Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies

Summary

Domestic dogs can suffer from hearing losses that can have profound impacts on working ability and quality of life. We have identified a type of adult-onset hearing loss in Border Collies that appears to have a genetic cause, with an earlier age of onset (3–5 years) than typically expected for aging dogs (8–10 years). Studying this complex trait within pure breeds of dog may greatly increase our ability to identify genomic regions associated with risk of hearing impairment in dogs and in humans. We performed a genome-wide association study (GWAS) to detect loci underlying adult-onset deafness in a sample of 20 affected and 28 control Border Collies. We identified a region on canine chromosome 6 that demonstrates extended support for association surrounding SNP Chr6.25819273 (p-value = 1.09×10⁻¹³). To further localize disease-associated variants, targeted next-generation sequencing (NGS) of one affected and two unaffected dogs was performed. Through additional validation based on targeted genotyping of additional cases (n = 23 total) and controls (n = 101 total) and an independent replication cohort of 16 cases and 265 controls, we identified variants in USP31 that were strongly associated with adult-onset deafness in Border Collies, suggesting the involvement of the NF-κB pathway. We found additional support for involvement of RBBP6, which is critical for cochlear development. These findings highlight the utility of GWAS–guided fine-mapping of genetic loci using targeted NGS to study hereditary disorders of the domestic dog that may be analogous to human disorders.

Introduction

Age-related hearing loss (presbycusis) occurs in humans with a prevalence of about 40% in individuals older than 65 years of age. It is associated with difficulties of communication, isolation, depression and possibly even dementia in the severely affected [1]. There are extensive genetic contributions to hearing variation [2], which has an estimated heritability of 35–55% (reviewed in [3]). Studies in humans have identified risk-conferring variants in both mitochondrial [4], [5] and autosomal DNA (reviewed in [3]). A recent genome-wide association study (GWAS) performed in an isolated Finnish population identified the candidate gene IQ motif containing GTPase activating protein 2 (IQGAP2) as a novel risk locus for hearing loss [6], as well as modest support for another, previously identified GWAS candidate, metabotropic glutamate receptor 7 (GRM7) [7]. Overall, however, the breadth of genetic variation that may confer risk for this common disorder remains unknown.

The domestic dog offers a unique opportunity to explore the genetic backgrounds of naturally occurring disorders that are analogous to human diseases. Genomic studies are particularly informative when a disorder of interest demonstrates a simpler inheritance pattern in dogs than in humans, suggesting one or a few main risk alleles. Deterioration of hearing with age is normal in dogs, with an onset at 8–10 years [8] that corresponds with physiological changes in critical systems in the ear, including reduced spiral ganglion neuronal density in the cochlea [9]. Shimada et al. [10] reported that dogs with hearing loss demonstrated the same four types of lesions found in humans (as described by Schuknecht & Gacek [11]): sensory, neural, strial and cochlear conductive lesions. Physiological measurements of hearing ability using brainstem auditory evoked response (BAER) demonstrate similar patterns in dogs and humans, with high- and mid-range frequencies being the most severely affected [8], [12]. Thus, age-related hearing loss may be similar in both clinical presentation and underlying pathology in humans and dogs.

Across breeds, presbycusis is estimated to begin at 8–10 years, when deterioration is observed at all frequencies [8]. However, adult-onset deafness in Border Collies often has an earlier onset (3–5 years) than deafness resulting from the physiological aging of hearing organs. Distinct from other breeds, the Border Collie has been selected for over 100 years to perceive and respond to whistle commands while working at distances of 800 meters or more from a handler. Being able to detect slight differences in whistle tones is essential to the function of a working Border Collie, and even moderate hearing loss in one ear can have a major impact on working ability. Although relatively uncommon in Border Collies, adult-onset deafness is considered especially problematic because hearing is so integral to the tasks for which these dogs are selectively bred and used. In addition, dogs afflicted by adult-onset deafness are often in their prime working years, with the average age of top working dogs around 7 years [13].

The earlier age of onset in affected Border Collies suggests that adult-onset deafness is genetically influenced and possibly more severe than that observed in other breeds of dogs. Many of the affected dogs included in this study were reported by their owners to have one or more first-degree family members with similar deafness. We undertook a study to identify genetic risk factors and address concerns regarding adult-onset deafness among Border Collies, as well as potentially gain information about analogous human conditions.

