A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs.

IF 2.9 Q2 Biochemistry, Genetics and Molecular Biology
Rebekkah J Hitti-Malin, Louise M Burmeister, Sally L Ricketts, Thomas W Lewis, Louise Pettitt, Mike Boursnell, Ellen C Schofield, David Sargan, Cathryn S Mellersh
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引用次数: 5

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.

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位于IMPG2启动子中的LINE-1插入与拉萨Apso犬的常染色体隐性进行性视网膜萎缩有关。
背景:犬进行性视网膜萎缩是犬的一组遗传性视网膜变性,其特征是视网膜中感光细胞的消耗,最终导致失明。拉萨Apso (LA)犬的PRA以前没有临床特征或在文献中描述过,但建议英国的主人每年通过英国兽医协会/养犬俱乐部/国际牧羊犬协会(BVA/KC/ISDS)眼科计划对他们的狗进行检查,其他国家也有类似的计划。在排除了25个先前报道的LA PRA影响犬的视网膜突变后,我们试图确定该品种PRA的遗传原因。结果:对3例受PRA影响的LA和3例无PRA症状的LA的全外显子组测序数据进行分析,未发现任何外显子或剪接位点变异,提示因果变异是非外显子的。随后,我们进行了一项全基因组关联研究(GWAS),在犬33号染色体上发现了一个1.3 Mb的疾病相关区域,随后进行了全基因组测序分析,发现在IMPG2基因上游有一个长穿插元件-1 (LINE-1)插入。IMPG2先前与人类视网膜疾病有关;然而,到目前为止,还没有犬类的PRAs与该基因有关。这种PRA相关变异的鉴定使得该品种中这种形式的PRA的DNA测试得以发展,这里称为PRA4,以区分它与其他品种中描述的其他形式的PRA。该测试已用于确定900多只洛杉矶犬的基因型。一大批基因型狗被用来估计等位基因频率在0.07-0.1之间。结论:通过使用GWAS和随后的PRA病例测序,我们已经确定了视网膜候选基因IMPG2中的LINE-1插入,该基因与LA犬的一种形式的PRA相关。在123个品种的447只狗身上验证了这种变异,确定它是洛杉矶狗的私人变异。我们设想,随着时间的推移,开发的DNA测试将为育种者提供机会,避免生产受这种形式的PRA影响的狗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genetics
BMC Genetics 生物-遗传学
CiteScore
4.30
自引率
0.00%
发文量
77
审稿时长
4-8 weeks
期刊介绍: BMC Genetics is an open access, peer-reviewed journal that considers articles on all aspects of inheritance and variation in individuals and among populations.
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