Melka Melkaye G, Schenkel Flavio S
Centre for Genetic Improvement of Livestock, Department of Animal and Poultry Science, University of Guelph, 50 Stone Road East, Ontario, N1G 2W1, Canada.
BMC Res Notes. 2012 Mar 22;5:161. doi: 10.1186/1756-0500-5-161.
Studies of genetic diversity are essential in understanding the extent of differentiation between breeds, and in designing successful diversity conservation strategies. The objective of this study was to evaluate the level of genetic diversity within and between North American Brown Swiss (BS, n = 900), Jersey (JE, n = 2,922) and Holstein (HO, n = 3,535) cattle, using genotyped bulls. GENEPOP and FSTAT software were used to evaluate the level of genetic diversity within each breed and between each pair of the three breeds based on genome-wide SNP markers (n = 50,972).
Hardy-Weinberg equilibrium (HWE) exact test within breeds showed a significant deviation from equilibrium within each population (P < 0.01), which could be a result of selection, genetic drift and inbreeding within each breed. Hardy-Weinberg test also confirmed significant heterozygote deficit in each breed over several loci. Moreover, results from population differentiation tests showed that the majority of loci have alleles or genotypes drawn from different distributions in each breed. Average gene diversity, expressed in terms of observed heterozygosity, over all loci in BS, JE and HO was 0.27, 0.26 and 0.31, respectively. The proportion of genetic diversity due to allele frequency differences among breeds (Fst) indicated that the combination of BS and HO in an ideally amalgamated population had higher genetic diversity than the other pairs of breeds.
Results suggest that the three bull populations have substantially different gene pools. BS and HO show the largest gene differentiation and jointly the highest total expected gene diversity compared to when JE is considered. If the loss of genetic diversity within breeds worsens in the future, the use of crossbreeding might be an option to recover genetic diversity, especially for the breeds with small population size.
遗传多样性研究对于理解品种间的分化程度以及设计成功的多样性保护策略至关重要。本研究的目的是利用基因分型公牛评估北美褐牛(BS,n = 900)、泽西牛(JE,n = 2922)和荷斯坦牛(HO,n = 3535)群体内部和群体之间的遗传多样性水平。使用GENEPOP和FSTAT软件,基于全基因组SNP标记(n = 50972)评估每个品种内部以及三个品种两两之间的遗传多样性水平。
品种内的哈迪-温伯格平衡(HWE)精确检验显示,每个群体内均存在显著偏离平衡的情况(P < 0.01),这可能是每个品种内选择、遗传漂变和近亲繁殖的结果。哈迪-温伯格检验还证实,每个品种在多个位点上均存在显著的杂合子缺失。此外,群体分化测试结果表明,大多数位点的等位基因或基因型在每个品种中的分布不同。以观察到的杂合度表示的平均基因多样性,在BS、JE和HO的所有位点上分别为0.27、0.26和0.31。品种间等位基因频率差异导致的遗传多样性比例(Fst)表明,在理想合并群体中,BS和HO的组合比其他品种对具有更高的遗传多样性。
结果表明,这三个公牛群体具有显著不同的基因库。与考虑JE时相比,BS和HO表现出最大的基因分化,并且共同具有最高的总预期基因多样性。如果未来品种内遗传多样性的丧失加剧,杂交可能是恢复遗传多样性的一种选择,特别是对于小群体品种。