Results

Adult-Onset Deafness in Border Collies

The exact age of onset of hearing deterioration is often difficult to ascertain in pet dogs, because subtle changes may go unnoticed by pet owners and because dogs are known to compensate for hearing loss [14]. However, the owners of the dogs included in this study estimated the age of onset of hearing loss based upon close observations of behavioral characteristics in working dogs indicating poor hearing (e.g., reduced call distance, poor performance). The average estimated age of onset was 4.3 years (S.E. of 0.5 years), with a range of 1–9 years.

Genome-Wide Association Study

A total of 48 unrelated Border Collies (20 cases, 28 controls) were utilized for the primary association study (Table S1). Following quality control of the genotype data, 30,231 SNPs were retained for genetic mapping. Genome-wide association analyses with EMMAX identified a region on CFA6, at approximately 25 Mb (Figure 1). In total, 25 markers exhibited significance beyond a Bonferroni-corrected threshold (p = 1.65×10⁻⁶ for 30,231 tests). The strongest finding was an intergenic SNP, Chr6.25819273, with a p-value of 1.09×10⁻¹³ (Table 1), with strong regional support demonstrated by neighboring SNPs whereby, within 1 Mb flanking the top finding, six reached Bonferroni significance. The closest predicted gene to this SNP is HS3ST2, approximately 24 kb downstream of the marker. HS3ST2 is a member of the heparan sulfate biosynthetic enzyme family, and is expressed predominantly in the brain [15].

Associations were also assessed through permutation analysis in PLINK. One million permutations yielded genome-wide permutated p-values that achieved genome-wide significance (Table 1). Analyses of copy number variation using genome-wide SNP data did not reveal evidence of structural changes associated with hearing loss. Association modeling suggested an autosomal recessive mode of inheritance for adult-onset deafness in Border Collies.

Fine-Mapping

The large candidate region identified on CFA 6 was syntenic with human 16p12.1-p12.3, which encompasses the human autosomal recessive deafness locus DFNB22 [16]. A candidate of immediate interest within this region was the gene OTOA, defects of which were implicated in a case of prelingual sensorineural deafness in a consanguineous Palestinian family [16]. We performed PCR amplifications of the 28 exons and a highly conserved non-coding region. PCR products were sequenced and analyzed for mutations in affected dogs. None of the observed polymorphisms tracked specifically in affected dogs.

Given the large region of association and lack of polymorphisms in the strong candidate gene OTOA, we next narrowed the critical region for the 25-Mb locus by haplotype analysis. We detected a 7-SNP haplotype that was homozygous in all cases but only once among the control samples (see Discussion). A larger 11-SNP haplotype was found homozygous in 19 of 20 cases and present in the same control. (Figure 2). For sequencing via target capture and next-generation sequencing (NGS), we selected an affected dog that was homozygous for the extended 11-SNP risk haplotype at 25 Mb (Figure 2). Two control dogs that did not carry the candidate risk haplotype were also sequenced after target capture by NGS.

The risk haplotype spanning the coordinates on CFA6 from 25.5–25.9 Mb was used to guide mutation discovery with the NGS data. We identified predicted genes based on synteny and the annotated gene index, and designed a solution-based target capture mixture to target exons and introns, along with at least 1 kb of upstream and downstream regions possibly inclusive of UTR sequence. This capture design encompassed 2.3 Mb, and included 73 genes. NGS rendered over 30 million reads per sample (Table S2). More than 90% of these reads could be aligned to the reference genome sequence (CanFam2). Of the total targeted sequence, 75% had greater than 10× coverage, and nearly 70% had >30× coverage (Table S7).

The numbers and types of variants identified are summarized in Table S3. One strong non-synonymous SNP (nsSNP) candidate, Chr6.25714052, is located in exon 17 of USP31, which encodes an ubiquitin specific peptidase. It is an A>G variant that is predicted to cause an I847V change in the resulting protein product. The position is highly conserved, with a phastCons score of 0.95 (Table S4), although SIFT predicted the change to be tolerated (SIFT score of 0.66). Also of note in USP31 is an intronic T>G SNP (Chr6.25681850) that is very highly conserved (phastCons score of 0.98) and is 5 bp away from an intron-exon boundary. This variant was called G/G in the case and T/T in both controls. Both variants are located within the risk haplotype.

