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

机译:位于IMP1的启动子中的线1插入与Lhasa Apso狗的常染色体隐性渐进式视网膜萎缩相关联

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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. 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. 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.
机译:犬进化视网膜萎缩萎缩剂是一种遗传性视网膜退化,其特征在于视网膜中的感光细胞枯竭,这最终导致失明。 Lhasa Apso(La)狗的PRA先前没有在文献中被描述或描述,但建议英国的业主通过英国兽医协会/狗窝俱乐部/国际羊狗社会(BVA / KC / ISDS)眼睛方案每年,以及在其他国家的运作中的类似方案。排除25份以前报道的犬类视网膜突变,我们试图识别PRA在这种品种中的遗传原因。分析三个PRA受影响的LA和3La的全外膜测序数据,没有PRA的迹象没有识别任何偏僻的或接头位点变体,表明因果变形是非偏离的。我们随后进行了一种基因组 - 宽的协会研究(GWAs),其在犬染色体33上鉴定了1.3μm病相关区域,其次是全基因组测序分析,揭示了散射的元素-1(线-1)的上游插入IMP12基因。 IMPG2以前涉及人类视网膜疾病;然而,直到现在,没有犬PRA已经与该基因有关。该PRA相关变体的鉴定使得在品种中的这种形式的PRA进行DNA测试,这里称为PRA4以将其与其他品种中描述的其他形式的PRA区分开来。该测试已用于确定超过900只LA狗的基因型。使用大型基因分型犬用于估计英国LA群中的等位基因频率,如0.07-0.1。通过使用GWA和PRA案例的随后测序,我们已经确定了在视网膜候选基因IMPG2中的线1插入,其与LA狗中的PRA形式相关。在447名犬的447名狗的验证确定它是La狗的私人。我们设想,随着时间的推移,发达的DNA测试将提供育种者有机会避免生产受这种形式的PRA影响的狗。

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