de Jong Menno J, Lovatt Fiona, Hoelzel A Rus
Department of Biosciences, Durham University, Durham, UK.
Mol Ecol. 2021 Apr;30(7):1642-1658. doi: 10.1111/mec.15837. Epub 2021 Mar 2.
Founder populations are of special interest to both evolutionary and conservation biologists, but the detection of genetic signals of selection in these populations is challenging due to their demographic history. Geographically separated founder populations likely to have been subjected to similar selection pressures provide an ideal but rare opportunity to overcome these challenges. Here we take advantage of such a situation generated when small, isolated founder populations of reindeer were established on the island of South Georgia, and using this system we look for empirical evidence of selection overcoming strong genetic drift. We generated a 70 k ddRADseq single nucleotide polymorphism database for the two parallel reindeer founder populations and screened for signatures of soft sweeps. We find evidence for a genomic region under selection shared among the two populations, and support our findings with Wright-Fisher model simulations to assess the power and specificity of interpopulation selection scans-namely Bayescan, OutFLANK, PCadapt and a newly developed scan called Genome Wide Differentiation Scan (GWDS)-in the context of pairwise source-founder comparisons. Our simulations indicate that loci under selection in small founder populations are most probably detected by GWDS, and strengthen the hypothesis that the outlier region represents a true locus under selection. We explore possible, relevant functional roles for genes in linkage with the detected outlier loci.
奠基者群体对进化生物学家和保护生物学家都具有特殊意义,但由于其种群历史,在这些群体中检测选择的遗传信号具有挑战性。地理上隔离的奠基者群体可能受到相似的选择压力,这提供了一个克服这些挑战的理想但罕见的机会。在这里,我们利用了南乔治亚岛建立小型、孤立的驯鹿奠基者群体时产生的这种情况,并使用这个系统寻找选择克服强遗传漂变的经验证据。我们为两个平行的驯鹿奠基者群体生成了一个70k的ddRADseq单核苷酸多态性数据库,并筛选了软扫荡的特征。我们发现了两个群体之间共享的一个受选择的基因组区域的证据,并用赖特-费希尔模型模拟来支持我们的发现,以评估群体间选择扫描(即贝叶斯扫描、OutFLANK、PCadapt和一种新开发的称为全基因组分化扫描(GWDS))在成对源-奠基者比较中的功效和特异性。我们的模拟表明,在小型奠基者群体中受选择的位点最有可能被GWDS检测到,并强化了异常区域代表一个真正的受选择位点的假设。我们探索了与检测到的异常位点连锁的基因可能的相关功能作用。