Hawai'i Institute of Marine Biology, University of Hawai'i at Mānoa, Kāne'ohe, Hawai'i, United States of America.
PLoS One. 2012;7(3):e34241. doi: 10.1371/journal.pone.0034241. Epub 2012 Mar 28.
The field of phylogeography has long since realized the need and utility of incorporating nuclear DNA (nDNA) sequences into analyses. However, the use of nDNA sequence data, at the population level, has been hindered by technical laboratory difficulty, sequencing costs, and problematic analytical methods dealing with genotypic sequence data, especially in non-model organisms. Here, we present a method utilizing the 454 GS-FLX Titanium pyrosequencing platform with the capacity to simultaneously sequence two species of sea star (Meridiastra calcar and Parvulastra exigua) at five different nDNA loci across 16 different populations of 20 individuals each per species. We compare results from 3 populations with traditional Sanger sequencing based methods, and demonstrate that this next-generation sequencing platform is more time and cost effective and more sensitive to rare variants than Sanger based sequencing. A crucial advantage is that the high coverage of clonally amplified sequences simplifies haplotype determination, even in highly polymorphic species. This targeted next-generation approach can greatly increase the use of nDNA sequence loci in phylogeographic and population genetic studies by mitigating many of the time, cost, and analytical issues associated with highly polymorphic, diploid sequence markers.
系统发生地理学领域早就认识到需要并利用核 DNA(nDNA)序列进行分析。然而,在群体水平上使用 nDNA 序列数据受到技术实验室困难、测序成本以及处理基因型序列数据的有问题的分析方法的阻碍,特别是在非模式生物中。在这里,我们提出了一种利用 454 GS-FLX Titanium 焦磷酸测序平台的方法,该平台能够同时对两种海星(Meridiastra calcar 和 Parvulastra exigua)在五个不同的 nDNA 基因座进行测序,每个物种有 16 个不同的种群,每个种群有 20 个个体。我们比较了来自 3 个种群的结果与传统的基于 Sanger 测序的方法,并证明这种下一代测序平台比基于 Sanger 的测序方法更省时、更经济、对稀有变异更敏感。一个关键的优势是,克隆扩增序列的高覆盖率简化了单倍型的确定,即使在高度多态的物种中也是如此。这种靶向的下一代方法可以大大增加 nDNA 序列标记在系统发生和种群遗传研究中的应用,减轻与高度多态性、二倍体序列标记相关的许多时间、成本和分析问题。