利用Pool-Seq在异源多倍体物种种群中高效发现核苷酸多态性

A. Hirao, Yoshihiko Onda, Rie Shimizu‐Inatsugi, J. Sese, K. Shimizu, T. Kenta
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引用次数: 2

摘要

异体多倍体物种的群体遗传学研究落后于二倍体物种,这是因为在分析来自杂交亲本物种的同源重复基因拷贝方面存在实际困难。Pool-Seq,即对汇集的个体进行大规模平行测序,在检测多个群体内部和群体之间的核苷酸多态性方面具有很高的潜力;然而,它的使用仅限于二倍体物种。我们将Pool-Seq应用于一个异源多倍体物种,通过建立一个生物信息学管道,将读取值分配到每个同源物以及每个同源物中的每个多态性等位基因。我们同时对来自24个群体的20个个体的8个基因进行了测序,并在每个同源物中发现了100多个多态性位点。对于两个位点,我们使用读取数来估计等位基因频率,然后通过基于个体的估计来验证这些估计。使用我们的生物信息学管道的Pool-Seq可以有效地评估大量个体的核苷酸多态性,甚至在异源多倍体物种中也是如此。
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Cost-Effective Discovery of Nucleotide Polymorphisms in Populations of an Allopolyploid Species Using Pool-Seq
Population genetics studies of allopolyploid species lag behind those of diploid species because of practical difficulties in analysis of homeologs-duplicated gene copies originating from hybridized parental species. Pool-Seq, i.e. massive parallel sequencing of pooled individuals, has high potential for detecting nucleotide polymorphisms within and among multiple populations; however, its use has been limited to diploid species. We applied Pool-Seq to an allopolyploid species by developing a bioinformatic pipeline that assigns reads to each homeolog as well as to each polymorphic allele within each homeolog. We simultaneously sequenced eight genes from twenty individuals from each of 24 populations, and found over 100 polymorphic sites in each homeolog. For two sites, we estimated allele frequencies using the number of reads and then validated these estimations by making individual-based estimations. Pool-Seq using our bioinformatic pipeline allows efficient evaluation of nucleotide polymorphisms in a large number of individuals, even in allopolyploid species.
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