Yang Yia, La Thang C, Gillman Jason D, Lyu Zhen, Joshi Trupti, Usovsky Mariola, Song Qijian, Scaboo Andrew
Division of Plant Science and Technology, University of Missouri, Columbia, MO, United States.
Plant Genetics Research Unit, United States Department of Agriculture-Agricultural Research Service, Columbia, MO, United States.
Front Plant Sci. 2022 Jul 29;13:938100. doi: 10.3389/fpls.2022.938100. eCollection 2022.
Modern soybean [] cultivars have low overall genetic variation due to repeated bottleneck events that arose during domestication and from selection strategies typical of many soybean breeding programs. In both public and private soybean breeding programs, the introgression of wild soybean () alleles is a viable option to increase genetic diversity and identify new sources for traits of value. The objectives of our study were to examine the genetic architecture responsible for seed protein and oil using a recombinant inbred line (RIL) population derived from hybridizing a line ('Osage') with a accession (PI 593983). Linkage mapping identified a total of seven significant quantitative trait loci on chromosomes 14 and 20 for seed protein and on chromosome 8 for seed oil with LOD scores ranging from 5.3 to 31.7 for seed protein content and from 9.8 to 25.9 for seed oil content. We analyzed 3,015 single F soybean plants to develop two residual heterozygotes derived near isogenic lines (RHD-NIL) populations by targeting nine SNP markers from genotype-by-sequencing, which corresponded to two novel quantitative trait loci (QTL) derived from : one for a novel seed oil QTL on chromosome 8 and another for a novel protein QTL on chromosome 14. Single marker analysis and linkage analysis using 50 RHD-NILs validated the chromosome 14 protein QTL, and whole genome sequencing of RHD-NILs allowed us to reduce the QTL interval from ∼16.5 to ∼4.6 Mbp. We identified two genomic regions based on recombination events which had significant increases of 0.65 and 0.72% in seed protein content without a significant decrease in seed oil content. A new Kompetitive allele-specific polymerase chain reaction (KASP) assay, which will be useful for introgression of this trait into modern elite cultivars, was developed in one region. Within the significantly associated genomic regions, a total of eight genes are considered as candidate genes, based on the presence of gene annotations associated with the protein or amino acid metabolism/movement. Our results provide better insights into utilizing wild soybean as a source of genetic diversity for soybean cultivar improvement utilizing native traits.
由于驯化过程中出现的反复瓶颈事件以及许多大豆育种计划典型的选择策略,现代大豆品种的总体遗传变异较低。在公共和私人大豆育种计划中,导入野生大豆(Glycine soja)等位基因是增加遗传多样性和确定有价值性状新来源的可行选择。我们研究的目的是利用一个重组自交系(RIL)群体来研究种子蛋白质和油含量的遗传结构,该群体由一个栽培品种(‘Osage’)与一个野生大豆材料(PI 593983)杂交产生。连锁图谱分析在14号和20号染色体上共鉴定出7个与种子蛋白质相关的显著数量性状位点,在8号染色体上鉴定出1个与种子油相关的显著数量性状位点,种子蛋白质含量的LOD值范围为5.3至31.7,种子油含量的LOD值范围为9.8至25.9。我们分析了3015株单粒F大豆植株,通过对基因型测序得到的9个SNP标记进行靶向分析,开发了两个剩余杂合近等基因系(RHD-NIL)群体,这两个群体对应于来自野生大豆的两个新的数量性状位点(QTL):一个是8号染色体上的一个新的种子油QTL,另一个是14号染色体上的一个新的蛋白质QTL。使用50个RHD-NIL进行的单标记分析和连锁分析验证了14号染色体上的蛋白质QTL,对RHD-NIL进行全基因组测序使我们能够将QTL区间从约16.5 Mbp缩小到约4.6 Mbp。我们基于重组事件确定了两个基因组区域,其种子蛋白质含量显著增加了0.65%和0.72%,而种子油含量没有显著降低。在其中一个区域开发了一种新的竞争性等位基因特异性聚合酶链反应(KASP)检测方法,该方法将有助于将该性状导入现代优良大豆品种。在显著相关的基因组区域内,基于与蛋白质或氨基酸代谢/转运相关的基因注释的存在,共有8个基因被视为候选基因。我们的研究结果为利用野生大豆作为遗传多样性来源改良大豆品种的本土性状提供了更好的见解。