Rando Halie M, Stutchman Jeremy T, Bastounes Estelle R, Johnson Jennifer L, Driscoll Carlos A, Barr Christina S, Trut Lyudmila N, Sacks Benjamin N, Kukekova Anna V
Department of Animal Science, College of Agricultural, Consumer and Environmental Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801; Laboratory of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892-9412; Institute of Cytology and Genetics of the Russian Academy of Sciences, Novosibirsk 630090, Russia; Mammalian Ecology and Conservation Unit, Veterinary Genetics Laboratory, School of Veterinary Medicine, University of California, Davis, CA 95616; Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.
J Hered. 2017 Sep 1;108(6):678-685. doi: 10.1093/jhered/esx066.
The de novo assembly of the red fox (Vulpes vulpes) genome has facilitated the development of genomic tools for the species. Efforts to identify the population history of red foxes in North America have previously been limited by a lack of information about the red fox Y-chromosome sequence. However, a megabase of red fox Y-chromosome sequence was recently identified over 2 scaffolds in the reference genome. Here, these scaffolds were scanned for repeated motifs, revealing 194 likely microsatellites. Twenty-three of these loci were selected for primer development and, after testing, produced a panel of 11 novel markers that were analyzed alongside 2 markers previously developed for the red fox from dog Y-chromosome sequence. The markers were genotyped in 76 male red foxes from 4 populations: 7 foxes from Newfoundland (eastern Canada), 12 from Maryland (eastern United States), and 9 from the island of Great Britain, as well as 48 foxes of known North American origin maintained on an experimental farm in Novosibirsk, Russia. The full marker panel revealed 22 haplotypes among these red foxes, whereas the 2 previously known markers alone would have identified only 10 haplotypes. The haplotypes from the 4 populations clustered primarily by continent, but unidirectional gene flow from Great Britain and farm populations may influence haplotype diversity in the Maryland population. The development of new markers has increased the resolution at which red fox Y-chromosome diversity can be analyzed and provides insight into the contribution of males to red fox population diversity and patterns of phylogeography.
赤狐(Vulpes vulpes)基因组的从头组装促进了该物种基因组工具的开发。此前,由于缺乏关于赤狐Y染色体序列的信息,确定北美赤狐种群历史的工作受到了限制。然而,最近在参考基因组的2个支架上鉴定出了100万个碱基对的赤狐Y染色体序列。在这里,对这些支架进行了重复基序扫描,发现了194个可能的微卫星。从这些位点中选择了23个用于引物开发,经过测试,产生了一组11个新的标记,并与之前从犬Y染色体序列开发的2个赤狐标记一起进行分析。对来自4个种群的76只雄性赤狐进行了基因分型:7只来自纽芬兰(加拿大东部),12只来自马里兰州(美国东部),9只来自大不列颠岛,以及48只已知原产于北美的赤狐,它们饲养在俄罗斯新西伯利亚的一个实验农场。完整的标记组在这些赤狐中揭示了22种单倍型,而仅2个先前已知的标记只能识别出10种单倍型。4个种群的单倍型主要按大陆聚类,但来自大不列颠岛和农场种群的单向基因流动可能会影响马里兰州种群的单倍型多样性。新标记的开发提高了分析赤狐Y染色体多样性的分辨率,并为雄性对赤狐种群多样性的贡献以及系统地理学模式提供了见解。