Another candidate nsSNP, Chr6.24500625, is in exon 18 of RBBP6, encoding a retinoblastoma binding protein. This nsSNP changes threonine to asparagine at residue 1,397. This G>T variant was called T/T in the case and G/G in both controls. SIFT predicted the change to be tolerated (SIFT score = 0.69; Table S4). Although the conservation score for this SNP is low (phastCons = 0.001) and the variant is located upstream of the main risk haplotype, RBBP6 (also known as PACT) plays a critical role in ear development and hearing; disruption of the gene has been shown to cause congenital hearing impairment in mice [17] and suggests high relevance to hearing loss in dogs. The sequencing data from 25 Mb did not exhibit variants in OTOA that were homozygous in the case but not in controls. Therefore, we did not consider this to be the causative gene. Although small insertion/deletion variants were found in the mapped intervals, none of these variants appeared to be causal.

The three variants described above, Chr6.24500625 in RBBP6, and Chr6.25681850 and Chr6.25714052 in USP31, were the most compelling for follow-up genotyping analyses due to biological implications (RBBP6) and location within the risk haplotype (USP31), and were analyzed both for validation (primary mapping cohort) and replication (independent cases and controls).

Validation

Genotyping was performed via dye-terminator sequencing for the three chosen variants. All three showed associations with adult-onset deafness (Table 2). For replication analysis, we genotyped an independent Border Collie cohort of 16 cases and 265 controls. All three SNPs were strongly associated with adult-onset deafness (Table 2), replicating our previous mapping results. Meta-analysis of the combined primary and replication cohorts yielded even stronger associations for all three variants. The strongest association was found for the variant of USP31, Chr6.25681850, with p = 6.16×10⁻²² (Table 2).

Discussion

Our results represent the first GWAS of adult-onset deafness in the domestic dog. We demonstrated the successful application of target capture for next-generation sequencing (NGS) in the dog. The region implicated by GWAS in our study is syntenic to regions implicated in congenital sensorineural deafness in humans.

In this study, we identified three strong candidate coding and non-coding variants associated with adult-onset deafness. The strongest is Chr6.25681850, an intronic SNP in USP31 that is 5 bp from an intron-exon boundary and may play a role in alternate splicing (as annotated in humans). Preliminary studies of mRNA collected from peripheral blood samples from two dogs harboring this variant did not suggest changes in RNA splicing in this region, though tissue-specific changes in RNA regulation cannot be ruled out. USP31 is a ubiquitin-related gene that has been linked to Parkinson's disease in humans [18]. The implication of a ubiquitin-related gene in adult-onset deafness is particularly intriguing given the histological findings of Shimada et al. [10], which included ubiquitin-positive granules in the neuropil of cochlear nuclei of aging dogs. USP31 has also been shown to regulate NF-κB activation; NF-κB deficiency is associated with increased levels of cochlear apoptosis and hearing loss [19], [20]. Despite its location outside the main risk haplotype implicated in the primary GWAS, the second-strongest association was the nsSNP Chr6.24500625, which is exonic to RBBP6, a gene previously implicated in hearing in a knockout mouse model [17]. In addition to roles in development, RBBP6 may also be involved in chaperone-mediated ubiquitination and protein quality control [21], suggesting another potential role in pathology. A second USP31 SNP, Chr6.25714052, was also associated with adult-onset deafness in our cohort, although this locus had the lowest odds ratio of the three candidate loci.

There are several caveats to the present study. A recent human GWAS for presbycusis adjusted phenotypes for hearing thresholds according to age and sex, due to observed variability in hearing threshold in males and females [6]. We elected not to correct for sex in our canine study because such sexual dimorphism is not yet established in aging dogs [8], [10], [12], [14]. Further, we did not adjust for age because the age of onset for our sample cohort, which is likely a specific trait of this form of hearing loss, was owner-estimated. The mean age of our control group was 6.6 years, which is close to the range of hearing loss onset. Therefore, it is possible that dogs categorized as “controls” may, at later stages in life, demonstrate hearing loss similar to that observed in cases. For example, one interesting case involves a dog that was classified as a control at the time of collection (41 months old) and was shown to carry the 11-SNP risk haplotype we identified in affected dogs (this dog is indicated by the asterisk in Figure 2). This dog was later found to have several deaf siblings. In the follow-up SNP genotyping cohort, several Finnish dogs classified as controls by owner questionnaires were also found to carry one or more of the risk alleles identified during NGS (Table 2). Two of these dogs were later found to have had changes in hearing since initial sample collection, and further inquiry uncovered additional family histories of hearing loss in both dogs' pedigrees. However, the misclassification of cases as controls would only reduce analytical power to detect genetic associations, and would not result in spurious associations. Given the strengths of the associations we identified on CFA6, this does not seem to be a concern. Similarly, the presence of the risk haplotype in the homozygous state in all cases suggests that we are not detecting phenotypic heterogeneity influenced by another locus, such as occult congenital unilateral pigmentation-related forms of deafness.

