Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral pathology characterized by distinct degrees of inattention, hyperactivity and impulsivity. Although ADHD etiology remains elusive, the ADRA2A candidate gene underlies a particular interest, since it participates in the prefr...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2013
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22657
- Acceso en línea:
- https://doi.org/10.1007/s10072-013-1569-4
https://repository.urosario.edu.co/handle/10336/22657
- Palabra clave:
- Alpha 2A adrenergic receptor
Alpha 2a adrenergic receptor gene
Article
Attention deficit disorder
Child
Colombia
Controlled study
Female
Gene
Gene sequence
Genetic code
Genetic variability
Human
Major clinical study
Male
Promoter region
School child
Sequence analysis
Single nucleotide polymorphism
Wild type
Attention Deficit Disorder with Hyperactivity
Child
Colombia
Female
Humans
Male
ADHD
ADRA2A
Attention deficit hyperactivity disorder
Behavior
Genetics
Single Nucleotide
DNA
Adrenergic
alpha-2
Polymorphism
Receptors
Sequence Analysis
- Rights
- License
- Abierto (Texto Completo)
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20778e9b-ddbb-4f2f-a497-db69eb2eab8e-1f1dae9ec-4709-4f46-9cfa-032204144134-1ac5bfa62-0004-4cc0-a8b5-98ce93b8eda5-152094825600193318196004145515560079141398600797827706002020-05-25T23:57:23Z2020-05-25T23:57:23Z2013Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral pathology characterized by distinct degrees of inattention, hyperactivity and impulsivity. Although ADHD etiology remains elusive, the ADRA2A candidate gene underlies a particular interest, since it participates in the prefrontal cortex regulation of executive function. Three SNPs located on 5? and 3?UTR regions of the gene have been extensively explored but none of them have been definitely validated as a predisposition or a causative sequence variation. In this study, in order to determine whether ADRA2A non-synonymous sequence variants, resulting in biochemical modifications of the protein, are a common cause of the disease we sequenced the complete ADRA2A coding region in a panel of ADHD children of Colombian origin. We identified the c.1138 C>A (p.Arg380Arg) silent substitution. We conclude that ADRA2A non-synonymous sequence variants do not cause ADHD in our sample population. We cannot formerly discard a potential role of this gene during ADHD pathogenesis since only the coding region was analysed. We hope that these results will encourage further researchers to sequence the promoter and coding regions of ADRA2A in large panels of ADHD patients from distinct ethnical origins. © 2013 Springer-Verlag Italia.application/pdfhttps://doi.org/10.1007/s10072-013-1569-41590187415903478https://repository.urosario.edu.co/handle/10336/22657eng2222No. 122219Neurological SciencesVol. 34Neurological Sciences, ISSN:15901874, 15903478, Vol.34, No.12 (2013); pp. 2219-2222https://www.scopus.com/inward/record.uri?eid=2-s2.0-84890567991&doi=10.1007%2fs10072-013-1569-4&partnerID=40&md5=44aba97cc5c484b240337269c376d0e3Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURAlpha 2A adrenergic receptorAlpha 2a adrenergic receptor geneArticleAttention deficit disorderChildColombiaControlled studyFemaleGeneGene sequenceGenetic codeGenetic variabilityHumanMajor clinical studyMalePromoter regionSchool childSequence analysisSingle nucleotide polymorphismWild typeAttention Deficit Disorder with HyperactivityChildColombiaFemaleHumansMaleADHDADRA2AAttention deficit hyperactivity disorderBehaviorGeneticsSingle NucleotideDNAAdrenergicalpha-2PolymorphismReceptorsSequence AnalysisSequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorderarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Castro, TarynMateus, Heidi ElianaForero, DiegoFonseca Mendoza, Dora JanethRestrepo Fernández, Carlos MartínTalero Gutiérrez, ClaudiaVélez van Meerbeke, Alberto FranciscoLaissue, PaulORIGINALCastro2013_Article_SequenceAnalysisOfTheADRA2ACod.pdfapplication/pdf168956https://repository.urosario.edu.co/bitstreams/c98fd5d4-2f49-4897-8ec7-42ca54ba8011/downloadcdc4bbc49b9a4a146cfce078372c4cd8MD51TEXTCastro2013_Article_SequenceAnalysisOfTheADRA2ACod.pdf.txtCastro2013_Article_SequenceAnalysisOfTheADRA2ACod.pdf.txtExtracted texttext/plain15047https://repository.urosario.edu.co/bitstreams/394cddb7-1010-44e0-b264-32b67c370f19/download61a089a94c3ea47d878553ac8cca0db7MD52THUMBNAILCastro2013_Article_SequenceAnalysisOfTheADRA2ACod.pdf.jpgCastro2013_Article_SequenceAnalysisOfTheADRA2ACod.pdf.jpgGenerated Thumbnailimage/jpeg4806https://repository.urosario.edu.co/bitstreams/8a4feb2f-8590-480d-b42b-5ee74d6a8843/downloadc7b56599de8ad6cf6d18a2071b6defe9MD5310336/22657oai:repository.urosario.edu.co:10336/226572022-05-02 07:37:14.295133https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
