Oliver James A C, Forman Oliver P, Pettitt Louise, Mellersh Cathryn S
Department of Canine Genetics Research, Centre for Preventive Medicine, Animal Health Trust, Newmarket, Suffolk, United Kingdom.
PLoS One. 2015 Oct 16;10(10):e0140436. doi: 10.1371/journal.pone.0140436. eCollection 2015.
Mutations in ADAMTS10 (CFA20) have previously been associated with primary open angle glaucoma (POAG) in the Beagle and Norwegian Elkhound. The closely related gene, ADAMTS17, has also been associated with several different ocular phenotypes in multiple breeds of dog, including primary lens luxation and POAG. We investigated ADAMTS17 as a candidate gene for POAG in the Basset Hound and Basset Fauve de Bretagne dog breeds.
We performed ADAMTS17 exon resequencing in three Basset Hounds and three Basset Fauve de Bretagne dogs with POAG. Identified variants were genotyped in additional sample cohorts of both breeds and dogs of other breeds to confirm their association with disease.
All affected Basset Hounds were homozygous for a 19 bp deletion in exon 2 that alters the reading frame and is predicted to lead to a truncated protein. Fifty clinically unaffected Basset Hounds were genotyped for this mutation and all were either heterozygous or homozygous for the wild type allele. Genotyping of 223 Basset Hounds recruited for a different study revealed a mutation frequency of 0.081 and predicted frequency of affected dogs in the population to be 0.007. Based on the entire genotyping dataset the association statistic for the POAG-associated deletion was p = 1.26 x 10-10. All affected Basset Fauve de Bretagne dogs were homozygous for a missense mutation in exon 11 causing a glycine to serine amino acid substitution (G519S) in the disintegrin-like domain of ADAMTS17 which is predicted to alter protein function. Unaffected Basset Fauve de Bretagne dogs were either heterozygous for the mutation (5/24) or homozygous for the wild type allele (19/24). Based on the entire genotyping dataset the association statistic for the POAG-associated deletion was p = 2.80 x 10-7. Genotyping of 85 dogs of unrelated breeds and 90 dogs of related breeds for this variant was negative.
This report documents strong associations between two independent ADAMTS17 mutations and POAG in two different dog breeds.
ADAMTS10(犬20号染色体)突变先前已被证实与比格犬和挪威猎麋犬的原发性开角型青光眼(POAG)有关。与之密切相关的基因ADAMTS17也与多个犬种的几种不同眼部表型有关,包括原发性晶状体脱位和POAG。我们研究了ADAMTS17作为巴吉度猎犬和布列塔尼浅黄褐色矮腿猎犬POAG候选基因的可能性。
我们对3只患有POAG的巴吉度猎犬和3只布列塔尼浅黄褐色矮腿猎犬进行了ADAMTS17外显子重测序。在这两个品种以及其他品种犬的额外样本队列中对鉴定出的变异进行基因分型,以确认它们与疾病的关联。
所有患病巴吉度猎犬在第2外显子中有一个19bp的缺失,该缺失改变了阅读框,预计会导致蛋白质截短,所有患病犬均为该缺失的纯合子。对50只临床未患病的巴吉度猎犬进行该突变的基因分型,所有犬要么是野生型等位基因的杂合子,要么是纯合子。对为另一项研究招募的223只巴吉度猎犬进行基因分型,发现突变频率为0.081,预计该群体中患病犬的频率为0.007。基于整个基因分型数据集,与POAG相关的缺失的关联统计量为p = 1.26×10 - 10。所有患病的布列塔尼浅黄褐色矮腿猎犬在第11外显子中有一个错义突变,导致ADAMTS17的解整合素样结构域中的甘氨酸被丝氨酸取代(G519S),预计这会改变蛋白质功能,所有患病犬均为该突变的纯合子。未患病的布列塔尼浅黄褐色矮腿猎犬要么是该突变的杂合子(5/24),要么是野生型等位基因的纯合子(19/24)。基于整个基因分型数据集,与POAG相关的缺失的关联统计量为p = 2.80×10 - 7。对85只无关品种犬和90只相关品种犬进行该变异的基因分型,结果均为阴性。
本报告记录了两个独立的ADAMTS17突变与两个不同犬种的POAG之间的强关联。