An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility

BACKGROUND—Genetic factors predispose to attention deficit/hyperactivity disorder (ADHD). Previous studies have reported linkage and association to ADHD of gene variants within ADGRL3. In this study, we functionally analyzed non-coding variants in this gene as likely pathological contributors. METHO...

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Tipo de recurso:
Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/26069
Acceso en línea:
https://doi.org/10.1016/j.biopsych.2016.06.026
https://repository.urosario.edu.co/handle/10336/26069
Palabra clave:
ADHD
Genetics
ADGRL3
LPHN3
Latrophilin
Cis-acting regulatory element
Enhancer
Evolutionary conserved regions
Zebrafish
Rights
License
Abierto (Texto Completo)
id EDOCUR2_d2813ab6698b97bb97bab130c0264776
oai_identifier_str oai:repository.urosario.edu.co:10336/26069
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling fc8048f6-1c84-4f79-8962-e80997a69d89-1a4dac907-d03b-422c-9a8e-bb6dd9b2d7e7-1beb39975-1be6-45be-9262-1ef99fa82133-1705ec0b7-aaaf-4fb9-b55e-d28c28ca7acf-153a3cba6-69c0-4635-bf45-18f3834cf933-1a164d108-d79b-4f13-aac2-e7f2c1fcef26-1ce0ba96b-ec3b-4bd1-9836-c3eeeef7a839-16eb93af0-3849-4536-9472-d433e00c0486-110548610-14d95c683-c5ee-4f0b-b139-77796e6c3db2-12020-08-06T16:20:35Z2020-08-06T16:20:35Z2016-12-15BACKGROUND—Genetic factors predispose to attention deficit/hyperactivity disorder (ADHD). Previous studies have reported linkage and association to ADHD of gene variants within ADGRL3. In this study, we functionally analyzed non-coding variants in this gene as likely pathological contributors. METHODS—In silico, in vitro and in vivo approaches were used to identify and characterize evolutionary conserved elements within the ADGRL3 linkage region (~207 Kb). Family-based genetic analyses on 838 individuals (372 affected and 466 unaffected) identified ADHD-associated SNPs harbored in some of these conserved elements. Luciferase assays and zebrafish GFP transgenesis tested conserved elements for transcriptional enhancer activity. Electromobility shift assays were used to verify transcription factor binding disruption by ADHD risk alleles. RESULTS—An ultraconserved element was discovered (ECR47) that functions as a transcriptional enhancer. A three-variant ADHD risk haplotype in ECR47, formed by rs17226398, rs56038622 and rs2271338, reduced enhancer activity by 40% in neuroblastoma and astrocytoma cells (PBonferroni<0.0001). This enhancer also drove GFP expression in the zebrafish brain in a tissue-specific manner, sharing aspects of endogenous ADGRL3 expression. The rs2271338 risk allele disrupts binding of YY1, an important factor in the development and function of the central nervous system. Expression quantitative trait loci analysis of post-mortem human brain tissues revealed an association between rs2271338 and reduced ADGRL3 expression in the thalamus.application/pdfhttps://doi.org/10.1016/j.biopsych.2016.06.026ISSN: 0006-3223EISSN: 1873-2402https://repository.urosario.edu.co/handle/10336/26069engSociety of Biological PsychiatryElsevier954No. 12943Biological PsychiatryVol. 80Biological Psychiatry, ISSN:0006-3223;EISSN: 1873-2402, Vol.80 No.12 (2016); pp.943–954https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108697/pdf/nihms-802870.pdfAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Biological Psychiatryinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURADHDGeneticsADGRL3LPHN3LatrophilinCis-acting regulatory elementEnhancerEvolutionary conserved regionsZebrafishAn Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibilityUn potenciador específico del cerebro ultraconservado dentro de ADGRL3 (LPHN3) apuntala la susceptibilidad al trastorno por déficit de atención / hiperactividadarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Martinez, Ariel F.Abe, YuHong, SungkookMolyneux, KevinYarnell, DavidLöhr, HeikoDriever, WolfgangAcosta, Maria T.Arcos-Burgos, MauricioMuenke, Maximilian10336/26069oai:repository.urosario.edu.co:10336/260692021-06-03 00:50:25.256https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
