Evidence map›Paper›PMID 40163542›Full record

ArticlePLoS biology2025

Notch3 is an asymmetric gene and a modifier of heart looping defects in Nodal mouse mutants.

Tobias Holm Bønnelykke, Marie-Amandine Chabry, Emeline Perthame, Gregor Dombrowsky, Felix Berger, Sven Dittrich, Marc-Phillip Hitz, Audrey Desgrange, Sigolène M Meilhac

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Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Science advances · 2026
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Tobias Holm BønnelykkeUniversité Paris Cité, Imagine-Institut Pasteur Unit of Heart Morphogenesis , INSERM UMR1163, Paris, France.
Marie-Amandine ChabryUniversité Paris Cité, Imagine-Institut Pasteur Unit of Heart Morphogenesis , INSERM UMR1163, Paris, France.
Emeline PerthameUniversité Paris Cité, Imagine-Institut Pasteur Unit of Heart Morphogenesis , INSERM UMR1163, Paris, France.
Gregor DombrowskyDepartment for Medical Genetics, University of Oldenburg, Oldenburg, Germany.
Felix BergerDepartment of Congenital Heart Disease, Pediatric Cardiology Deutsches Herzzentrum der Charité, Charité Universitätsmedizin Berlin, Berlin, Germany.
Sven DittrichDepartment of Pediatric Cardiology, University Hospital Erlangen, Friedrich-Alexander-University of Erlangen-Nürnberg, Erlangen, Germany.
Marc-Phillip HitzDepartment for Medical Genetics, University of Oldenburg, Oldenburg, Germany.
Audrey DesgrangeUniversité Paris Cité, Imagine-Institut Pasteur Unit of Heart Morphogenesis , INSERM UMR1163, Paris, France.
Sigolène M MeilhacUniversité Paris Cité, Imagine-Institut Pasteur Unit of Heart Morphogenesis , INSERM UMR1163, Paris, France.ORCID https://orcid.org/0000-0003-4080-2617

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TGFβ secreted factor NODAL is a major left determinant required for the asymmetric morphogenesis of visceral organs, including the heart. Yet, when this signaling is absent, shape asymmetry, for example of the embryonic heart loop, is not fully abrogated, indicating that there are other factors regulating left-right patterning. Here, we used a tailored transcriptomic approach to screen for genes asymmetrically expressed in the field of heart progenitors. We thus identify Notch3 as a novel left-enriched gene and validate, by quantitative in situ hybridization, its transient asymmetry in the lateral plate mesoderm and node crown, overlapping with Nodal. In mutant embryos, we analyzed the regulatory hierarchy and demonstrate that Nodal in the lateral plate mesoderm amplifies Notch3 asymmetric expression. The function of Notch3 was uncovered in an allelic series of mutants. In single neonate mutants, we observe that Notch3 is required with partial penetrance for ventricle thickness, septation and aortic valve, in addition to its known role in coronary arteries. In compound mutants, we reveal that Notch3 acts as a genetic modifier of heart looping direction and shape defects in Nodal mutants. Whereas Notch3 was previously mainly associated with the CADASIL syndrome, our observations in the mouse and a human cohort support a novel role in congenital heart defects and laterality defects.

Indexed as

HeartHeart Defects, CongenitalNodal ProteinReceptor, Notch3Receptors, NotchAnimalsBody PatterningGene Expression Regulation, DevelopmentalHumansMesodermMiceMutationNodal ProteinNodal protein, mouseNotch3 protein, mouseReceptor, Notch3Receptors, Notch

Identifiers

PMID40163542
PMCPMC12135939

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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.