# Metformin and Dietary Restriction Counteract Aging via Reducing m6A–Dependent Stabilization of Methionine Synthase mRNA in Brachionus asplanchnoidis (Rotifera)

**Authors:** Yu Zhang, Xiaojie Liu, Hairong Lian, Yanchao Chai, Yang Zhou, Dongqi Kan, Jilong Ren, Cui Han, Jiaxin Yang

PMC · DOI: 10.1111/acel.70113 · Aging Cell · 2025-05-27

## TL;DR

Metformin and dietary restriction extend lifespan in rotifers by reducing m6A modification of MTR mRNA, which lowers methionine levels and promotes healthy aging.

## Contribution

A novel epitranscriptional regulatory model linking m6A modification, MTR, and methionine metabolism to aging.

## Key findings

- Metformin and dietary restriction both extend rotifer lifespan by modulating m6A dynamics.
- Reduced m6A in MTR mRNA leads to lower MTR expression and decreased SAM levels.
- MTR downregulation through m6A modification promotes methionine restriction and longevity.

## Abstract

Metformin, a medication primarily used to treat diabetes, has gained attentions for its potential antiaging properties. Although the metabolic and cellular pathways behind its longevity effects have been widely studied, few studies have explored the epigenetic regulatory effects of metformin, which are a crucial factor in aging processes. In this study, we examined the antiaging effects of metformin using the Brachionus rotifer as a model, focusing on the regulation of mRNA N6–methyladenosine (m6A), a key RNA modification involved in mRNA stability, translation, and splicing. We found metformin significantly extended the rotifers' lifespan, mimicking the effects of dietary restriction (DR), a well–established antiaging intervention. Both metformin and DR modulate m6A dynamics, with a notable reduction in the m6A modification of MTR (5–methyltetrahydrofolate–homocysteine methyltransferase). This reduction led to decreased MTR expression and lowered levels of S–adenosylmethionine (SAM), a critical metabolite in the one–carbon cycle. We propose that the downregulation of MTR through m6A modification limits methionine synthesis and imposes methionine restriction, a key factor in promoting longevity. Our findings reveal a novel epitranscriptional regulatory model by which metformin and DR modulate m6A to extend lifespan, highlighting MTR as a central regulator of aging and suggesting potential therapeutic strategies for healthy aging through m6A and methionine metabolism.

Metformin and dietary restriction modulate m6A to extend lifespan of rotifer, highlighting MTR as a central regulator of aging through methionine metabolism.

## Linked entities

- **Genes:** MTR (5-methyltetrahydrofolate-homocysteine methyltransferase) [NCBI Gene 4548]
- **Chemicals:** metformin (PubChem CID 4091), S–adenosylmethionine (PubChem CID 34755), m6A (PubChem CID 102175)
- **Species:** Brachionus asplanchnoidis (taxon 1857775)

## Full-text entities

- **Genes:** MTR (5-methyltetrahydrofolate-homocysteine methyltransferase) [NCBI Gene 4548] {aka HMAG, MS, cblG}
- **Diseases:** diabetes (MESH:D003920)
- **Chemicals:** carbon (MESH:D002244), N6-methyladenosine (MESH:C010223), Metformin (MESH:D008687), S-adenosylmethionine (MESH:D012436), methionine (MESH:D008715), m6A (-)
- **Species:** Rotifera (rotifers, phylum) [taxon 10190], Brachionus asplanchnoidis (species) [taxon 1857775]

## Full text

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## Figures

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## References

127 references — full list in the complete paper: https://tomesphere.com/paper/PMC12341819/full.md

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Source: https://tomesphere.com/paper/PMC12341819