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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorPROUST, Carole
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDEIBER, Clémence
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMEGUERDITCHIAN, Caroline
dc.contributor.authorTUSSEAU, Maud
dc.contributor.authorGUILHEM, Alexandre
dc.contributor.authorMOHAMED, Shirine
dc.contributor.authorGOYENVALLE, Aurélie
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorJASPARD-VINASSA, Béatrice
dc.contributor.authorDUPUIS-GIROD, Sophie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorTRÉGOUËT, David-Alexandre
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorSOUKARIEH, Omar
dc.date.accessioned2025-09-01T07:30:54Z
dc.date.available2025-09-01T07:30:54Z
dc.date.issued2025-07-18
dc.identifier.issn2399-3642en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/207535
dc.description.abstractEnHereditary Hemorrhagic Telangiectasia (HHT) is a rare vascular disease mainly caused by pathogenic mutations in ACVRL1 and ENG genes. Despite advances in HHT diagnosis, the molecular origin of some cases remains unclear. Recently, we observed a high prevalence of HHT-causing 5'UTR variants in ENG. These variants commonly introduce upstream AUG codons (uAUGs) at the origin of upstream open reading frames (upORFs) overlapping the coding sequence, all terminating at the same stop codon located at position c.125 (uAUG-c.125). Here, we analyzed all 5'UTR ENG single nucleotide variants that could alter upORFs in silico. Interestingly, we found that 85% of uAUG-c.125 variants alter the protein levels. Furthermore, we identified 2 variants creating uAUG-c.125 and uCUG-c.125 in HHT patients and experimentally demonstrated their association with reduced endoglin levelsThis study provides new elements for the interpretation of upORF-altering variants in the 5'UTR of ENG with new insights for the molecular diagnosis of HHT.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enEndoglin
dc.subject.enTelangiectasia
dc.subject.enHereditary Hemorrhagic
dc.subject.enHumans
dc.subject.enOpen Reading Frames
dc.subject.en5' Untranslated Regions
dc.subject.enPolymorphism
dc.subject.enSingle Nucleotide
dc.subject.enMutation
dc.subject.enMale
dc.title.enOverlapping upstream ORFs ending at c.125 lead to reduced Endoglin, contributing to Hereditary Hemorrhagic Telangiectasia.
dc.title.alternativeCommun Biolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s42003-025-08461-6en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed40681766en_US
bordeaux.journalCommunications Biologyen_US
bordeaux.page1072en_US
bordeaux.volume8en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-05232339
hal.version1
hal.date.transferred2025-09-01T07:30:57Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Communications%20Biology&rft.date=2025-07-18&rft.volume=8&rft.issue=1&rft.spage=1072&rft.epage=1072&rft.eissn=2399-3642&rft.issn=2399-3642&rft.au=PROUST,%20Carole&DEIBER,%20Cl%C3%A9mence&MEGUERDITCHIAN,%20Caroline&TUSSEAU,%20Maud&GUILHEM,%20Alexandre&rft.genre=article


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