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...
- Autores:
- 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)
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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 |
_version_ |
1814167499069980672 |