Columbia River Inter-Tribal Fish Commission, 3059 F National Fish Hatchery Rd, Hagerman, ID 83332, USA.
Mol Ecol Resour. 2012 Sep;12(5):942-9. doi: 10.1111/j.1755-0998.2012.03161.x. Epub 2012 Jun 15.
DNA sequence data were collected and screened for single nucleotide polymorphisms (SNPs) in westslope cutthroat trout (Oncorhynchus clarki lewisi) and also for substitutions that could be used to genetically discriminate rainbow trout (O. mykiss) and cutthroat trout, as well as several cutthroat trout subspecies. In total, 260 expressed sequence tag-derived loci were sequenced and allelic discrimination genotyping assays developed from 217 of the variable sites. Another 50 putative SNPs in westslope cutthroat trout were identified by restriction-site-associated DNA sequencing, and seven of these were developed into assays. Twelve O. mykiss SNP assays that were variable within westslope cutthroat trout and 12 previously published SNP assays were also included in downstream testing. A total of 241 assays were tested on six westslope cutthroat trout populations (N = 32 per population), as well as collections of four other cutthroat trout subspecies and a population of rainbow trout. All assays were evaluated for reliability and deviation from Hardy-Weinberg and linkage equilibria. Poorly performing and duplicate assays were removed from the data set, and the remaining 200 assays were used in tests of population differentiation. The remaining markers easily distinguished the various subspecies tested, as evidenced by mean G(ST) of 0.74. A smaller subset of the markers (N = 86; average G(ST) = 0.40) was useful for distinguishing the six populations of westslope cutthroat trout. This study increases by an order of magnitude the number of genetic markers available for the study of westslope cutthroat trout and closely related taxa and includes many markers in genes (developed from ESTs).
DNA 序列数据被收集并筛选出西落基山鳟鱼(Oncorhynchus clarki lewisi)的单核苷酸多态性(SNP),以及可用于遗传区分虹鳟(O. mykiss)和鳟鱼的替代物,以及几种鳟鱼亚种。总共测序了 260 个表达序列标签衍生的基因座,并从 217 个可变性位点中开发了等位基因区分基因型分析检测。通过相关 DNA 测序,还在西落基山鳟鱼中鉴定出了另外 50 个假定的 SNP,其中 7 个被开发成了分析检测。还包括了 12 个在西落基山鳟鱼中具有变异性的 O. mykiss SNP 分析检测和 12 个以前发表的 SNP 分析检测,用于下游测试。总共在 6 个西落基山鳟鱼群体(每个群体 32 个个体)以及其他 4 个鳟鱼亚种和一个虹鳟群体的采集物上测试了 241 个分析检测。所有的分析检测都评估了可靠性以及偏离 Hardy-Weinberg 和连锁平衡的情况。性能较差和重复的分析检测被从数据集中删除,其余 200 个分析检测被用于群体分化的测试。剩下的标记很容易区分出所测试的各种亚种,平均 G(ST)为 0.74。标记的一个较小子集(N = 86;平均 G(ST)为 0.40)可用于区分西落基山鳟鱼的 6 个群体。这项研究将可用于研究西落基山鳟鱼和密切相关类群的遗传标记数量增加了一个数量级,其中包括许多来自 ESTs 的基因中的标记。