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在大量受欢迎的猫品种中发现了广泛的视网膜退行性疾病突变(rdAc)。

Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds.

机构信息

Laboratory of Genomic Diversity, National Cancer Institute-Frederick, Frederick, MD 21702, USA.

出版信息

Vet J. 2010 Oct;186(1):32-8. doi: 10.1016/j.tvjl.2009.08.010. Epub 2009 Sep 10.

Abstract

The recent discovery of a mutational variant in the CEP290 gene (CEP290: IVS50+9T>G), conferring recessive retinal degeneration in Abyssinian and Somali (long-haired Abyssinian) cats (rdAc) prompted a survey among 41 cat breeds (846 individuals) to assess the incidence, frequency and clinical consequence of rdAc. The rdAc allele displayed widespread distribution, observed in 16/43 (37%) breeds, exhibiting a high allele frequency (∼33%) in North American and European Siamese populations. Clinical evaluations demonstrated high concordance between rdAc pathology and the CEP290 (IVS50+9T>G) homozygous genotype (P=1.1E-6), with clinical disease similar to affected Abyssinians/Somalis. This retinal degeneration has not been reported in breeds other than the Abyssinian/Somali and poses a significant health risk particularly in the Siamese breed group. Alertness of the veterinary community and the present availability of commercial diagnostic testing could synergistically enable breeders to reduce the incidence of rdAc blindness in pure-bred cat populations.

摘要

最近在 CEP290 基因(CEP290:IVS50+9T>G)中发现了一个突变变体,导致阿比西尼亚猫和索马里猫(长毛阿比西尼亚猫)(rdAc)出现隐性视网膜变性,这促使对 41 个猫品种(846 只个体)进行了调查,以评估 rdAc 的发病率、频率和临床后果。rdAc 等位基因分布广泛,在 37%的 16/43 个品种中观察到,在北美和欧洲的暹罗种群中具有较高的等位基因频率(约 33%)。临床评估表明 rdAc 病理学与 CEP290(IVS50+9T>G)纯合基因型之间具有高度一致性(P=1.1E-6),临床疾病与受影响的阿比西尼亚猫/索马里猫相似。这种视网膜变性除了阿比西尼亚猫/索马里猫之外,在其他品种中尚未有报道,并且在暹罗品种群体中存在重大健康风险。兽医界的警觉性和商业诊断测试的现有可用性可以协同作用,使饲养者能够降低纯种猫群体中 rdAc 失明的发病率。

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