首页> 外文期刊>BMC Genomics >Development of a high-density linkage map and mapping of the three-pistil gene ( Pis1 ) in wheat using GBS markers
【24h】

Development of a high-density linkage map and mapping of the three-pistil gene ( Pis1 ) in wheat using GBS markers

机译:使用GBS标记开发小麦高密度连锁图谱和小麦三雌蕊基因(Pis1)的图谱

获取原文
           

摘要

Background The wheat mutant line three-pistil (TP) exhibits three pistils per floret. As TP normally has two or three seeds in each of the florets on the same spike, there is the possibility of increasing the number of grains per spike. Therefore, TP is a highly valuable mutant for breeding and for the study of floral development in wheat. To map the three-pistil gene ( Pis1 ), genotyping-by-sequencing single-nucleotide polymorphism (GBS-SNP) data from an F2 mapping population (CM28?×?CM28TP) was used to construct a genetic map that is of significant value. Results In the present study, a high-density genetic map of wheat containing 2917 GBS-SNP markers was constructed. Twenty-one linkage groups were resolved, with a total length of 2371.40?cM. The individual chromosomes range from 2.64?cM to 454.55?cM with an average marker density of 0.81?cM. The Pis1 gene was mapped using this high-resolution map, and two flanking SNP markers tightly linked to the gene, M70 and M71 , were identified. The Pis1 is 3.00?cM from M70 and 1.10?cM from M71 . In bread wheat genome, M70 and M71 were found to delimit a physical distance of 3.40?Mb, which encompasses 127 protein-coding genes. To validate the GBS-generated genotypic data and to eliminate missing marker data in the Pis1 region, five Kompetitive Allele-Specific PCR (KASP) assays were designed from corresponding GBS sequences, which harbor SNPs that surround Pis1 . Three KASP-SNP markers, KM70 , KM71 , and KM75 , were remapped to the Pis1 gene region. Conclusions This work not only lays the foundation for the map-based cloning of Pis1 but can also serve as a valuable tool for studying marker-trait association of important traits and marker-assisted breeding in wheat.
机译:背景技术小麦突变体三雌蕊(TP)表现出每个小花三个雌蕊。由于TP通常在同一穗上的每个小花中都有两个或三个种子,因此有可能增加每个穗上的谷粒数量。因此,TP是小麦育种和花卉发育研究的极有价值的突变体。为了绘制三个雌蕊基因(Pis1),使用F 2 作图群体(CM28?×?CM28TP)的单核苷酸多态性(GBS-SNP)测序进行基因分型。具有重要价值的遗传图谱。结果在本研究中,构建了包含2917 GBS-SNP标记的小麦高密度遗传图谱。解决了二十一个连锁基团,总长度为2371.40?cM。单个染色体的范围从2.64?cM到454.55?cM,平均标记密度为0.81?cM。使用该高分辨率图谱绘制了Pis1基因,并鉴定了与该基因M70和M71紧密相关的两个侧翼SNP标记。 Pis1从M70开始为3.00?cM,从M71开始为1.10?cM。在面包小麦基因组中,发现M70和M71的物理距离为3.40?Mb,其中包括127个蛋白质编码基因。为了验证GBS生成的基因型数据并消除Pis1区域中缺失的标记数据,从相应的GBS序列中设计了五种竞争性等位基因特异性PCR(KASP)检测法,这些检测法包含环绕Pis1的SNP。将三个KASP-SNP标记KM70,KM71和KM75重新映射到Pis1基因区域。结论这项工作不仅为基于Pis1的图谱克隆奠定了基础,而且可以作为研究小麦重要性状的标记-性状关联和标记辅助育种的有价值的工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号