Guan Xuanli, Yuyama Nana, Stewart Alan, Ding Chenglong, Xu Nengxiang, Kiyoshi Takako, Cai Hongwei
Department of Plant Genetics, Breeding and Seed Science, College of Agronomy and Biotechnology, China Agricultural UniversityBeijing, China.
Laboratory of Crop Heterosis and Utilization, Ministry of EducationBeijing, China.
Front Plant Sci. 2017 Apr 21;8:584. doi: 10.3389/fpls.2017.00584. eCollection 2017.
To assess the genetic diversity and population structure of species, we used 32 nuclear simple sequence repeat (SSR) markers and 7 cytoplasmic gene markers to analyze a total of 357 individuals from 162 accessions of 9 species. This survey revealed a high level of polymorphism, with an average number of alleles per locus of 23.59 and 5.29 and an average PIC-value of 0.83 and 0.54 for nuclear SSR markers and cytoplasmic gene markers, respectively. Analysis of molecular variance (AMOVA) revealed that 16.27 and 16.53% of the total variation was due to differences among species, with the remaining 56.35 and 83.47% due to differences within species and 27.39 and 0% due to differences within individuals in 32 nuclear SSR markers set and 6 chloroplast gene markers set, respectively. The 32 nuclear SSR markers detected three subpopulations among 357 individuals, whereas the 6 chloroplast gene markers revealed three subpopulations among 160 accessions in the STRUCTURE analysis. In the clustering analysis, the three inbred species clustered into a single group, whereas the outbreeding species were clearly divided, especially according to nuclear SSR markers. In addition, almost all populations were clustered into group C4, which could be further divided into three subgroups, whereas populations primarily clustered into two groups (C2 and C3), with a few lines that instead grouped with (C4) or (C6). Together, these results will useful for the use of germplasm for improvement and increase the effectiveness of ryegrass breeding.
为评估物种的遗传多样性和群体结构,我们使用了32个核简单序列重复(SSR)标记和7个细胞质基因标记,对9个物种的162份种质资源中的357个个体进行了分析。这项调查揭示了高水平的多态性,核SSR标记和细胞质基因标记的每个位点平均等位基因数分别为23.59和5.29,平均PIC值分别为0.83和0.54。分子方差分析(AMOVA)显示,在32个核SSR标记组和6个叶绿体基因标记组中,总变异的16.27%和16.53%分别归因于物种间差异,其余56.35%和83.47%归因于物种内差异,27.39%和0%归因于个体内差异。32个核SSR标记在357个个体中检测到三个亚群,而6个叶绿体基因标记在STRUCTURE分析中的160份种质资源中揭示了三个亚群。在聚类分析中,三个自交物种聚为一组,而异交物种则明显分开,尤其是根据核SSR标记。此外,几乎所有群体都聚为C4组,该组可进一步分为三个亚组,而群体主要聚为两组(C2和C3),少数品系则与(C4)或(C6)归为一组。总之,这些结果将有助于利用种质资源进行改良,并提高黑麦草育种的有效性。