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Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci

Anxiety disorders are among the leading health issues in human medicine. The complex phenotypic and allelic nature of these traits as well as the challenge of establishing reliable measures of the heritable component of behaviour from the associated environmental factors hampers progress in their mo...

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Autores principales: Sarviaho, R., Hakosalo, O., Tiira, K., Sulkama, S., Salmela, E., Hytönen, M. K., Sillanpää, M. J., Lohi, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336819/
https://www.ncbi.nlm.nih.gov/pubmed/30655508
http://dx.doi.org/10.1038/s41398-018-0361-x
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author Sarviaho, R.
Hakosalo, O.
Tiira, K.
Sulkama, S.
Salmela, E.
Hytönen, M. K.
Sillanpää, M. J.
Lohi, H.
author_facet Sarviaho, R.
Hakosalo, O.
Tiira, K.
Sulkama, S.
Salmela, E.
Hytönen, M. K.
Sillanpää, M. J.
Lohi, H.
author_sort Sarviaho, R.
collection PubMed
description Anxiety disorders are among the leading health issues in human medicine. The complex phenotypic and allelic nature of these traits as well as the challenge of establishing reliable measures of the heritable component of behaviour from the associated environmental factors hampers progress in their molecular aetiology. Dogs exhibit large natural variation in fearful and anxious behaviour and could facilitate progress in the molecular aetiology due to their unique genetic architecture. We have performed a genome-wide association study with a canine high-density SNP array in a cohort of 330 German Shepherds for two phenotypes, fear of loud noises (noise sensitivity) and fear of strangers or in novel situations. Genome-widely significant loci were discovered for the traits on chromosomes 20 and 7, respectively. The regions overlap human neuropsychiatric loci, including 18p11.2, with physiologically relevant candidate genes that contribute to glutamatergic and dopaminergic neurotransmission in the brain. In addition, the noise-sensitivity locus includes hearing-related candidate genes. These results indicate a genetic contribution for canine fear and suggest a shared molecular aetiology of anxiety across species. Further characterisation of the identified loci will pave the way to molecular understanding of the conditions as a prerequisite for improved therapy.
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spelling pubmed-63368192019-01-23 Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci Sarviaho, R. Hakosalo, O. Tiira, K. Sulkama, S. Salmela, E. Hytönen, M. K. Sillanpää, M. J. Lohi, H. Transl Psychiatry Article Anxiety disorders are among the leading health issues in human medicine. The complex phenotypic and allelic nature of these traits as well as the challenge of establishing reliable measures of the heritable component of behaviour from the associated environmental factors hampers progress in their molecular aetiology. Dogs exhibit large natural variation in fearful and anxious behaviour and could facilitate progress in the molecular aetiology due to their unique genetic architecture. We have performed a genome-wide association study with a canine high-density SNP array in a cohort of 330 German Shepherds for two phenotypes, fear of loud noises (noise sensitivity) and fear of strangers or in novel situations. Genome-widely significant loci were discovered for the traits on chromosomes 20 and 7, respectively. The regions overlap human neuropsychiatric loci, including 18p11.2, with physiologically relevant candidate genes that contribute to glutamatergic and dopaminergic neurotransmission in the brain. In addition, the noise-sensitivity locus includes hearing-related candidate genes. These results indicate a genetic contribution for canine fear and suggest a shared molecular aetiology of anxiety across species. Further characterisation of the identified loci will pave the way to molecular understanding of the conditions as a prerequisite for improved therapy. Nature Publishing Group UK 2019-01-17 /pmc/articles/PMC6336819/ /pubmed/30655508 http://dx.doi.org/10.1038/s41398-018-0361-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sarviaho, R.
Hakosalo, O.
Tiira, K.
Sulkama, S.
Salmela, E.
Hytönen, M. K.
Sillanpää, M. J.
Lohi, H.
Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title_full Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title_fullStr Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title_full_unstemmed Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title_short Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
title_sort two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336819/
https://www.ncbi.nlm.nih.gov/pubmed/30655508
http://dx.doi.org/10.1038/s41398-018-0361-x
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