dc.title.TranslatedTitle.spa.fl_str_mv Un potenciador específico del cerebro ultraconservado dentro de ADGRL3 (LPHN3) apuntala la susceptibilidad al trastorno por déficit de atención / hiperactividad
title An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
spellingShingle An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
ADHD
Genetics
ADGRL3
LPHN3
Latrophilin
Cis-acting regulatory element
Enhancer
Evolutionary conserved regions
Zebrafish
title_short An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
title_full An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
title_fullStr An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
title_full_unstemmed An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
title_sort An Ultraconserved brain-specific enhancer within ADGRL3 (LPHN3) underpins attention-deficit/hyperactivity disorder susceptibility
dc.subject.keyword.spa.fl_str_mv ADHD
Genetics
ADGRL3
LPHN3
Latrophilin
Cis-acting regulatory element
Enhancer
Evolutionary conserved regions
Zebrafish
topic ADHD
Genetics
ADGRL3
LPHN3
Latrophilin
Cis-acting regulatory element
Enhancer
Evolutionary conserved regions
Zebrafish
description BACKGROUND—Genetic factors predispose to attention deficit/hyperactivity disorder (ADHD). Previous studies have reported linkage and association to ADHD of gene variants within ADGRL3. In this study, we functionally analyzed non-coding variants in this gene as likely pathological contributors. METHODS—In silico, in vitro and in vivo approaches were used to identify and characterize evolutionary conserved elements within the ADGRL3 linkage region (~207 Kb). Family-based genetic analyses on 838 individuals (372 affected and 466 unaffected) identified ADHD-associated SNPs harbored in some of these conserved elements. Luciferase assays and zebrafish GFP transgenesis tested conserved elements for transcriptional enhancer activity. Electromobility shift assays were used to verify transcription factor binding disruption by ADHD risk alleles. RESULTS—An ultraconserved element was discovered (ECR47) that functions as a transcriptional enhancer. A three-variant ADHD risk haplotype in ECR47, formed by rs17226398, rs56038622 and rs2271338, reduced enhancer activity by 40% in neuroblastoma and astrocytoma cells (PBonferroni<0.0001). This enhancer also drove GFP expression in the zebrafish brain in a tissue-specific manner, sharing aspects of endogenous ADGRL3 expression. The rs2271338 risk allele disrupts binding of YY1, an important factor in the development and function of the central nervous system. Expression quantitative trait loci analysis of post-mortem human brain tissues revealed an association between rs2271338 and reduced ADGRL3 expression in the thalamus.
publishDate 2016
dc.date.created.spa.fl_str_mv 2016-12-15
dc.date.accessioned.none.fl_str_mv 2020-08-06T16:20:35Z
dc.date.available.none.fl_str_mv 2020-08-06T16:20:35Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.biopsych.2016.06.026
dc.identifier.issn.none.fl_str_mv ISSN: 0006-3223
EISSN: 1873-2402
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/26069
url https://doi.org/10.1016/j.biopsych.2016.06.026
https://repository.urosario.edu.co/handle/10336/26069
identifier_str_mv ISSN: 0006-3223
EISSN: 1873-2402
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 954
dc.relation.citationIssue.none.fl_str_mv No. 12
dc.relation.citationStartPage.none.fl_str_mv 943
dc.relation.citationTitle.none.fl_str_mv Biological Psychiatry
dc.relation.citationVolume.none.fl_str_mv Vol. 80
dc.relation.ispartof.spa.fl_str_mv Biological Psychiatry, ISSN:0006-3223;EISSN: 1873-2402, Vol.80 No.12 (2016); pp.943–954
dc.relation.uri.spa.fl_str_mv https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108697/pdf/nihms-802870.pdf
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Society of Biological Psychiatry
Elsevier
dc.source.spa.fl_str_mv Biological Psychiatry
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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