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dc.rights.licenseopenen_US
dc.contributor.authorRYU, Jae-Ryeon
dc.contributor.authorAHUJA, Suchit
dc.contributor.authorARNOLD, Corey R.
dc.contributor.authorPOTTS, Kyle G.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMISHRA, Aniket
dc.contributor.authorYANG, Qiong
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSARGURUPREMRAJ, Muralidharan
dc.contributor.authorMAHONEY, Douglas J.
dc.contributor.authorSESHADRI, Sudha
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDEBETTE, Stephanie
dc.contributor.authorCHILDS, Sarah J.
dc.date.accessioned2022-10-29T08:25:18Z
dc.date.available2022-10-29T08:25:18Z
dc.date.issued2022-08-30
dc.identifier.issn0027-8424 (Print)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170147
dc.description.abstractEnSNPs associated with human stroke risk have been identified in the intergenic region between Forkhead family transcription factors FOXF2 and FOXQ1, but we lack a mechanism for the association. FoxF2 is expressed in vascular mural pericytes and is important for maintaining pericyte number and stabilizing small vessels in zebrafish. The stroke-associated SNPs are located in a previously unknown transcriptional enhancer for FOXF2, functional in human cells and zebrafish. We identify critical enhancer regions for FOXF2 gene expression, including binding sites occupied by transcription factors ETS1, RBPJ, and CTCF. rs74564934, a stroke-associated SNP adjacent to the ETS1 binding site, decreases enhancer function, as does mutation of RPBJ sites. rs74564934 is significantly associated with the increased risk of any stroke, ischemic stroke, small vessel stroke, and elevated white matter hyperintensity burden in humans. Foxf2 has a conserved function cross-species and is expressed in vascular mural pericytes of the vessel wall. Thus, stroke-associated SNPs modulate enhancer activity and expression of a regulator of vascular stabilization, FOXF2, thereby modulating stroke risk.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.title.enStroke-associated intergenic variants modulate a human FOXF2 transcriptional enhancer
dc.typeArticle de revueen_US
dc.identifier.doi10.1073/pnas.2121333119en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed35994645en_US
bordeaux.journalProceedings of the National Academy of Sciences of the United States of Americaen_US
bordeaux.volume119en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue35en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamELEANOR_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03834257
hal.version1
hal.date.transferred2022-10-29T08:25:23Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20of%20the%20United%20States%20of%20America&rft.date=2022-08-30&rft.volume=119&rft.issue=35&rft.eissn=0027-8424%20(Print)&rft.issn=0027-8424%20(Print)&rft.au=RYU,%20Jae-Ryeon&AHUJA,%20Suchit&ARNOLD,%20Corey%20R.&POTTS,%20Kyle%20G.&MISHRA,%20Aniket&rft.genre=article


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