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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

We 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...

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Autores principales: Pol-Fuster, Josep, Cañellas, Francesca, Ruiz-Guerra, Laura, Medina-Dols, Aina, Bisbal-Carrió, Bàrbara, Ortega-Vila, Bernat, Llinàs, Jaume, Hernandez-Rodriguez, Jessica, Lladó, Jerònia, Olmos, Gabriel, Strauch, Konstantin, Heine-Suñer, Damià, Vives-Bauzà, Cristòfol, Flaquer, Antònia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282839/
https://www.ncbi.nlm.nih.gov/pubmed/34267256
http://dx.doi.org/10.1038/s41598-021-93555-4
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author Pol-Fuster, Josep
Cañellas, Francesca
Ruiz-Guerra, Laura
Medina-Dols, Aina
Bisbal-Carrió, Bàrbara
Ortega-Vila, Bernat
Llinàs, Jaume
Hernandez-Rodriguez, Jessica
Lladó, Jerònia
Olmos, Gabriel
Strauch, Konstantin
Heine-Suñer, Damià
Vives-Bauzà, Cristòfol
Flaquer, Antònia
author_facet Pol-Fuster, Josep
Cañellas, Francesca
Ruiz-Guerra, Laura
Medina-Dols, Aina
Bisbal-Carrió, Bàrbara
Ortega-Vila, Bernat
Llinàs, Jaume
Hernandez-Rodriguez, Jessica
Lladó, Jerònia
Olmos, Gabriel
Strauch, Konstantin
Heine-Suñer, Damià
Vives-Bauzà, Cristòfol
Flaquer, Antònia
author_sort Pol-Fuster, Josep
collection PubMed
description We 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.
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spelling pubmed-82828392021-07-19 The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain Pol-Fuster, Josep Cañellas, Francesca Ruiz-Guerra, Laura Medina-Dols, Aina Bisbal-Carrió, Bàrbara Ortega-Vila, Bernat Llinàs, Jaume Hernandez-Rodriguez, Jessica Lladó, Jerònia Olmos, Gabriel Strauch, Konstantin Heine-Suñer, Damià Vives-Bauzà, Cristòfol Flaquer, Antònia Sci Rep Article We 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. Nature Publishing Group UK 2021-07-15 /pmc/articles/PMC8282839/ /pubmed/34267256 http://dx.doi.org/10.1038/s41598-021-93555-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pol-Fuster, Josep
Cañellas, Francesca
Ruiz-Guerra, Laura
Medina-Dols, Aina
Bisbal-Carrió, Bàrbara
Ortega-Vila, Bernat
Llinàs, Jaume
Hernandez-Rodriguez, Jessica
Lladó, Jerònia
Olmos, Gabriel
Strauch, Konstantin
Heine-Suñer, Damià
Vives-Bauzà, Cristòfol
Flaquer, Antònia
The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title_full The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title_fullStr The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title_full_unstemmed The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title_short The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
title_sort conserved astn2/brinp1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from southern spain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282839/
https://www.ncbi.nlm.nih.gov/pubmed/34267256
http://dx.doi.org/10.1038/s41598-021-93555-4
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