Another caveat stems from the fact that we performed target enrichment for selected regions (i.e., all predicted genes) of extended association loci, and therefore non-coding variants far outside of known or predicted genes were potentially missed. Target enrichment results in uneven coverage, so variants may be missed because not all positions are covered equally well, although the regions that were captured appear to be well assembled (Figures S3, S4; Table S6). Finally, the magnitude of our findings on CFA6 in the primary GWAS (Figure S2) likely overshadowed signals from other regions, even if modifying loci were present.

A strength of canine research highlighted by this study is the reliability of owners to assess phenotype. Each case in the GWAS for adult onset hearing loss was scored by the owner. The results of mapping showed that every case was homozygous for an ancestral risk haplotype, providing compelling support of the initial owner assessment. We view this as tapping the same insights gained by a parent, who develops an intimate awareness of their child's health and behavior. Our results have implications for researchers interested in other canine behavioral traits, in that owner-based observation may be sufficient, at least initially, to advance genetic studies.

Although we observed robust associations and replications, none of the candidate SNPs we identified tracked perfectly with adult-onset deafness. This discrepancy has several possible explanations: 1) adult-onset deafness in the Border Collie is a multigenic trait, 2) the risk locus shows incomplete penetrance, or 3) the variants we identified are in linkage disequilibrium with the true disease-causing mutation. The fact that the RBBP6 SNP demonstrated a stronger association than the second USP31 SNP, Chr6.25714052, likely reflects extended linkage in cases that was not readily apparent in haplotype analyses, and may provide information regarding the location of the true causative variant. Given that the 7-SNP homozygous haplotype is present in all cases, it is likely that the variants we identified, which do not track perfectly with larger samples of cases, are more recent in origin than the common tagging SNPs utilized in array genotyping. This would suggest that the causative variant has occurred within the context of a broader, ancestral haplotype. The causative mutation for adult-onset deafness may be a non-coding variant between Chr6.24500625 and Chr6.25681850 that was not captured during target enrichment, and structural variation may also be missed with this technology. Numerous mapping studies in the dog have identified structural variants as causative mutations of traits or disorders [22].

The risk allele of the most strongly-associated SNP from NGS exhibited a frequency of 0.23–0.31 in our Border Collie control sample (Table 2). Future studies may clarify whether this risk allele occurs at similar frequencies in other breeds of dog. Alternative mapping strategies utilizing highly polymorphic microsatellite markers in haplotypes and including different breeds of dog may allow for more refined mapping of structural variants underlying adult-onset deafness. In light of our strong genetic findings, longitudinal studies of dogs that carry risk alleles are warranted for further phenotypic characterization, including histopathologic examination of the middle ears and cochlea. Such investigations may allow us to further characterize and explore the hypothesis that these animals are affected by pure sensorineural deafness, as demonstrated by BAER testing. Observations of the effects of risk variants on aspects of hearing throughout the aging process could provide critical prognostic information for the development of diagnostic or therapeutic tools for use in clinical contexts in both dogs and in humans. It is possible that hearing loss is identified earlier by handlers of dogs for which working ability depends strongly on hearing acuity, such as working Border Collies. Physiological findings may thus be particularly relevant to studies of other utility-bred dogs, in addition to studies of hearing loss that naturally occurs in geriatric dogs.

In conclusion, we identified candidate variants on CFA6 that are strongly associated with adult-onset deafness in Border Collies, with promising implications for future pre-morbid identification of at-risk dogs or applications to human studies. Preliminary causative variant fine-mapping analyses indicate that variants in USP31 and RBBP6 may be involved in disease etiology. Future studies to elucidate the roles of these variants in canine adult-onset hearing loss will include haplotype mapping for the detection of structural variations and longitudinal studies of gene effects on hearing electrophysiology trajectories and outcomes.

