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The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain

dc.contributor.authorPol-Fuster, Josep
dc.contributor.authorCañellas, Francesca
dc.contributor.authorRuiz-Guerra, Laura
dc.contributor.authorMedina-Dols, Aina
dc.contributor.authorBisbal-Carrio, Barbara
dc.contributor.authorOrtega-Vila, Bernat
dc.contributor.authorLlinàs, Jaume
dc.contributor.authorHernandez-Rodriguez, Jessica
dc.contributor.authorLlado, Jeronia
dc.contributor.authorOlmos, Gabriel
dc.contributor.authorStrauch, Konstantin
dc.contributor.authorHeine-Suñer, Damián
dc.contributor.authorVives-Bauza, Cristofol
dc.contributor.authorFlaquer, Antonia
dc.date.accessioned2024-09-18T06:44:12Z
dc.date.available2024-09-18T06:44:12Z
dc.date.issued2021-07-15
dc.description.abstractWe investigated the genetic causes of major mental disorders (MMDs) including schizophrenia, bipolar disorder I, major depressive disorder and attention deficit hyperactive disorder, in a large family pedigree from Alpujarras, South of Spain, a region with high prevalence of psychotic disorders. We applied a systematic genomic approach based on karyotyping (n=4), genotyping by genome-wide SNP array (n=34) and whole-genome sequencing (n=12). We performed genome-wide linkage analysis, family-based association analysis and polygenic risk score estimates. Significant linkage was obtained at chromosome 9 (9q33.1-33.2, LOD score=4.11), a suggestive region that contains five candidate genes ASTN2, BRINP1, C5, TLR4 and TRIM32, previously associated with MMDs. Comprehensive analysis associated the MMD phenotype with genes of the immune system with dual brain functions. Moreover, the psychotic phenotype was enriched for genes involved in synapsis. These results should be considered once studying the genetics of psychiatric disorders in other families, especially the ones from the same region, since founder effects may be related to the high prevalence.en
dc.description.sponsorshipThis work was supported by the Carlos III Institute of Health (ISCIII), Ministry of Economy and Competitiveness (Spain) (Grants PI15/00809 and PI18/00608), co-funded with European Union ERDF (European Regional Development Fund). JPF was funded by the FPU fellowship Granted by Ministry of Education, Culture and Sport (Spain) (FPU2014/03876). LRG, AMD and BBC were funded by the FPI fellowship granted by General Direction of Innovation and Research, Ministry of Innovation, Research and Tourism, Balearic Government (FPI/1800/2015, FPI/2059/2017, FPI/2111/2018), co-funded by European Union ERDF. KS and AF were funded by the Munich Center of Health Sciences (MC-Health), Ludwig-Maximilians-Universitat, as part of LMUinnovativ. DHS is funded by ISCIII, Ministry of Economy and Competitiveness (Spain) (Grant PI1800847), co-funded with European Union ERDF. JHR is funded by a fellowship from IDISBA (Folium Program-INTRES Project).es_ES
dc.format.number1es_ES
dc.format.page14529es_ES
dc.format.volume11es_ES
dc.identifier.citationPol-Fuster J, Canellas F, Ruiz-Guerra L, Medina-Dols A, Bisbal-Carrio B, Ortega-Vila B, et al. The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain. Sci Rep. 2021 Jul 15;11(1):14529.en
dc.identifier.doi10.1038/s41598-021-93555-4
dc.identifier.issn2045-2322
dc.identifier.journalScientific Reportses_ES
dc.identifier.otherhttps://hdl.handle.net/20.500.13003/19853
dc.identifier.pubmedID34267256es_ES
dc.identifier.puiL635631836
dc.identifier.scopus2-s2.0-85110745519
dc.identifier.urihttps://hdl.handle.net/20.500.12105/23323
dc.identifier.wos675827900028
dc.language.isoengen
dc.publisherNature Publishing Group
dc.relation.publisherversionhttps://dx.doi.org/10.1038/s41598-021-93555-4en
dc.rights.accessRightsopen accessen
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.decsProteínas de Ciclo Celular*
dc.subject.decsLigamiento Genético*
dc.subject.decsPolimorfismo de Nucleótido Simple*
dc.subject.decsFemenino*
dc.subject.decsGlicoproteínas*
dc.subject.decsMasculino*
dc.subject.decsTrastornos Psicóticos*
dc.subject.decsProteínas del Tejido Nervioso*
dc.subject.decsTrastorno por Déficit de Atención con Hiperactividad*
dc.subject.decsTrastorno Depresivo Mayor*
dc.subject.decsHumanos*
dc.subject.decsCromosomas Humanos Par 9*
dc.subject.decsLinaje*
dc.subject.decsTrastorno Bipolar*
dc.subject.decsEspaña*
dc.subject.meshDepressive Disorder, Major*
dc.subject.meshSpain*
dc.subject.meshBipolar Disorder*
dc.subject.meshChromosomes, Human, Pair 9*
dc.subject.meshNerve Tissue Proteins*
dc.subject.meshPsychotic Disorders*
dc.subject.meshHumans*
dc.subject.meshAttention Deficit Disorder with Hyperactivity*
dc.subject.meshPolymorphism, Single Nucleotide*
dc.subject.meshGlycoproteins*
dc.subject.meshMale*
dc.subject.meshFemale*
dc.subject.meshGenetic Linkage*
dc.subject.meshCell Cycle Proteins*
dc.subject.meshPedigree*
dc.titleThe conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spainen
dc.typeresearch articleen
dspace.entity.typePublication
relation.isPublisherOfPublication301fb00e-338e-4f8c-beaa-f9d8f4fefcc0
relation.isPublisherOfPublication.latestForDiscovery301fb00e-338e-4f8c-beaa-f9d8f4fefcc0

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