Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/142544
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dc.creatorDarrigrand, JF
dc.creatorValente, M
dc.creatorComai, G
dc.creatorMartinez, P
dc.creatorPetit, M
dc.creatorNishinakamura, R
dc.creatorOsório, DS
dc.creatorRenault, G
dc.creatorMarchiol, C
dc.creatorRibes, V
dc.creatorCadot, B
dc.date.accessioned2022-08-01T11:22:51Z-
dc.date.available2022-08-01T11:22:51Z-
dc.date.issued2020
dc.identifier.issn2050-084X
dc.identifier.urihttps://hdl.handle.net/10216/142544-
dc.description.abstractThe establishment of separated pulmonary and systemic circulation in vertebrates, via the cardiac outflow tract (OFT) septation is a sensitive developmental process accounting for 10% of all congenital anomalies. Neural Crest Cells (NCC) colonising the heart condensate along the primitive endocardial tube and force its scission into two tubes. Here, we show that NCC aggregation progressively decreases along the OFT distal-proximal axis following a BMP signalling gradient. Dullard, a nuclear phosphatase, tunes the BMP gradient amplitude and prevents NCC premature condensation. Dullard maintains transcriptional programs providing NCC with mesenchymal traits. It attenuates the expression of the aggregation factor Sema3c and conversely promotes that of the epithelial-mesenchymal transition driver Twist1. Altogether, Dullard-mediated fine-tuning of BMP signalling ensures the timed and progressive zipper-like closure of the OFT by the NCC and prevents the formation of an heart carrying the four congenital abnormalities defining the tetralogy of Fallot.
dc.description.sponsorshipAgence Nationale de la Re-cherche - ANR-14-CE09-0006-04 Bruno Cadot; Ligue Contre le Cancer PREAC2016.LCC Vanessa Ribes - Agence Nationale de la Re-cherche; ANR-10-LABX-73 Mariana Valente. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
dc.language.isoeng
dc.publishereLife Sciences Publications
dc.relation.ispartofeLife, vol.9:e50325
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.meshAnimals
dc.subject.meshGene Deletion
dc.subject.meshGene Expression Regulation, Developmental
dc.subject.meshHeart / embryology
dc.subject.meshMice
dc.subject.meshMyocardium / cytology
dc.subject.meshMyocardium / metabolism
dc.subject.meshNeural Crest / cytology
dc.subject.meshPhosphoprotein Phosphatases / genetics
dc.subject.meshPhosphoprotein Phosphatases / physiology
dc.subject.meshSignal Transduction
dc.subject.meshSmad1 Protein / genetics
dc.subject.meshSmad1 Protein / metabolism
dc.subject.meshSmad5 Protein / genetics
dc.subject.meshSmad5 Protein / metabolism
dc.subject.meshSmad8 Protein / genetics
dc.subject.meshSmad8 Protein / metabolism
dc.subject.meshTetralogy of Fallot / prevention & control
dc.titleDullard-mediated smad1/5/8 inhibition controls mouse cardiac neural crest cells condensation and outflow tract septation
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.7554/eLife.50325
dc.relation.publisherversionhttps://elifesciences.org/articles/50325
Appears in Collections:ICBAS - Artigo em Revista Científica Internacional

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