Materials and Methods

Ethics Statement

All work related to animals was performed with the approval of the Institutional Animal Care and Use Program at the University of California, San Francisco (AN079848-02). Collection of blood samples in Finland was approved by the Animal Ethics Committee at the State Provincial Office of Southern Finland (ESLH-2009-07827/Ym-23). The canine samples used were provided by private dog owners, who consented to the use of de-identified data for research purposes.

Samples

Whole blood samples (3–8 mL) from a total of 48 purebred Border Collies collected in the United States (U.S.) were used for primary GWAS. Samples from 20 affected working Border Collies recruited from owners from the sheepdog/herding community were collected specifically for this genetic survey of risk loci for adult-onset deafness. Twenty-eight control samples (unrelated at the grandparental level, per pedigree analysis) were collected at sheepdog trials or sent directly to the laboratory by owners and breeders in the context of ongoing genetic studies of canine behavior and complex disease. The 20 adult-onset deafness cases included 9 males and 11 females, and the 28 controls included 15 males and 13 females (mean age of controls, 6.6 years). One of the cases and two controls were also sequenced using next-generation sequencing (NGS) technology. An additional 14 U.S. controls and 3 cases and 59 controls collected in Finland were used for follow-up genotyping of candidate variants. Finally, samples from 16 cases and 265 controls were also collected in the U.S. to serve as an independent replication cohort. All follow-up and replication samples were from purebred Border Collies. Although consisting primarily of distinct breeding lines, the Finnish dogs demonstrated similar allele frequencies for the genotyped variants as the U.S. dogs, and thus both groups were analyzed together. The use of a covariate to account for difference in country of origin/breeding line did not change the results of association analysis. DNA was extracted using standard protocols. A summary of the samples is provided in Table S1.

Phenotypes

Adult-onset deafness phenotypes were assigned based on owner responses to verbal questions to determine whether or not a sampled dog exhibited hearing loss that had developed in adulthood (i.e., deafness that was not congenital). Hearing loss was determined indirectly by owner observations of working dogs that were previously responsive to verbal and whistle commands given in both home and working conditions, but as adults demonstrated significant decreases in response or apparent inability to hear commands. Such loss of hearing was often observed to take place over the course of several months or years. Some owners said that they did not notice any significant changes in their dogs' hearing ability until much later in the dogs' lives, but they suspected that the dog was “compensating” in the work environment by observing the handlers' physical cues or by moving closer to the handler when commands were being given. Controls for the primary GWAS portion of the study were herding Border Collies that met two criteria: 1) genetic clustering in the same group as affected dogs (genetic matching), and 2) no hearing loss indicated in the health sections of behavioral questionnaires completed by owners at the time of sample collection. For follow-up and replication genotyping, U.S. cases were identified as above and controls were defined as dogs that displayed no hearing loss as indicated by owners at the time of sample collection. For all Finnish dogs, deafness phenotypes were obtained through owner interviews via questionnaires.

Genome-Wide Genotyping

SNP genotyping was performed on the Affymetrix Custom Canine Array v2.0 according to the manufacturer's protocol, a perfect-match-only array targeting 127,000 SNPs (Affymetrix, Santa Clara, CA, USA). Genotypes were called using the BRLMM-P algorithm in Affymetrix Power Tools (apt-1.12.0). Genotype quality control (QC) was first implemented for all of the samples we genotyped on the Affymetrix array for ongoing studies of complex disease (n = 275), which included unrelated dogs as well as a subset of related dogs to assess Mendelian errors. SNP exclusion criteria for the full set were call rates by marker and by individual<95%; concordance of replicate control sample genotypes across all genotyping runs<100%; X-chromosome markers; deviations from Hardy-Weinberg equilibrium with p-values<0.001; minor allele frequency<0.02; and Mendelian errors>5% per SNP. This filtering resulted in a primary dataset of about 40,000 SNPs. After additional QC on only the 48 unrelated samples included in the GWAS for adult-onset deafness (exclusions: SNP call rate<95%, MAF<0.05), approximately 30,000 SNPs were retained for final analysis. QC was performed using Stata10/MP (StataCorp LP, College Station, TX, USA) and PLINK (v1.06–1.07 [23]).

