Abstract

BackgroundFear/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.ResultsWe 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.ConclusionsWe 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.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-2936-3) contains supplementary material, which is available to authorized users.

Highlights

  • Fear/anxiety and anger/aggression greatly influence health, quality of life and social interactions

  • Our findings show that canine fear and aggression that are directed toward strange humans or other dogs share variation that was present prior to the creation of dog breeds

  • Study design The present study was designed to test whether breed stereotypes of fear and aggression could be mapped by crossbreed GWA

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Summary

Introduction

Fear/anxiety and anger/aggression greatly influence health, quality of life and social interactions. It is difficult to perform genomewide genetic association studies (GWAS) of human behavior. This is due to heterogeneity, biological complexity, ambiguous phenotype classifications and the challenges of phenotyping large numbers of individuals. Many major breakthroughs in human genetics have resulted from studying isolated populations and multigenerational families. The advantages of those latter approaches, and others, are dramatically exaggerated in dogs: (i) There are approximately 400 dog breeds, each on the order of 100-fold less genetically-complex than the full population. Examples include investigation of obsessive compulsive disorders in select breeds [10, 11] and diverse behavioral traits in one breed (nerve stability, affability, wariness, adaptability, sharpness, activity and reactions during blood drawing [12])

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