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首页> 外文期刊>Canine Genetics and Epidemiology >Heterozygosity testing and multiplex DNA panel screening as a potential tool to monitor health and inbreeding in a small, closed dog population
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Heterozygosity testing and multiplex DNA panel screening as a potential tool to monitor health and inbreeding in a small, closed dog population

机译:杂合性测试和多重DNA面板筛选是监测封闭的小型犬群健康和近亲繁殖的潜在工具

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Background Selective breeding in populations with a limited effective population size may result in a loss of genetic diversity, which can cause an increased concentration of specific disease liability genes. The Dutch Shepherd Dog (DSD) in the Netherlands is an example of such a breed with a small effective population. Objective To evaluate the measurement of genetic diversity and multiplex DNA panel screening for implementation in a breeding strategy for the Dutch Shepherd Dog (DSD) and to investigate the clinical relevance of potentially identified mutations in the multiplex DNA panel screening. Results Genome-wide SNP testing showed genetic isolation and reduced genetic diversity within coat variety subgroups of the DSD. Panel screening identified a Von Willebrand’s Disease type I mutation. Although decreased Von Willebrand’s Factor proteins were significantly lower in DSDs carrying the VWD-I allele compared to the wildtype, clinical follow-up did not show a significant association between the clinical phenotype and VWD-I genotype. Conclusions Genetic relationship measurement within a breed population may be a useful tool to enable breeding strategies to conserve genetic diversity. Results from a disease panel screening need to be evaluated for clinical relevance before breed selection restrictions can be considered.
机译:背景技术在有效种群数量有限的人群中进行选择性育种可能会导致遗传多样性的丧失,从而可能导致特定疾病责任基因的浓度增加。荷兰的荷兰牧羊犬(DSD)就是这样一个有效种群很少的品种。目的评估遗传多样性和多重DNA面板筛选在荷兰牧羊犬(DSD)繁殖策略中的应用,并研究多重DNA面板筛选中潜在鉴定出的突变的临床相关性。结果全基因组SNP测试显示DSD的被毛品种亚组内遗传分离并减少了遗传多样性。小组筛查确定了Von Willebrand的I型疾病突变。尽管与野生型相比,携带VWD-1等位基因的DSD中Von Willebrand因子蛋白的降低显着降低,但临床随访并未显示临床表型与VWD-1基因型之间的显着关联。结论在一个种群中进行亲缘关系测量可能是使育种策略能够保护遗传多样性的有用工具。在考虑品种选择限制之前,需要评估疾病小组筛查的结果的临床相关性。

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