Abstract
Abstract
Background
Canine progressive retinal atrophies are a group of hereditary retinal degenerations in dogs characterised by depletion of photoreceptor cells in the retina, which ultimately leads to blindness. PRA in the Lhasa Apso (LA) dog has not previously been clinically characterised or described in the literature, but owners in the UK are advised to have their dog examined through the British Veterinary Association/ Kennel Club/ International Sheep Dog Society (BVA/KC/ISDS) eye scheme annually, and similar schemes that are in operation in other countries. After the exclusion of 25 previously reported canine retinal mutations in LA PRA-affected dogs, we sought to identify the genetic cause of PRA in this breed.
Results
Analysis of whole-exome sequencing data of three PRA-affected LA and three LA without signs of PRA did not identify any exonic or splice site variants, suggesting the causal variant was non-exonic. We subsequently undertook a genome-wide association study (GWAS), which identified a 1.3 Mb disease-associated region on canine chromosome 33, followed by whole-genome sequencing analysis that revealed a long interspersed element-1 (LINE-1) insertion upstream of the IMPG2 gene. IMPG2 has previously been implicated in human retinal disease; however, until now no canine PRAs have been associated with this gene. The identification of this PRA-associated variant has enabled the development of a DNA test for this form of PRA in the breed, here termed PRA4 to distinguish it from other forms of PRA described in other breeds. This test has been used to determine the genotypes of over 900 LA dogs. A large cohort of genotyped dogs was used to estimate the allele frequency as between 0.07–0.1 in the UK LA population.
Conclusions
Through the use of GWAS and subsequent sequencing of a PRA case, we have identified a LINE-1 insertion in the retinal candidate gene IMPG2 that is associated with a form of PRA in the LA dog. Validation of this variant in 447 dogs of 123 breeds determined it was private to LA dogs. We envisage that, over time, the developed DNA test will offer breeders the opportunity to avoid producing dogs affected with this form of PRA.
Funder
Petplan Charitable Trust
Lhasa Apso Breed Council
Kennel Club Charitable Trust UK
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference97 articles.
1. Méndez-Vidal C, Bravo-Gil N, González-Del Pozo M, Vela-Boza A, Dopazo J, Borrego S, Antiñolo G. Novel RP1 mutations and a recurrent BBS1variant explain the co-existence of two distinct retinal phenotypes in the same pedigree. BMC Genetics. 2014;15:143.
2. RetNet, the Retinal Information Network. http://www.sph.uth.tmc.edu/RetNet/. Accessed 8 Oct 2019.
3. Petersen-Jones SM, Komaromy AM. Dog models for blinding inherited retinal dystrophies. Human Gene Ther Clin Dev. 2015;26(1):15–26.
4. Parry HB. Degenerations of the dog retina. II. Generalized progressive atrophy of hereditary origin. Br J Ophthalmol. 1953;37(8):487–502.
5. Gelatt KN, Gilger BC, Kern TJ. In: Gelatt KN, Gilger BC, Kern TJ, editors. Veterinary ophthalmology, vol. 1. 5th ed. United States: Ames, Iowa: Wiley-Blackwell; 2013.
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献