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Genetic mapping of canine fear and aggression
Open accessAbstract
BACKGROUND: Fear/anxiety and anger/aggression greatly influence health, quality of life and social interactions. They are a huge burden to wellbeing, and personal and public economics. However, while much is known about the physiology and neuroanatomy of such emotions, little is known about their genetics - most importantly, why some individuals are more susceptible to pathology under stress. RESULTS: We conducted genomewide association (GWA) mapping of breed stereotypes for many fear and aggression traits across several hundred dogs from diverse breeds. We confirmed those findings using GWA in a second cohort of partially overlapping breeds. Lastly, we used the validated loci to create a model that effectively predicted fear and aggression stereotypes in a third group of dog breeds that were not involved in the mapping studies. We found that i) known IGF1 and HMGA2 loci variants for small body size are associated with separation anxiety, touch-sensitivity, owner directed aggression and dog rivalry; and ii) two loci, between GNAT3 and CD36 on chr18, and near IGSF1 on chrX, are associated with several traits, including touch-sensitivity, non-social fear, and fear and aggression that are directed toward unfamiliar dogs and humans. All four genome loci are among the most highly evolutionarily-selected in dogs, and each of those was previously shown to be associated with morphological traits. We propose that the IGF1 and HMGA2 loci are candidates for identical variation being associated with both behavior and morphology. In contrast, we show that the GNAT3-CD36 locus has distinct variants for behavior and morphology. The chrX region is a special case due to its extensive linkage disequilibrium (LD). Our evidence strongly suggests that sociability (which we propose is associated with HS6ST2) and fear/aggression are two distinct GWA loci within this LD block on chrX, but there is almost perfect LD between the peaks for fear/aggression and animal size. CONCLUSIONS: We have mapped many canine fear and aggression traits to single haplotypes at the GNAT3-CD36 and IGSF1 loci. CD36 is widely expressed, but areas of the amygdala and hypothalamus are among the brain regions with highest enrichment; and CD36-knockout mice are known to have significantly increased anxiety and aggression. Both of the other genes have very high tissue-specificity and are very abundantly expressed in brain regions that comprise the core anatomy of fear and aggression - the amygdala to hypothalamic-pituitary-adrenal (HPA) axis. We propose that reduced-fear variants at these loci may have been involved in the domestication process.
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“Aggression and fear are associated with the same genetic loci linked to small body size, as suggested by the correlation found in Zapata et al.’s studies [162,163].”
From Ethical Concerns about Fashionable Dog Breeding (2024) · cites this paper as [162]
Experimental — accuracy not yet measuredIn the citing paper
“We noted that non-genetic models, such as stress-induced aggression [27, 81] and other organisms [30, 31, 82], were not included in this study.”
From An integrated analysis of genes and functional pathways for aggression in human and rodent models (2019) · cites this paper as [82]
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Metadata
- Authors
- Zapata, I., Serpell, J. A., & Alvarez, C. E.
- Affiliations
- Nationwide Children's Hospital (US)
- University of Pennsylvania (US)
- Corresponding author
- Alvarez, Carlos E.
- Venue
- BMC Genomics
- Published
- 2016-08-08
- Volume
- 17
- Issue
- 1
- Pages
- 572-572
- ISSN
- 1471-2164 (ISSN-L)
- PMC
- PMC4977763
- OpenAlex
- W2518047727
- Cited by
- 168
- References
- 80
- Citations by year
- 2026: 14 · 2025: 17 · 2024: 19 · 2023: 26 · 2022: 20 · 2021: 14 · 2020: 16 · 2019: 18 · 2018: 11 · 2017: 10 · 2016: 3
- FWCI
- 11.30
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Genomics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Congressionally Directed Medical Research Programs (W81XWH-11-2-0224)
- American Kennel Club Canine Health Foundation (01660)
- Morris Animal Foundation (D13CA-073)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Human-Animal Interaction Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- insulin-like growth factor I, HMGA2, IGSF1, separation anxiety, tactile sensitivity, sociability, amygdala, hypothalamic-pituitary-adrenal axis
- MeSH terms
- Aggression, Alleles, Animals, Behavior, Animal, Breeding, Chromosome Mapping, Dogs, Fear, Haplotypes, Linkage Disequilibrium, Genome, Genome-Wide Association Study, Genetic Association Studies
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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