Garrett Molly J, Nerkowski Stacey A, Kieran Shannon, Campbell Nathan R, Barbosa Soraia, Conway Courtney J, Hohenlohe Paul A, Waits Lisette P
Department of Fish and Wildlife Sciences, College of Natural Resources University of Idaho Moscow Idaho USA.
GTseek LLC Twin Falls Idaho USA.
Ecol Evol. 2024 May 20;14(5):e11321. doi: 10.1002/ece3.11321. eCollection 2024 May.
Minimally invasive samples are often the best option for collecting genetic material from species of conservation concern, but they perform poorly in many genomic sequencing methods due to their tendency to yield low DNA quality and quantity. Genotyping-in-thousands by sequencing (GT-seq) is a powerful amplicon sequencing method that can genotype large numbers of variable-quality samples at a standardized set of single nucleotide polymorphism (SNP) loci. Here, we develop, optimize, and validate a GT-seq panel for the federally threatened northern Idaho ground squirrel () to provide a standardized approach for future genetic monitoring and assessment of recovery goals using minimally invasive samples. The optimized panel consists of 224 neutral and 81 putatively adaptive SNPs. DNA collected from buccal swabs from 2016 to 2020 had 73% genotyping success, while samples collected from hair from 2002 to 2006 had little to no DNA remaining and did not genotype successfully. We evaluated our GT-seq panel by measuring genotype discordance rates compared to RADseq and whole-genome sequencing. GT-seq and other sequencing methods had similar population diversity and estimates, but GT-seq consistently called more heterozygotes than expected, resulting in negative values at the population level. Genetic ancestry assignment was consistent when estimated with different sequencing methods and numbers of loci. Our GT-seq panel is an effective and efficient genotyping tool that will aid in the monitoring and recovery of this threatened species, and our results provide insights for applying GT-seq for minimally invasive DNA sampling techniques in other rare animals.
对于从受保护物种中收集遗传物质而言,微创样本通常是最佳选择,但由于其往往会产生低质量和低数量的DNA,在许多基因组测序方法中表现不佳。测序数千分型法(GT-seq)是一种强大的扩增子测序方法,能够在一组标准化的单核苷酸多态性(SNP)位点对大量质量参差不齐的样本进行基因分型。在此,我们为联邦政府列为濒危物种的爱达荷州北部地松鼠()开发、优化并验证了一个GT-seq面板,以便为未来使用微创样本进行遗传监测和恢复目标评估提供标准化方法。优化后的面板由224个中性SNP和81个推定适应性SNP组成。2016年至2020年从口腔拭子收集的DNA的基因分型成功率为73%,而2002年至2006年从毛发收集的样本几乎没有剩余DNA,无法成功进行基因分型。我们通过测量与RADseq和全基因组测序相比的基因分型不一致率来评估我们的GT-seq面板。GT-seq和其他测序方法具有相似的群体多样性和估计值,但GT-seq始终比预期检出更多杂合子,导致群体水平上的值为负。使用不同测序方法和位点数量进行估计时,遗传血统分配是一致的。我们的GT-seq面板是一种有效且高效的基因分型工具,将有助于对这种濒危物种进行监测和恢复,我们的结果为在其他珍稀动物中应用GT-seq进行微创DNA采样技术提供了见解。