Wang K, Zhuang J Y, Huang D R, Ying J Z, Fan Y Y
Chinese National Center for Rice Improvement/State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Chinese National Center for Rice Improvement/State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China
Genet Mol Res. 2015 Apr 10;14(2):3209-22. doi: 10.4238/2015.April.10.33.
Genome-wide re-sequencing of the Zhenshan 97 (ZS97) and Milyang 46 (MY46) parents of an elite three-line hybrid rice developed in China resulted in the generation of 9.91 G bases of data with an effective sequencing depth of 11.66x and 11.51x, respectively. Detection of genome-wide DNA polymorphisms, single nucleotide polymorphisms (SNPs), short insertions/deletions (InDels; 1-5 bp), and structural variations (SVs), which is an invaluable variation resource for genetic research and molecular marker-assisted breeding, was conducted by comparing whole-genome re-sequencing data. A total of 364,488 SNPs, 61,181 InDels and 6298 SVs were detected in ZS97 and 364,179 SNPs, 61,984 InDels and 6408 SVs were detected in MY46 compared to the 9311 reference sequence. Synteny analysis of the variation revealed a total of 77,013 identical and 181,737 different SNPs and 15,021 identical and 1205 different InDels between ZS97 and MY46, respectively. A total of 180 InDels 3-8 bp in length between ZS97 and MY46 were selected for experimental validation; 160 polymerase chain reaction products were efficiently separated on 6% non-denaturing polyacrylamide gels. Identification of genome-wide variation among the parents of the elite hybrid as well as the set of 160 polymerase chain reaction-based InDel markers will facilitate future genetic studies and the molecular breeding of hybrid rice.
对中国培育的一个优良三系杂交水稻的亲本珍汕 97(ZS97)和密阳 46(MY46)进行全基因组重测序,分别产生了 9.91 G 碱基的数据,有效测序深度分别为 11.66 倍和 11.51 倍。通过比较全基因组重测序数据,检测全基因组 DNA 多态性、单核苷酸多态性(SNP)、短插入/缺失(InDel;1 - 5 bp)和结构变异(SV),这些是遗传研究和分子标记辅助育种的宝贵变异资源。与 9311 参考序列相比,在 ZS97 中检测到总共 364,488 个 SNP、61,181 个 InDel 和 6298 个 SV,在 MY46 中检测到 364,179 个 SNP、61,984 个 InDel 和 6408 个 SV。变异的共线性分析显示,ZS97 和 MY46 之间分别共有 77,013 个相同和 181,737 个不同的 SNP,以及 15,021 个相同和 1205 个不同的 InDel。在 ZS97 和 MY46 之间选择了总共 180 个长度为 3 - 8 bp 的 InDel 进行实验验证;160 个聚合酶链反应产物在 6%非变性聚丙烯酰胺凝胶上有效分离。鉴定优良杂交亲本之间的全基因组变异以及这组基于聚合酶链反应的 160 个 InDel 标记将有助于未来杂交水稻的遗传研究和分子育种。