首页> 外文期刊>The Open Genomics Journal >Primary Lens Luxation in Australian Tenterfield and Miniature Bull Terriers is Due to An Old ADAMTS17 Mutation and is an Additive Trait
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Primary Lens Luxation in Australian Tenterfield and Miniature Bull Terriers is Due to An Old ADAMTS17 Mutation and is an Additive Trait

机译:澳大利亚Tenterfield和小型斗牛梗的主要晶状体脱位归因于旧的ADAMTS17突变,是一种附加性状

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Primary Lens Luxation (PLL) is an inherited disease common in Terrier breeds. A truncating mutation in the ADAMTS17 orthologue on CFA03 is reported to cause PLL in 17 breeds, mostly Terriers. This study investigated the mode of inheritance and penetrance of PLL, age of the ADAMTS17mutation, and other possible causes of PLL inAustralian Tenterfield Terriers and Miniature Bull Terriers. The ADAMTS17mutation and 30 nearby microsatellites on CFA03 were genotyped in 66 Australian Tenterfield Terriers, and 74 Miniature Bull Terriers. Lifetime risk of developing clinical PLL in homozygote and heterozygous animals, penetrance of PLL in general population, and recurrence risk of the disease for offspring and siblings of an index case was estimated. The effect of the ADAMTS17mutation on the risk ofPLL was dose and age dependent, and best fitted an additive model. Primary lens luxation was fully penetrant in homozygotes over 6 years and incompletely penetrant with a significant risk of PLL in heterozygote animals. Microsatellite haplotype testing estimated the mutation to be an old mutation, consistent with its appearance on severaldifferent background haplotypes and suggesting it entered the tested Tenterfield Terrier population at least three times,and the tested Miniature Bull Terrier population once. Finite polygenic model and survival analyses suggested that the ADAMTS17mutation is the main cause of PLL in these breeds, and if the PLL phenotype is controlled by factors other than this mutation, such as a second locus or an environmental effect, the effect is much less than that of this disease associated SNP.
机译:原发性晶状体脱位(PLL)是梗犬品种中常见的遗传疾病。据报道,CFA03上ADAMTS17直向同源物的截短突变导致17个品种(主要是梗犬)中的PLL。本研究调查了澳大利亚Tenterfield梗犬和微型斗牛梗的PLL的继承和渗透模式,ADAMTS17突变的年龄以及PLL的其他可能原因。 CFA03上的ADAMTS17突变和附近的30个微卫星在66个澳大利亚Tenterfield梗犬和74个微型斗牛犬中进行了基因分型。评估了纯合子和杂合动物中发展临床PLL的终生风险,普通人群中PLL的穿透性以及该疾病对后代和同胞兄弟姐妹的复发风险。 ADAMTS17突变对PLL风险的影响与剂量和年龄有关,最适合于加性模型。原发性晶状体脱位在纯合子中超过6年完全渗透,在杂合子动物中不完全渗透且有PLL的显着风险。微卫星单倍型测试估计该突变为旧突变,与它在几种不同背景单倍型上的出现一致,表明它至少进入了测试的Tenterfield Terrier种群三倍,进入了测试的微型Bull Terrier种群一次。有限的多基因模型和生存分析表明,ADAMTS17突变是这些品种中PLL的主要原因,并且如果PLL表型受该突变以外的因素控制,例如第二基因座或环境效应,则其影响远小于这种疾病相关的SNP。

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