Target Capture and Next-Generation Sequencing

Genomic library sample preparation was performed using the Illumina single-end library sample preparation kit (Illumina Inc., San Diego, CA, USA). Sample preparation was carried out according to the manufacturer's instructions, except for slight modifications as follows: 3 µg of genomic DNA were sheared via sonication (S-4000 with 2.5″ diameter cup horn, Misonix, Inc., Farmingdale, NY, USA); all purification steps were performed using Agencourt AMPure XP magnetic beads (Beckman Coulter, Inc., Brea, CA, USA); seven cycles of ligation-mediated PCR were used for library amplification. Sample libraries were run on a Bioanalyzer 2100 for DNA quantitation and confirmation of fragment size distribution (High Sensitivity DNA Kit, Agilent Technologies, Waldbronn, Germany). For targeted sequencing, we performed solution-based capture with the Agilent SureSelect Target Enrichment System Kit. Briefly, a custom panel of 120-base cRNA oligos was designed to target 1000 bp upstream and downstream of 73 predicted gene sequences based on mammalian alignments (or in one case, frog) to CanFam2 in the candidate region on CFA6 (Table S6). The target regions were covered by approximately 43,000 probes that were designed for 3× coverage (i.e., each base was covered by three different probes). The prepared genomic libraries were hybridized to the panel of biotin-labeled “bait” oligos for 24 hours. Targets were pulled down via streptavidin magnetic beads, purified, and enriched through 13 cycles of PCR amplification. Samples were single-end sequenced on an Illumina Genome Analyzer IIx for 76 cycles.

Dye-Terminator Sequencing

Three variants were selected for genotyping via dye-terminator sequencing. All samples included in the study were sequenced. A PCR amplicon was designed for each region, and sequencing was performed in the forward and reverse directions (primer sequences provided in Table S5). We used 1 µL of 1 ng/µL of DNA as input for each standard PCR reaction. Platinum-Taq polymerase was used to amplify segments with a 58°C touchdown protocol in the presence of 0.4 µM primer, 100 µM dNTPs, 2.5 mM Mg and 1 mM betaine.

Data Analysis

GWAS

Primary GWAS analysis was performed using the beta version of Efficient Mixed-Model Association eXpedited (EMMAX) [24]. We used a mixed model-based analysis to account for population stratification or cryptic relatedness that may have been present in the sample (as pedigrees were not available for cases). In addition, allelic associations with one million permutations were performed in PLINK (v1.07, [23]) to further assess association strength and rule out false positives. Permutation analysis consists of reassigning case-control labels randomly (in this case, through one million iterations) and then identifying the distribution of resultant associations at each SNP for all random case-control assignments. This normal distribution of possible associations is then compared to the actual phenotype association; the genome-wide permuted p-value represents the probability of seeing a spurious (random) association from the permutation-obtained normal distribution that is stronger than the observed association. For one million permutations, p = 1×10⁻⁶ states that no random association was stronger than the true finding. In the PLINK analysis, we did not correct for within-breed stratification by the incorporation of principal components or multi-dimensional scaling vectors, since the analyzed dogs had been genetically matched (Figure S1). Finally, haplotype analysis was performed in PLINK, with results visualized using the web-based Genome Variation Server (GVS) (http://gvs.gs.washington.edu/GVS/index.jsp) and Haploview.

NGS

Bowtie [25] was used for read alignment against CanFam2, allowing up to 2 mismatches in the first 60 bases of a given read. SAMtools [26], Picard (http://picard.sourceforge.net/), BEDTools [27], and the Genome Analysis Toolkit (GATK, [28]) were used for post-alignment processing. Multi-sample realignment around potential insertion/deletions (indels) and base quality score recalibration were both performed prior to variant calling by GATK's Unified Genotyper. Indels were called using Dindel [29]. ANNOVAR [30] was used to annotate and prioritize variants. Phastcons4way scores, which provide a measure of conservation based on multi-species alignment, were obtained from the UCSC Genome Browser [31].

Dye-terminator sequencing

Genotype calls for the three variants were made manually by inspection of sequence traces. Association testing was performed in PLINK, and false positives were assessed by subsequent permutation testing. Allele frequencies of variants between the Border Collies from the U.S. and Finland were not significantly different, according to Fisher's exact test for homogeneity; further, all associations remained when ancestry was added as a covariate (data not shown). The two groups were thus treated as a single group in follow-up analysis.

Meta-analysis of candidate variants

A sample size weighted analysis based on p-values generated in the primary and replication cohorts was performed using METAL [32].

Supporting Information

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