在英国,为消除微型线毛腊肠的拉福拉病而进行的全国性基因检测。

Canine genetics and epidemiology Pub Date : 2018-03-27 eCollection Date: 2018-01-01 DOI:10.1186/s40575-018-0058-8
Saija Ahonen, Ian Seath, Clare Rusbridge, Susan Holt, Gill Key, Travis Wang, Peixiang Wang, Berge A Minassian
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引用次数: 13

摘要

犬dna检测已成为纯种犬育种的重要工具,许多育种者在制定育种策略时使用基因检测结果。此外,从一个品种的数百只狗的测试中获得的信息提供了有关疾病相关等位基因的全品种基因型频率的宝贵信息。拉福拉病是一种发病晚、隐性遗传的遗传病,主要发生在微型带毛腊肠犬(MWHD)身上。这是犬类癫痫最严重的形式之一,会导致神经退化,通常在诊断后几年内就会安乐死。犬拉福拉病是由NHLRC1基因的十二聚体重复扩增突变引起的,DNA测试可用于识别有风险的纯合子狗、携带者和没有突变的狗。结果:从全球733名mwhd(主要来自英国)收集血液样本,用于犬拉福拉病检测。在检测的MWHD群体中,7.0%的人突变为纯合子,有拉福拉病的危险。此外,234只狗是杂合子,表明在受测人群中携带频率为31.9%。在所检测的MWHDs中,突变等位基因频率为0.2。此外,6年(2012-2017)的测试数据表明,在测试的mwhd中,纯合子和携带犬的频率分别从10.4%下降到2.7%和41.5%下降到25.7%。结果,没有突变的狗的频率从48.1%增加到71.6%。结论:本研究为MWHD社区提供了有价值的数据,表明DNA检测是育种者预防MWHD拉福拉病发生的有效工具。在过去的六年里,DNA检测有助于降低携带者和处于危险中的狗的频率。此外,DNA测试可以继续用于慢慢根除该品种的致病突变。然而,这应该谨慎地进行,随着时间的推移,以避免进一步损害品种的遗传多样性。如果兽医看到狗狗出现与拉福拉病相关的临床症状,DNA测试也为兽医提供了一种诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom.

Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom.

Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom.

Background: Canine DNA-testing has become an important tool in purebred dog breeding and many breeders use genetic testing results when planning their breeding strategies. In addition, information obtained from testing of hundreds dogs in one breed gives valuable information about the breed-wide genotype frequency of disease associated allele. Lafora disease is a late onset, recessively inherited genetic disease which is diagnosed in Miniature Wirehaired Dachshunds (MWHD). It is one of the most severe forms of canine epilepsy leading to neurodegeneration and, frequently euthanasia within a few years of diagnosis. Canine Lafora disease is caused by a dodecamer repeat expansion mutation in the NHLRC1 gene and a DNA test is available to identify homozygous dogs at risk, carriers and dogs free of the mutation.

Results: Blood samples were collected from 733 MWHDs worldwide, mostly of UK origin, for canine Lafora disease testing. Among the tested MWHD population 7.0% were homozygous for the mutation and at risk for Lafora disease. In addition, 234 dogs were heterozygous, indicating a carrier frequency of 31.9% in the tested population. Among the tested MWHDs, the mutant allele frequency was 0.2. In addition, data from the tested dogs over 6 years (2012-2017) indicated that the frequency of the homozygous and carrier dogs has decreased from 10.4% to 2.7% and 41.5% to 25.7%, respectively among MWHDs tested. As a consequence, the frequency of dogs free of the mutation has increased from 48.1% to 71.6%.

Conclusions: This study provides valuable data for the MWHD community and shows that the DNA test is a useful tool for the breeders to prevent occurrence of Lafora disease in MWHDs. DNA testing has, over 6 years, helped to decrease the frequency of carriers and dogs at risk. Additionally, the DNA test can continue to be used to slowly eradicate the disease-causing mutation in the breed. However, this should be done carefully, over time, to avoid further compromising the genetic diversity of the breed. The DNA test also provides a diagnostic tool for veterinarians if they are presented with a dog that shows clinical signs associated with canine Lafora disease.

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