Department of Biology, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON, L5L 1C6, Canada.
Unidad de Recursos Naturales, Centro de Investigación Científica de Yucatán, Calle 43 No. 130, Col. Chuburná de Hidalgo, CP, 97205, Mérida, Yucatán, México.
Mol Ecol Resour. 2017 Nov;17(6):1122-1135. doi: 10.1111/1755-0998.12653. Epub 2017 Feb 18.
The spatial signature of microevolutionary processes structuring genetic variation may play an important role in the detection of loci under selection. However, the spatial location of samples has not yet been used to quantify this. Here, we present a new two-step method of spatial outlier detection at the individual and deme levels using the power spectrum of Moran eigenvector maps (MEM). The MEM power spectrum quantifies how the variation in a variable, such as the frequency of an allele at a SNP locus, is distributed across a range of spatial scales defined by MEM spatial eigenvectors. The first step (Moran spectral outlier detection: MSOD) uses genetic and spatial information to identify outlier loci by their unusual power spectrum. The second step uses Moran spectral randomization (MSR) to test the association between outlier loci and environmental predictors, accounting for spatial autocorrelation. Using simulated data from two published papers, we tested this two-step method in different scenarios of landscape configuration, selection strength, dispersal capacity and sampling design. Under scenarios that included spatial structure, MSOD alone was sufficient to detect outlier loci at the individual and deme levels without the need for incorporating environmental predictors. Follow-up with MSR generally reduced (already low) false-positive rates, though in some cases led to a reduction in power. The results were surprisingly robust to differences in sample size and sampling design. Our method represents a new tool for detecting potential loci under selection with individual-based and population-based sampling by leveraging spatial information that has hitherto been neglected.
微进化过程塑造遗传变异的空间特征可能在检测受选择影响的基因座中发挥重要作用。然而,目前还没有利用样本的空间位置来量化这一点。在这里,我们使用 Moran 特征向量图(MEM)的功率谱提出了一种新的两步法,用于在个体和居群水平上检测空间离群值。MEM 功率谱量化了一个变量(例如 SNP 基因座上的等位基因频率)的变化如何在由 MEM 空间特征向量定义的一系列空间尺度上分布。第一步(Moran 谱离群值检测:MSOD)使用遗传和空间信息,通过异常的功率谱识别异常基因座。第二步使用 Moran 谱随机化(MSR)来测试异常基因座与环境预测因子之间的关联,同时考虑空间自相关。我们使用来自两篇已发表论文的模拟数据,在不同的景观配置、选择强度、扩散能力和采样设计场景中测试了这种两步法。在包括空间结构的场景中,MSOD 单独足以在个体和居群水平上检测到离群基因座,而无需纳入环境预测因子。后续使用 MSR 通常会降低(已经很低)假阳性率,但在某些情况下会降低功效。结果对样本量和采样设计的差异非常稳健。我们的方法通过利用迄今被忽视的空间信息,代表了一种用于检测基于个体和基于群体采样的潜在选择基因座的新工具。