Abstract

Progressive retinal degenerations are among the most common causes of blindness both in human and in dogs. Canine progressive retinal atrophy (PRA) resembles human retinitis pigmentosa (RP) and is typically characterized by a progressive loss of rod photoreceptors followed by a loss of cone function. The disease gradually progress from the loss of night and day vision to a complete blindness. We have recently described a unique form of retinopathy characterized by the multifocal gray/brown discoloration and thinning of the retina in the Swedish Vallhund (SV) breed. We aimed to identify the genetic cause by performing a genome wide association analysis in a cohort of 18 affected and 10 healthy control dogs using Illumina's canine 22k SNP array. We mapped the disease to canine chromosome 17 (p = 7.7×10−5) and found a 6.1 Mb shared homozygous region in the affected dogs. A combined analysis of the GWAS and replication data with additional 60 dogs confirmed the association (p = 4.3×10−8, OR = 11.2 for homozygosity). A targeted resequencing of the entire associated region in four cases and four controls with opposite risk haplotypes identified several variants in the coding region of functional candidate genes, such as a known retinopathy gene, MERTK. However, none of the identified coding variants followed a compelling case- or breed-specific segregation pattern. The expression analyses of four candidate genes in the region, MERTK, NPHP1, ANAPC1 and KRCC1, revealed specific upregulation of MERTK in the retina of the affected dogs. Collectively, these results indicate that the retinopathy is associated with overexpression of MERTK, however further investigation is needed to discover the regulatory mutation for the better understanding of the disease pathogenesis. Our study establishes a novel gain-of-function model for the MERTK biology and provides a therapy model for retinopathy MERTK inhibitors. Meanwhile, a marker-based genetic counseling can be developed to revise breeding programs.

Highlights

  • Dogs suffer from hundreds of hereditary disorders according to the Online Mendelian Inheritance in Animal database (OMIA, http://omia.angis.org.au/ home/) and many of them represent clinically and physiologically relevant models for human conditions

  • We have previously identified a unique form of progressive retinal atrophies (PRA) in the Swedish Vallhund (SV) breed and show here genetic and functional evidence that the disease is associated with a known human Retinitis pigmentosa (RP) gene, mer protooncogene tyrosine kinase (MERTK)

  • The region harbors over 100 genes, including some that have been associated with retinal function or retinal degeneration in human and rodent models, such as anaphase promoting complex subunit 1 (ANAPC1), MERTK and nephronophthisis 1 (NPHP1)

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Summary

Introduction

Dogs suffer from hundreds of hereditary disorders according to the Online Mendelian Inheritance in Animal database (OMIA, http://omia.angis.org.au/ home/) and many of them represent clinically and physiologically relevant models for human conditions. Progressive retinal degenerations form a heterogeneous group of disorders that affect different retinal cells such as photoreceptors or retinal pigment epithelium (RPE), resulting in the impairment or complete loss of vision (RetNet; http://www.sph.uth.tmc.edu/Retnet/). PRA affects many breeds with remarkable variation in the etiology, progression and onset. Careful characterization of these conditions across breeds is important for the health of the dogs but could provide valuable information about the genetics, retinal biology, molecular pathogenesis of RPs and possible environmental factors complementing existing human studies. Over dozen PRA genes have been described in dogs [1], [3], [8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23], and many remain still to be found

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