Niskanen Julia, Dillard Kati, Arumilli Meharji, Salmela Elina, Anttila Marjukka, Lohi Hannes, Hytönen Marjo K
Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
PLoS One. 2017 May 11;12(5):e0177527. doi: 10.1371/journal.pone.0177527. eCollection 2017.
A rare hereditary mechanobullous disorder called epidermolysis bullosa (EB) causes blistering in the skin and the mucosal membranes. To date, nineteen EB-related genes have been discovered in human and other species. We describe here a novel EB variant in dogs. Two newborn littermates of Central Asian Shepherd dogs with severe signs of skin blistering were brought to a veterinary clinic and euthanized due to poor prognosis. In post-mortem examination, the puppies were shown to have findings in the skin and the mucosal membranes characteristic of EB. A whole-genome sequencing of one of the affected puppies was performed to identify the genetic cause. The resequencing data were filtered under a recessive model against variants from 31 other dog genomes, revealing a homozygous case-specific nonsense variant in one of the known EB-causing genes, COL7A1 (c.4579C>T, p.R1527*). The variant results in a premature stop codon and likely absence of the functional protein in the basement membrane of the skin in the affected dogs. This was confirmed by immunohistochemistry using a COL7A1 antibody. Additional screening of the variant indicated full penetrance and breed specificity at ~28% carrier frequency. In summary, this study reveals a novel COL7A1 variant causing recessive dystrophic EB and provides a genetic test for the eradication of the disease from the breed.
一种罕见的遗传性机械性大疱性疾病,称为大疱性表皮松解症(EB),会导致皮肤和黏膜出现水疱。迄今为止,已在人类和其他物种中发现了19个与EB相关的基因。我们在此描述犬类中的一种新型EB变体。两只患有严重皮肤水疱症状的中亚牧羊犬新生同窝幼犬被带到兽医诊所,由于预后不良而实施安乐死。在尸检中,这些幼犬被发现具有EB特有的皮肤和黏膜病变。对其中一只患病幼犬进行了全基因组测序,以确定遗传病因。根据隐性模型对重测序数据进行筛选,与来自其他31个犬类基因组的变体进行比对,结果显示在已知的一个导致EB的基因COL7A1中存在一个纯合的病例特异性无义变体(c.4579C>T,p.R1527*)。该变体导致过早出现终止密码子,受影响犬类皮肤基底膜中可能缺乏功能性蛋白。使用COL7A1抗体进行免疫组织化学证实了这一点。对该变体的进一步筛查表明其具有完全外显率和约28%的携带频率的品种特异性。总之,本研究揭示了一种导致隐性营养不良性EB的新型COL7A1变体,并为从该品种中根除该疾病提供了基因检测方法。