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Differential gene expression in brain tissues of aggressive and non-aggressive dogs

BACKGROUND: Canine behavioural problems, in particular aggression, are important reasons for euthanasia of otherwise healthy dogs. Aggressive behaviour in dogs also represents an animal welfare problem and a public threat. Elucidating the genetic background of adverse behaviour can provide valuable...

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Autores principales: Våge, Jørn, Bønsdorff, Tina B, Arnet, Ellen, Tverdal, Aage, Lingaas, Frode
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898780/
https://www.ncbi.nlm.nih.gov/pubmed/20553618
http://dx.doi.org/10.1186/1746-6148-6-34
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author Våge, Jørn
Bønsdorff, Tina B
Arnet, Ellen
Tverdal, Aage
Lingaas, Frode
author_facet Våge, Jørn
Bønsdorff, Tina B
Arnet, Ellen
Tverdal, Aage
Lingaas, Frode
author_sort Våge, Jørn
collection PubMed
description BACKGROUND: Canine behavioural problems, in particular aggression, are important reasons for euthanasia of otherwise healthy dogs. Aggressive behaviour in dogs also represents an animal welfare problem and a public threat. Elucidating the genetic background of adverse behaviour can provide valuable information to breeding programs and aid the development of drugs aimed at treating undesirable behaviour. With the intentions of identifying gene-specific expression in particular brain parts and comparing brains of aggressive and non-aggressive dogs, we studied amygdala, frontal cortex, hypothalamus and parietal cortex, as these tissues are reported to be involved in emotional reactions, including aggression. Based on quantitative real-time PCR (qRT-PCR) in 20 brains, obtained from 11 dogs euthanised because of aggressive behaviour and nine non-aggressive dogs, we studied expression of nine genes identified in an initial screening by subtraction hybridisation. RESULTS: This study describes differential expression of the UBE2V2 and ZNF227 genes in brains of aggressive and non-aggressive dogs. It also reports differential expression for eight of the studied genes across four different brain tissues (amygdala, frontal cortex, hypothalamus, and parietal cortex). Sex differences in transcription levels were detected for five of the nine studied genes. CONCLUSIONS: The study showed significant differences in gene expression between brain compartments for most of the investigated genes. Increased expression of two genes was associated with the aggression phenotype. Although the UBE2V2 and ZNF227 genes have no known function in regulation of aggressive behaviour, this study contributes to preliminary data of differential gene expression in the canine brain and provides new information to be further explored.
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spelling pubmed-28987802010-07-08 Differential gene expression in brain tissues of aggressive and non-aggressive dogs Våge, Jørn Bønsdorff, Tina B Arnet, Ellen Tverdal, Aage Lingaas, Frode BMC Vet Res Research article BACKGROUND: Canine behavioural problems, in particular aggression, are important reasons for euthanasia of otherwise healthy dogs. Aggressive behaviour in dogs also represents an animal welfare problem and a public threat. Elucidating the genetic background of adverse behaviour can provide valuable information to breeding programs and aid the development of drugs aimed at treating undesirable behaviour. With the intentions of identifying gene-specific expression in particular brain parts and comparing brains of aggressive and non-aggressive dogs, we studied amygdala, frontal cortex, hypothalamus and parietal cortex, as these tissues are reported to be involved in emotional reactions, including aggression. Based on quantitative real-time PCR (qRT-PCR) in 20 brains, obtained from 11 dogs euthanised because of aggressive behaviour and nine non-aggressive dogs, we studied expression of nine genes identified in an initial screening by subtraction hybridisation. RESULTS: This study describes differential expression of the UBE2V2 and ZNF227 genes in brains of aggressive and non-aggressive dogs. It also reports differential expression for eight of the studied genes across four different brain tissues (amygdala, frontal cortex, hypothalamus, and parietal cortex). Sex differences in transcription levels were detected for five of the nine studied genes. CONCLUSIONS: The study showed significant differences in gene expression between brain compartments for most of the investigated genes. Increased expression of two genes was associated with the aggression phenotype. Although the UBE2V2 and ZNF227 genes have no known function in regulation of aggressive behaviour, this study contributes to preliminary data of differential gene expression in the canine brain and provides new information to be further explored. BioMed Central 2010-06-16 /pmc/articles/PMC2898780/ /pubmed/20553618 http://dx.doi.org/10.1186/1746-6148-6-34 Text en Copyright ©2010 Våge et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Våge, Jørn
Bønsdorff, Tina B
Arnet, Ellen
Tverdal, Aage
Lingaas, Frode
Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title_full Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title_fullStr Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title_full_unstemmed Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title_short Differential gene expression in brain tissues of aggressive and non-aggressive dogs
title_sort differential gene expression in brain tissues of aggressive and non-aggressive dogs
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898780/
https://www.ncbi.nlm.nih.gov/pubmed/20553618
http://dx.doi.org/10.1186/1746-6148-6-34
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