Evidence map›Paper›PMID 42918795›Full record

ArticleNature communications2026

The elongation of Mest transcript into MestXL sustains, but does not initiate, the maternal allele bias of its convergent gene Copg2 during neurogenesis.

Sophie Perillous, Anne-Charlotte Fromaget, Céline Gonthier-Guéret, Ornella Clerici, Marion Espenel, Alice Murigneux, Sophie Phan, Lea Feit, Catherine Vaurs-Barriére, Floric Slimani and 14 more

Abstract read
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Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Sophie Perillous *Genetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.ORCID http://orcid.org/0009-0002-3700-1720
Anne-Charlotte Fromaget *IGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.ORCID http://orcid.org/0009-0009-5953-5660
Céline Gonthier-GuéretGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-4449-559X
Ornella ClericiGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.
Marion EspenelGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.
Alice MurigneuxGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.
Sophie PhanGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.
Lea FeitGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.ORCID http://orcid.org/0009-0002-4048-8170
Catherine Vaurs-BarriéreGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0001-8654-4292
Floric SlimaniIGH, Université de Montpellier, CNRS, Montpellier, France.
Céline LemmersPlateforme de Vectorologie de Montpellier (PVM), BioCampus Montpellier, CNRS, INSERM, Université de Montpellier, Montpellier, France.
Davide NormannoIGH, Université de Montpellier, CNRS, Montpellier, France.ORCID http://orcid.org/0000-0003-4740-5542
Amanda HaDepartment of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada.
Nolan AshworthDepartment of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada.
Aaron B BogutzDepartment of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada.
Hiromi KamuraDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, Japan.
Nuttamonpat GumpangsethIGF, Univ Montpellier, CNRS, INSERM, Montpellier, France.
Kenichiro HataDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, Japan.
Bertille MontibusGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-6895-3954
Kazuhiko NakabayashiDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2927-0963
Louis LefebvreDepartment of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada.
Tristan BouschetIGF, Univ Montpellier, CNRS, INSERM, Montpellier, France. Tristan.Bouschet@igf.cnrs.fr.ORCID http://orcid.org/0000-0002-7858-6115
Franck CourtGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France. franck.court@uca.fr.ORCID http://orcid.org/0000-0003-0327-9708
Philippe ArnaudGenetics, Reproduction and Development Institute (iGReD), CNRS, INSERM, Clermont Auvergne University, Clermont-Ferrand, France. philippe.arnaud@uca.fr.ORCID http://orcid.org/0000-0002-7937-8764

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-23-CE12Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada (NSERC Canadian Network for Research and Innovation in Machining Technology) Discovery Grant (RGPIN-2024-04175).Fondation pour la Recherche Médicale (Foundation for Medical Research in France) FRM MND 2023
6 · The paper itself

Abstract

Precise gene dosage control is critical for cellular identity and development, particularly for imprinted genes, where dosage imbalances are linked to neurodevelopmental disorders. The Mest/Copg2 imprinted locus exemplifies this fine-tuned regulation: while Mest is constitutively paternally expressed, Copg2 shifts from biallelic to maternally-biased expression specifically during neural differentiation, a transition proposed to involve transcriptional interference by the long Mest isoform, MestXL, which extends into Copg2. However, the mechanisms underlying this switch and whether factors beyond MestXL contribute remain unresolved. Using a stem cell-based brain organoid model integrating multi-omic analyses, 3D chromatin mapping, and functional approaches, we challenge the prevailing model by showing that the maternal bias of Copg2 is not solely driven by MestXL-mediated interference. Instead, our data reveal a temporal, stage-specific two-step mechanism: putative enhancer-driven activation of the maternal allele in neural progenitors, followed by MestXL-dependent repression of the paternal allele in neuron-enriched stages. This uncovers an unexpected complexity in imprinted gene dosage regulation during brain development.

Indexed as

Basic Helix-Loop-Helix ProteinsNeurogenesisAllelesAnimalsBrainFemaleGene DosageGene Expression Regulation, DevelopmentalGenomic ImprintingMiceNeural Stem CellsOrganoidsBasic Helix-Loop-Helix Proteins

Identifiers

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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.