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ArticleClinical epigenetics2026

Neuroepigenetic programming by the maternal environment: part A-epigenome-wide DNA methylation profile in the offspring's olfactory bulb following preconceptional weight loss in mice.

Karine Badonnel, Aurélie Chaulot-Talmon, Valentin Costes, Anne Frambourg, Gabriel Costa-Monteiro-Moreira, Mélanie Jouin, Lorraine Bourgeois-Brunel, Anne Gabory, Hélène Kiefer, Hélène Jammes and 1 more

Abstract read
In one paragraph

Article in Clinical epigenetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Karine BadonnelUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France. karine.badonnel@inrae.fr.
Aurélie Chaulot-TalmonUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Valentin CostesEliance, 149 Rue de Bercy, 75012, Paris, France.
Anne FrambourgUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Gabriel Costa-Monteiro-MoreiraUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Mélanie JouinUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Lorraine Bourgeois-BrunelUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Anne GaboryUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Hélène KieferUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Hélène JammesUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France.
Christine BalyUniversité Paris-Saclay, UVSQ, INRAE, BREED, 78350, Jouy-en-Josas, France. christine.baly@inrae.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExperimental models and epidemiological data suggest that the maternal nutritional environment during gestation plays important roles in brain development with consequences on cognitive health. Epigenetic marks, such as methylation and histone modifications, are likely to be involved in this programming, but little addressed the impact of maternal metabolism at the preconceptional period. In mice, we recently demonstrated lasting effects of a maternal preconceptional weight loss on metabolic outcomes and behaviors related to food intake in the male offspring, exhibiting a reduction in olfactory sensitivity, along with a lack of fasting-induced olfactory-based motivation. To evaluate if this effect was driven by epigenetic modifications in the olfactory bulb, we profiled brain DNA methylation, a fundamental process in mediating the relation between early life environment and long-term behaviors in mice according to the maternal status.

resultsUsing oxidative reduced representation bisulfite sequencing to specifically target 5mC in mice exposed to preconceptional weight loss versus controls, we identified 11,055 differentially methylated cytosines and 150 differential methylated regions (DMRs) located in 111 genes in the olfactory bulb, a main region involved in odor processing and integration. Among the cytosines differentially methylated, half were hypermethylated. Methylation remodeling according to the maternal group preferentially affected noncoding intragenic regions, distal regulatory elements, and open sea CpGs, while promoter CpG islands remain relatively resistant to modification in DNA methylome. The functional annotation of DMRs pointed out genes related to histones kinases, energy signaling, synaptic function, and cellular differentiation, suggesting that targeted methylation changes may simultaneously influence epigenetic regulation, metabolism, and neurobiology.

conclusionThanks to a single-base analysis of differential methylated CpGs, we present novel evidence that the maternal dietary environment prior to conception exerts maternally-driven epigenetic effects, markedly altering 5-methylcytosine patterns in the adult offspring brain. This long-lasting remodeling of the offspring's olfactory bulb methylome may underlie the described alterations in olfactory-driven behaviors of offspring born to WL mother.

Indexed as

DNA MethylationOlfactory BulbWeight LossAnimalsDevelopmental Origins of Health and DiseaseEpigenesis, GeneticEpigenomeFemaleMaleMiceMice, Inbred C57BLPregnancyPrenatal Exposure Delayed EffectsBrainDOHaDEpigeneticsMethylationOlfactionoxRRBSPreconception dietWeight loss

Identifiers

PMID42897613
PMCPMC13681779

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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.