Evidence map›Paper›PMID 23144842›Full record

ArticlePloS one2012

Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta.

Anne Gabory, Laure Ferry, Isabelle Fajardy, Luc Jouneau, Jean-David Gothié, Alexandre Vigé, Cécile Fleur, Sylvain Mayeur, Catherine Gallou-Kabani, Marie-Sylvie Gross and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
12.2field-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

102 citing papers in PubMed, 196 citations in OpenAlex.

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  9. Effects of oxycodone on placental lineages: Evidence from the transcriptome profile of mouse trophoblast giant cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
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42 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

18 authors at 9 institutions in 2 countries.

Anne GaboryINRA, UMR1198 Biologie du Développement et Reproduction, Jouy-en-Josas, France.
Laure Ferry
Isabelle Fajardy
Luc Jouneau
Jean-David Gothié
Alexandre Vigé
Cécile Fleur
Sylvain Mayeur
Catherine Gallou-Kabani
Marie-Sylvie Gross
Linda Attig
Anne Vambergue
Jean Lesage
Brigitte Reusens
Didier Vieau
Claude Remacle
Jean-Philippe Jais
Claudine Junien
École Nationale Vétérinaire d'Alfort · FRUniversité de Lille · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Claude Huriez · FRHôpital Necker-Enfants Malades · FRUCLouvain · BEInserm · FRLaboratoire de Biologie du Développement · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Males and females responses to gestational overnutrition set the stage for subsequent sex-specific differences in adult onset non communicable diseases. Placenta, as a widely recognized programming agent, contibutes to the underlying processes. According to our previous findings, a high-fat diet during gestation triggers sex-specific epigenetic alterations within CpG and throughout the genome, together with the deregulation of clusters of imprinted genes. We further investigated the impact of diet and sex on placental histology, transcriptomic and epigenetic signatures in mice. Both basal gene expression and response to maternal high-fat diet were sexually dimorphic in whole placentas. Numerous genes showed sexually dimorphic expression, but only 11 genes regardless of the diet. In line with the key role of genes belonging to the sex chromosomes, 3 of these genes were Y-specific and 3 were X-specific. Amongst all the genes that were differentially expressed under a high-fat diet, only 16 genes were consistently affected in both males and females. The differences were not only quantitative but remarkably qualitative. The biological functions and networks of genes dysregulated differed markedly between the sexes. Seven genes of the epigenetic machinery were dysregulated, due to effects of diet, sex or both, including the Y- and X-linked histone demethylase paralogues Kdm5c and Kdm5d, which could mark differently male and female epigenomes. The DNA methyltransferase cofactor Dnmt3l gene expression was affected, reminiscent of our previous observation of changes in global DNA methylation. Overall, this striking sexual dimorphism of programming trajectories impose a considerable revision of the current dietary interventions protocols.

Indexed as

Epigenesis, GeneticGene ExpressionAnimalsDiet, High-FatDNA (Cytosine-5-)-MethyltransferasesFemaleGene Expression Regulation, EnzymologicHistone DemethylasesMaleMiceOligonucleotide Array Sequence AnalysisOxidoreductases, N-DemethylatingPlacentaPregnancyPrenatal Exposure Delayed EffectsPrenatal Nutritional Physiological PhenomenaDNA (Cytosine-5-)-MethyltransferasesDnmt3l protein, mouseHistone DemethylasesKdm5c protein, mouseOxidoreductases, N-Demethylating

Identifiers

PMID23144842
PMCPMC3489896
OpenAlexW2160171719

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Read underepoch 390

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.