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...

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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)
id EDOCUR2_f845de2a274211c5f53b9b5f83c2acb2
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spelling 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
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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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