title |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
spellingShingle |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder Alpha 2A adrenergic receptor Alpha 2a adrenergic receptor gene Article Attention deficit disorder Child Colombia Controlled study Female Gene Gene sequence Genetic code Genetic variability Human Major clinical study Male Promoter region School child Sequence analysis Single nucleotide polymorphism Wild type Attention Deficit Disorder with Hyperactivity Child Colombia Female Humans Male ADHD ADRA2A Attention deficit hyperactivity disorder Behavior Genetics Single Nucleotide DNA Adrenergic alpha-2 Polymorphism Receptors Sequence Analysis |
title_short |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
title_full |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
title_fullStr |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
title_full_unstemmed |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
title_sort |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder |
dc.subject.keyword.spa.fl_str_mv |
Alpha 2A adrenergic receptor Alpha 2a adrenergic receptor gene Article Attention deficit disorder Child Colombia Controlled study Female Gene Gene sequence Genetic code Genetic variability Human Major clinical study Male Promoter region School child Sequence analysis Single nucleotide polymorphism Wild type Attention Deficit Disorder with Hyperactivity Child Colombia Female Humans Male ADHD ADRA2A Attention deficit hyperactivity disorder Behavior Genetics |
topic |
Alpha 2A adrenergic receptor Alpha 2a adrenergic receptor gene Article Attention deficit disorder Child Colombia Controlled study Female Gene Gene sequence Genetic code Genetic variability Human Major clinical study Male Promoter region School child Sequence analysis Single nucleotide polymorphism Wild type Attention Deficit Disorder with Hyperactivity Child Colombia Female Humans Male ADHD ADRA2A Attention deficit hyperactivity disorder Behavior Genetics Single Nucleotide DNA Adrenergic alpha-2 Polymorphism Receptors Sequence Analysis |
dc.subject.keyword.eng.fl_str_mv |
Single Nucleotide DNA Adrenergic alpha-2 Polymorphism Receptors Sequence Analysis |
description |
Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral pathology characterized by distinct degrees of inattention, hyperactivity and impulsivity. Although ADHD etiology remains elusive, the ADRA2A candidate gene underlies a particular interest, since it participates in the prefrontal cortex regulation of executive function. Three SNPs located on 5? and 3?UTR regions of the gene have been extensively explored but none of them have been definitely validated as a predisposition or a causative sequence variation. In this study, in order to determine whether ADRA2A non-synonymous sequence variants, resulting in biochemical modifications of the protein, are a common cause of the disease we sequenced the complete ADRA2A coding region in a panel of ADHD children of Colombian origin. We identified the c.1138 C>A (p.Arg380Arg) silent substitution. We conclude that ADRA2A non-synonymous sequence variants do not cause ADHD in our sample population. We cannot formerly discard a potential role of this gene during ADHD pathogenesis since only the coding region was analysed. We hope that these results will encourage further researchers to sequence the promoter and coding regions of ADRA2A in large panels of ADHD patients from distinct ethnical origins. © 2013 Springer-Verlag Italia. |
publishDate |
2013 |
dc.date.created.spa.fl_str_mv |
2013 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:57:23Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:57:23Z |
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/10.1007/s10072-013-1569-4 |
dc.identifier.issn.none.fl_str_mv |
15901874 15903478 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22657 |
url |
https://doi.org/10.1007/s10072-013-1569-4 https://repository.urosario.edu.co/handle/10336/22657 |
identifier_str_mv |
15901874 15903478 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
2222 |
dc.relation.citationIssue.none.fl_str_mv |
No. 12 |
dc.relation.citationStartPage.none.fl_str_mv |
2219 |
dc.relation.citationTitle.none.fl_str_mv |
Neurological Sciences |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 34 |
dc.relation.ispartof.spa.fl_str_mv |
Neurological Sciences, ISSN:15901874, 15903478, Vol.34, No.12 (2013); pp. 2219-2222 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84890567991&doi=10.1007%2fs10072-013-1569-4&partnerID=40&md5=44aba97cc5c484b240337269c376d0e3 |
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