRNA is modified by m6A and is a substrate of FTO in axons. Loss-of-function of this non-nuclear pool of FTO resulted in increased m6A modification and decreased local translation of axonal GAP-43 mRNA, which eventually repressed axon elongation. Mutation of a predicted m6A site in GAP-43 mRNA eliminated its m6A modification and exempted regulation of its local translation by axonal FTO. This work showed an example of dynamic internal m6A demethylation of non-nuclear localized mRNA by the demethylase FTO. Regulation of m6A modification of axonal mRNA by axonal FTO might be a general mechanism to control their local translation in neuronal development.

Indexed as

Protein BiosynthesisAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsAnthraquinonesAxonsEmbryo, MammalianEnzyme InhibitorsGanglia, SpinalGAP-43 ProteinMiceMice, Inbred C57BLMutationNeurogenesisRNA, MessengerRNA, Small InterferingAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnthraquinonesEnzyme InhibitorsFTO protein, mouseGAP-43 ProteinN-methyladenosinerheinRNA, MessengerRNA, Small Interfering

Identifiers

PMID29186567
PMCPMC5815124
OpenAlexW2769856951

What OpenQuestion holds

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LicenceCC BY-NC
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 OpenQuestion graph.