Winters M, Torkelson A, Booth R, Mailand C, Hoareau Y, Tucker S, Wasser S K
Center for Conservation Biology, Department of Biology, University of Washington, Seattle, WA, USA.
Center for Conservation Biology, Department of Biology, University of Washington, Seattle, WA, USA.
Forensic Sci Int. 2018 Jul;288:131-139. doi: 10.1016/j.forsciint.2018.04.036. Epub 2018 Apr 27.
Genotyping ivory samples can determine the geographic origin of poached ivory as well as the legality of ivory being sold in ivory markets. We conducted a series of experiments to determine where the DNA is most concentrated in ivory samples and how best to increase DNA yield from groups of samples likely to vary in DNA concentration. We examined variation in DNA amplification success from: the layer(s) of the tusk (cementum and/or dentine) being extracted, demineralization temperature and time, and the concentration of eluates. Since demineralization of the pulverized sample produces a pellet and supernatant, we also assessed DNA amplification success from the pellet, the supernatant, their combination, as well as variation in the respective amounts used for extraction. Our results show that the outer cementum layer of the tusk contains the highest concentration of DNA and should be separated and used exclusively as the source material of ivory processed for extraction, when available. Utilizing the combined demineralized lysate improves extraction efficiency, as does increasing demineralization time to 3 or more days, conducted at 4°C. The most significant improvements occurred for low template DNA ivory samples followed by medium quality samples. Amplification success of high quality samples was not affected by these changes. Application of this optimized method to 3068 ivory samples resulted in 81.2% of samples being confirmed for both alleles at a minimum of 10 out of 16 microsatellite loci, which is our threshold for inclusion in DNA assignment analyses.
对象牙样本进行基因分型可以确定偷猎象牙的地理来源以及象牙市场上所售象牙的合法性。我们开展了一系列实验,以确定象牙样本中DNA最集中的位置,以及如何最好地提高可能因DNA浓度不同而有所差异的样本组的DNA产量。我们研究了以下因素对DNA扩增成功率的影响:所提取的象牙层(牙骨质和/或牙本质)、脱矿质温度和时间以及洗脱液浓度。由于粉碎后的样本脱矿质会产生沉淀和上清液,我们还评估了沉淀、上清液、它们的混合物的DNA扩增成功率,以及用于提取的各自用量的差异。我们的结果表明,象牙的外层牙骨质含有最高浓度的DNA,如有可能,应将其分离出来并专门用作提取象牙的原料。使用脱矿质裂解物的混合物可提高提取效率,在4°C下将脱矿质时间延长至3天或更长时间也有同样效果。对于低模板DNA象牙样本,其次是中等质量样本,改进最为显著。高质量样本的扩增成功率不受这些变化的影响。将这种优化方法应用于3068个象牙样本,结果显示,在16个微卫星位点中,至少有10个位点的两个等位基因得到确认的样本占81.2%(这是我们纳入DNA溯源分析的阈值)。