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      Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders

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          Abstract

          Background

          The growing number of identified genetic disease risk variants across dog breeds challenges the current state-of-the-art of population screening, veterinary molecular diagnostics, and genetic counseling. Multiplex screening of such variants is now technologically feasible, but its practical potential as a supportive tool for canine breeding, disease diagnostics, pet care, and genetics research is still unexplored.

          Results

          To demonstrate the utility of comprehensive genetic panel screening, we tested nearly 7000 dogs representing around 230 breeds for 93 disease-associated variants using a custom-designed genotyping microarray (the MyDogDNA® panel test). In addition to known breed disease-associated mutations, we discovered 15 risk variants in a total of 34 breeds in which their presence was previously undocumented. We followed up on seven of these genetic findings to demonstrate their clinical relevance. We report additional breeds harboring variants causing factor VII deficiency, hyperuricosuria, lens luxation, von Willebrand’s disease, multifocal retinopathy, multidrug resistance, and rod-cone dysplasia. Moreover, we provide plausible molecular explanations for chondrodysplasia in the Chinook, cerebellar ataxia in the Norrbottenspitz, and familiar nephropathy in the Welsh Springer Spaniel.

          Conclusions

          These practical examples illustrate how genetic panel screening represents a comprehensive, efficient and powerful diagnostic and research discovery tool with a range of applications in veterinary care, disease research, and breeding. We conclude that several known disease alleles are more widespread across different breeds than previously recognized. However, careful follow up studies of any unexpected discoveries are essential to establish genotype-phenotype correlations, as is readiness to provide genetic counseling on their implications for the dog and its breed.

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          Most cited references25

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          Ivermectin sensitivity in collies is associated with a deletion mutation of the mdr1 gene.

          A subpopulation of collie dogs is extremely sensitive to neurotoxicity induced by ivermectin. The aim of this study was to determine the mechanistic basis for this phenomenon. The multi-drug-resistance gene (mdr1) encodes a large transmembrane protein, P-glycoprotein (P-gp), that is an integral part of the blood-brain barrier. P-gp functions as a drug-transport pump at the blood-brain barrier, transporting a variety of drugs from the brain back into the blood. Since ivermectin is a substrate for P-gp, we hypothesized that ivermectin-sensitive collies had altered mdr1 expression compared with unaffected collies. We report a deletion mutation of the mdr1 gene that is associated with ivermectin sensitivity. The 4-bp deletion results in a frame shift, generating several stop codons that prematurely terminate P-gp synthesis. Dogs that are homozygous for the deletion mutation display the ivermectin-sensitive phenotype, while those that are homozygous normal or heterozygous do not display increased sensitivity to ivermectin.
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            Breed relationships facilitate fine-mapping studies: a 7.8-kb deletion cosegregates with Collie eye anomaly across multiple dog breeds.

            The features of modern dog breeds that increase the ease of mapping common diseases, such as reduced heterogeneity and extensive linkage disequilibrium, may also increase the difficulty associated with fine mapping and identifying causative mutations. One way to address this problem is by combining data from multiple breeds segregating the same trait after initial linkage has been determined. The multibreed approach increases the number of potentially informative recombination events and reduces the size of the critical haplotype by taking advantage of shortened linkage disequilibrium distances found across breeds. In order to identify breeds that likely share a trait inherited from the same ancestral source, we have used cluster analysis to divide 132 breeds of dog into five primary breed groups. We then use the multibreed approach to fine-map Collie eye anomaly (cea), a complex disorder of ocular development that was initially mapped to a 3.9-cM region on canine chromosome 37. Combined genotypes from affected individuals from four breeds of a single breed group significantly narrowed the candidate gene region to a 103-kb interval spanning only four genes. Sequence analysis revealed that all affected dogs share a homozygous deletion of 7.8 kb in the NHEJ1 gene. This intronic deletion spans a highly conserved binding domain to which several developmentally important proteins bind. This work both establishes that the primary cea mutation arose as a single disease allele in a common ancestor of herding breeds as well as highlights the value of comparative population analysis for refining regions of linkage.
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              Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies.

