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德国短毛指示猎犬的家族性皮肤红斑狼疮(CLE)映射到 CFA18,这是犬类与人 CLE 的同源物。

Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE.

机构信息

School of Veterinary Medicine, Section of Medical Genetics, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Immunogenetics. 2011 Apr;63(4):197-207. doi: 10.1007/s00251-010-0499-z. Epub 2010 Dec 4.

Abstract

A familial form of lupus, termed exfoliative cutaneous lupus erythematosus (ECLE) has been recognized for decades in German shorthaired pointer dogs (GSP). Previous studies were suggestive of autosomal recessive inheritance. The disease presents as a severe dermatitis with age of onset between 16 and 40 weeks, and mirrors cutaneous lupus erythematosus (CLE) in humans. Lameness and, in advanced cases, renal disease may be present. Most affected dogs are euthanized before reaching the age of 4 years. The diagnosis is made by clinical observations and microscopic examination of skin biopsies. In humans, many different forms of CLE exist and various genes and chromosomal locations have been implicated. The large number of potential candidate loci combined with often weak association prevented in depth screening of the dog population thus far. During the course of our studies, we developed a colony of dogs with ECLE as a model for human CLE and the genetic analysis of these dogs confirmed the autosomal recessive mode of inheritance of CLE in GSPs. Using canine patient material, we performed a genome-wide association study (GWAS) to identify the genomic region harboring the gene involved in the development of the disease in GSPs. We identified a SNP allele on canine chromosome 18 that segregated with the disease in the 267 dogs tested. The data generated should allow identification of the mutant gene responsible for this form of cutaneous lupus erythematosus in dogs and assist in the understanding of the development of similar disease in humans.

摘要

一种家族性狼疮,称为剥脱性皮肤红斑狼疮 (ECLE),在德国短毛指示猎犬 (GSP) 中已被认识数十年。先前的研究表明该病为常染色体隐性遗传。这种疾病表现为严重的皮炎,发病年龄在 16 至 40 周之间,与人类的皮肤红斑狼疮 (CLE) 相似。可能出现跛行,在晚期病例中还可能出现肾脏疾病。大多数受影响的犬在 4 岁之前被安乐死。诊断是通过临床观察和皮肤活检的显微镜检查来做出的。在人类中,存在许多不同形式的 CLE,并且涉及到许多不同的基因和染色体位置。大量潜在的候选基因与通常较弱的关联,使得迄今为止对犬群的深入筛选变得复杂。在我们的研究过程中,我们开发了一个 ECLE 犬群作为人类 CLE 的模型,这些犬的遗传分析证实了 GSP 中 CLE 的常染色体隐性遗传模式。使用犬患者材料,我们进行了全基因组关联研究 (GWAS),以确定与 GSP 中疾病发展相关的基因所在的基因组区域。我们在 267 只测试犬中发现了位于犬 18 号染色体上的与疾病共分离的 SNP 等位基因。生成的数据应允许鉴定导致犬类这种形式皮肤红斑狼疮的突变基因,并有助于理解人类中类似疾病的发展。

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本文引用的文献

1
Lupoid Dermatosis in Five German Short-haired Pointers.五只德国短毛指示犬的类狼疮性皮肤病
Vet Dermatol. 1995 Jun;6(2):93-98. doi: 10.1111/j.1365-3164.1995.tb00049.x.
7
Review of recent genome-wide association scans in lupus.狼疮近期全基因组关联扫描综述。
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10
Clinical manifestations of cutaneous lupus erythematosus.皮肤红斑狼疮的临床表现。
J Dtsch Dermatol Ges. 2007 Dec;5(12):1124-37. doi: 10.1111/j.1610-0387.2007.06554.x.

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