Evidence map›Paper›PMID 34569703›Full record

ArticleEMBO reports2021

m6A methylation promotes white-to-beige fat transition by facilitating Hif1a translation.

Ruifan Wu, Yushi Chen, Youhua Liu, Lenan Zhuang, Wei Chen, Botao Zeng, Xing Liao, Guanqun Guo, Yizhen Wang, Xinxia Wang

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 2 institutions in 1 country.

Ruifan WuCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Yushi ChenCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Youhua LiuCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Lenan ZhuangCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Wei ChenCollege of Animal Sciences, Zhejiang University, Hangzhou, China.ORCID 0000-0002-9853-8049
Botao ZengCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Xing LiaoCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Guanqun GuoCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Yizhen WangCollege of Animal Sciences, Zhejiang University, Hangzhou, China.
Xinxia WangCollege of Animal Sciences, Zhejiang University, Hangzhou, China.ORCID 0000-0002-2328-7003
Ministry of Agriculture and Rural Affairs · CNSouth China Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity mainly results from a chronic energy imbalance. Promoting browning of white adipocytes is a promising strategy to enhance energy expenditure and combat obesity. N6-methyladenosine (m6A), the most abundant mRNA modification in eukaryotes, plays an important role in regulating adipogenesis. However, whether m6A regulates white adipocyte browning was unknown. Here, we report that adipose tissue-specific deletion of Fto, an m6A demethylase, predisposes mice to prevent high-fat diet (HFD)-induced obesity by enhancing energy expenditure. Additionally, deletion of FTO in vitro promotes thermogenesis and white-to-beige adipocyte transition. Mechanistically, FTO deficiency increases the m6A level of Hif1a mRNA, which is recognized by m6A-binding protein YTHDC2, facilitating mRNA translation and increasing HIF1A protein abundance. HIF1A activates the transcription of thermogenic genes, including Ppaggc1a, Prdm16, and Pparg, thereby promoting Ucp1 expression and the browning process. Collectively, these results unveil an epigenetic mechanism by which m6A-facilitated HIF1A expression controls browning of white adipocytes and thermogenesis, providing a potential target to counteract obesity and metabolic disease.

Indexed as

Adipose Tissue, BeigeAdipose Tissue, WhiteAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsDiet, High-FatEnergy MetabolismHypoxia-Inducible Factor 1, alpha SubunitMethylationMiceMice, Inbred C57BLThermogenesisAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, mouseHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitN-methyladenosineFTOHif1am6Athermogenesistranslation

Identifiers

PMID34569703
PMCPMC8567275
OpenAlexW3203103914

What OpenQuestion holds

Textmetadata
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.