              Considerable clinical and molecular variations have been known in retinal blinding diseases in man and also in dogs. Different forms of retinal diseases occur in specific breed(s) caused by mutations segregating within each isolated breeding population. While molecular studies to find genes and mutations underlying retinal diseases in dogs have benefited largely from the phenotypic and genetic uniformity within a breed, within- and across-breed variations have often played a key role in elucidating the molecular basis. The increasing knowledge of phenotypic, allelic, and genetic heterogeneities in canine retinal degeneration has shown that the overall picture is rather more complicated than initially thought. Over the past 20 years, various approaches have been developed and tested to search for genes and mutations underlying genetic traits in dogs, depending on the availability of genetic tools and sample resources. Candidate gene, linkage analysis, and genome-wide association studies have so far identified 24 mutations in 18 genes underlying retinal diseases in at least 58 dog breeds. Many of these genes have been associated with retinal diseases in humans, thus providing opportunities to study the role in pathogenesis and in normal vision. Application in therapeutic interventions such as gene therapy has proven successful initially in a naturally occurring dog model followed by trials in human patients. Other genes whose human homologs have not been associated with retinal diseases are potential candidates to explain equivalent human diseases and contribute to the understanding of their function in vision.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                15 August 2016
                2016
                : 11
                : 8
                : e0161005
                Affiliations
                [1 ]Genoscoper Laboratories Oy, Helsinki, Finland
                [2 ]Research Programs Unit—Molecular Neurology, University of Helsinki, Helsinki, Finland
                [3 ]Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland
                [4 ]Folkhälsan Institute of Genetics, Helsinki, Finland
                [5 ]Department of Equine and Small Animal Medicine, University of Helsinki, Helsinki, Finland
                [6 ]Section of Medical Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
                University of Sydney Faculty of Veterinary Science, AUSTRALIA
                Author notes

                Competing Interests: HL is a co-founder of Genoscoper Laboratories Oy that offers canine DNA testing as a commercial service. JD, HA, and FM are employees of Genoscoper Laboratories. UG heads the PennGen laboratory at the University of Pennsylvania. MH, MK, KK, and SS declare that no competing interests exist. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.

                • Conceived and designed the experiments: JD HL UG.

                • Performed the experiments: JD MK HA FM KK SS MH.

                • Analyzed the data: JD.

                • Wrote the paper: JD MK HA KK SS MH UG HL.

                Article
                PONE-D-16-18802
                10.1371/journal.pone.0161005
                4985128
                27525650
                972a820f-1e26-4c82-80c6-c9282f2137a0
                © 2016 Donner et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 10 May 2016
                : 28 July 2016
                Page count
                Figures: 4, Tables: 2, Pages: 18
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100004012, Jane ja Aatos Erkon Säätiö;
                Award Recipient :
                Funded by: Biocentrum Helsinki
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100003125, Suomen Kulttuurirahasto;
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100002341, Suomen Akatemia;
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: OD010939
                Award Recipient :
                This study was partly supported by the Jane and Aatos Erkko Foundation ( http://www.jaes.fi/; to HL), Biocentrum Helsinki ( http://www.helsinki.fi/biocentrum/; to HL), the Finnish Cultural Foundation ( http://www.skr.fi; to KK), the Academy of Finland ( http://www.aka.fi/fi/; to HL), and National Institutes of Health grant number OD010939 – Animal Models of Human Genetic Disease ( http://www.nih.gov; to UG). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Organisms
                Animals
                Animal Types
                Pets and Companion Animals
                Biology and Life Sciences
                Zoology
                Animal Types
                Pets and Companion Animals
                Biology and Life Sciences
                Organisms
                Animals
                Vertebrates
                Amniotes
                Mammals
                Dogs
                Biology and Life Sciences
                Genetics
                Gene Identification and Analysis
                Genetic Screens
                Biology and Life Sciences
                Genetics
                Genetics of Disease
                Biology and Life Sciences
                Veterinary Science
                Veterinary Medicine
                Veterinary Diagnostics
                Biology and Life Sciences
                Veterinary Science
                Veterinary Diseases
                Biology and Life Sciences
                Behavior
                Animal Behavior
                Animal Sexual Behavior
                Biology and Life Sciences
                Zoology
                Animal Behavior
                Animal Sexual Behavior
                Medicine and Health Sciences
                Clinical Genetics
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