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dc.rights.licenseopenen_US
dc.contributor.authorVADROT, Nathalie
dc.contributor.authorADER, Flavie
dc.contributor.authorMOULIN, Maryline
dc.contributor.authorMERLANT, Marie
dc.contributor.authorCHAPON, Françoise
dc.contributor.authorGANDJBAKHCH, Estelle
dc.contributor.authorLABOMBARDA, Fabien
dc.contributor.authorMARAGNES, Pascale
hal.structure.identifierCHU Bordeaux
dc.contributor.authorRÉANT, Patricia
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorROORYCK, Caroline
dc.contributor.authorPROBST, Vincent
dc.contributor.authorDONAL, Erwan
dc.contributor.authorRICHARD, Pascale
dc.contributor.authorFERREIRO, Ana
dc.contributor.authorBUENDIA, Brigitte
dc.date.accessioned2024-02-16T08:47:31Z
dc.date.available2024-02-16T08:47:31Z
dc.date.issued2023-01-16
dc.identifier.issn2073-4409en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/188188
dc.description.abstractEnA single missense variant of the /LAP2α gene, encoding LAP2 proteins, has been associated with cardiomyopathy in two brothers. To further evaluate its role in cardiac muscle, we included in our cardiomyopathy diagnostic gene panel. A screening of ~5000 patients revealed three novel rare heterozygous variants in six males diagnosed with hypertrophic or dilated cardiomypathy. We identified in different cellular models that (1) the frameshift variant LAP2α p.(Gly395Glufs*11) induced haploinsufficiency, impeding cell proliferation and/or producing a truncated protein mislocalized in the cytoplasm; (2) the C-ter missense variant LAP2α p.(Ala240Thr) led to a reduced proximity events between LAP2α and the nucleosome binding protein HMGN5; and (3) the LEM-domain missense variant p.(Leu124Phe) decreased both associations of LAP2α/β with the chromatin-associated protein BAF and inhibition of the E2F1 transcription factor activity which is known to be dependent on Rb, partner of LAP2α. Additionally, the LAP2α expression was lower in the left ventricles of male mice compared to females. In conclusion, our study reveals distinct altered properties of LAP2 induced by these /LAP2 variants, leading to altered cell proliferation, chromatin structure or gene expression-regulation pathways, and suggests a potential sex-dependent role of LAP2 in myocardial function and disease.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enTMPO gene
dc.subject.enLAP2 proteins
dc.subject.enNuclear alterations
dc.subject.enChromatin-associated proteins
dc.subject.enE2F1 regulation
dc.subject.enGender
dc.subject.enCardiomyopathy
dc.title.enAbnormal Cellular Phenotypes Induced by Three /LAP2 Variants Identified in Men with Cardiomyopathies.
dc.title.alternativeCellsen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/cells12020337en_US
dc.subject.halSciences du Vivant [q-bio]en_US
dc.identifier.pubmed36672271en_US
bordeaux.journalCellsen_US
bordeaux.page337en_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cells&rft.date=2023-01-16&rft.volume=12&rft.issue=2&rft.spage=337&rft.epage=337&rft.eissn=2073-4409&rft.issn=2073-4409&rft.au=VADROT,%20Nathalie&ADER,%20Flavie&MOULIN,%20Maryline&MERLANT,%20Marie&CHAPON,%20Fran%C3%A7oise&rft.genre=article


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