Bio-Evaluation Center, Korea Research Institute of Bioscience and Biotechnology, Cheongwon, Chungbuk 363-883, Republic of Korea.
Theor Appl Genet. 2013 Apr;126(4):1103-19. doi: 10.1007/s00122-012-2039-8. Epub 2013 Jan 10.
Despite the intensive soybean [Glycine max (L.) Merrill] genome studies, the high chromosome number (20) of the soybean plant relative to many other major crops has hindered the development of a high-resolution genomewide genetic map derived from a single population. Here, we report such a map, which was constructed in an F15 population derived from a cross between G. max and G. soja lines using indel polymorphisms detected via a G. soja genome resequencing. By targeting novel indel markers to marker-poor regions, all marker intervals were reduced to under 6 cM on a genome scale. Comparison of the Williams 82 soybean reference genome sequence and our genetic map indicated that marker orders of 26 regions were discrepant with each other. In addition, our comparison showed seven misplaced and two absent markers in the current Williams 82 assembly and six markers placed on the scaffolds that were not incorporated into the pseudomolecules. Then, we showed that, by determining the missing sequences located at the presumed beginning points of the five major discordant segments, these observed discordant regions are mostly errors in the Williams 82 assembly. Distributions of the recombination rates along the chromosomes were similar to those of other organisms. Genotyping of indel markers and genome resequencing of the two parental lines suggested that some marker-poor chromosomal regions may represent introgression regions, which appear to be prevalent in soybean. Given the even and dense distribution of markers, our genetic map can serve as a bridge between genomics research and breeding programs.
尽管对大豆 [Glycine max (L.) Merrill] 基因组进行了深入研究,但相对于许多其他主要作物,大豆植物的高染色体数(20 条)阻碍了基于单一群体的高分辨率全基因组遗传图谱的发展。在这里,我们报告了这样一张图谱,它是通过大豆基因组重测序检测到的插入缺失多态性,在 G. max 和 G. soja 系杂交产生的 F15 群体中构建的。通过将新的插入缺失标记物靶向到标记物稀少的区域,所有标记物的间隔在基因组尺度上都缩小到了 6cM 以下。Williams 82 大豆参考基因组序列与我们的遗传图谱的比较表明,26 个区域的标记物顺序彼此不一致。此外,我们的比较表明,当前的 Williams 82 组装中存在七个错位和两个缺失的标记物,以及六个标记物位于未整合到假分子中的支架上。然后,我们表明,通过确定位于五个主要不一致片段假定起点处的缺失序列,这些观察到的不一致区域大多是 Williams 82 组装中的错误。染色体上重组率的分布与其他生物相似。插入缺失标记物的基因型分析和两个亲本系的基因组重测序表明,一些标记物稀少的染色体区域可能代表渗入区域,这些区域在大豆中似乎很普遍。鉴于标记物的均匀和密集分布,我们的遗传图谱可以作为基因组学研究和育种计划之间的桥梁。