Evidence map›Paper›PMID 40524957›Full record

ArticleiScience2025

Acute dietary methionine restriction triggers cell cycle arrest and reversible growth defects in the neocortex.

Sulov Saha, Clémence Debacq, Christophe Audouard, Thomas Jungas, Pierrick Dupré, Fawal Mohamad-Ali, Clément Chapat, Henri-Alexandre Michaud, Laurent Le Cam, Matthieu Lacroix and 2 more

Abstract read
In one paragraph

Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

12 authors.

Sulov SahaMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Clémence DebacqMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Christophe AudouardMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Thomas JungasMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Pierrick DupréInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université de Montpellier, Institut Régional du Cancer de Montpellier (ICM), 34298 Montpellier, France.
Fawal Mohamad-AliMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Clément ChapatMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Henri-Alexandre MichaudInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université de Montpellier, Institut Régional du Cancer de Montpellier (ICM), 34298 Montpellier, France.
Laurent Le CamInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université de Montpellier, Institut Régional du Cancer de Montpellier (ICM), 34298 Montpellier, France.
Matthieu LacroixInstitut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Université de Montpellier, Institut Régional du Cancer de Montpellier (ICM), 34298 Montpellier, France.
David OhayonMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.
Alice DavyMolecular, Cellular and Developmental Biology Unit, MCD-CBI, Université de Toulouse, CNRS, 118 Route de Narbonne 31062 Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methionine is indispensable for cell proliferation, stem cell maintenance, and epigenetic regulation, three processes that are central to embryonic development. Here, we assessed the consequences of short-term dietary methionine restriction (MR) on mouse embryonic organ growth. In comparison with growth of the liver and heart which was unaffected, MR for 5 days led to a severe reduction in neuronal production and neocortex growth. Progenitor cohort labeling revealed a time-dependent sensitivity to MR and cell cycle analysis indicated that progenitors are stalled in S/G2 phases following MR. Unexpectedly, neuronal production was completely rescued at birth when switching the dam back to control diet, uncovering a mechanism of catch-up growth. We used imaging mass cytometry to probe metabolic and epigenetic markers in neural progenitors following MR and during catch-up growth. Altogether, our data uncover a reversible state of quiescence in S/G2 which is metabolically distinct from G0 quiescence and associated with efficient catch-up growth of the neocortex.

Indexed as

Molecular biologyNeuroscience

Identifiers

PMID40524957
PMCPMC12167773

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.