Fang Yanlong, Liu Shulin, Dong Quanzhong, Zhang Kaixin, Tian Zhixi, Li Xiyu, Li Wenbin, Qi Zhongying, Wang Yue, Tian Xiaocui, Song Jie, Wang Jiajing, Yang Chang, Jiang Sitong, Li Wen-Xia, Ning Hailong
Key Laboratory of Soybean Biology, Ministry of Education/Key Laboratory of Soybean Biology and Breeding/Genetics, Ministry of Agriculture, Northeast Agricultural University, Harbin, China.
State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Front Plant Sci. 2020 Feb 14;11:9. doi: 10.3389/fpls.2020.00009. eCollection 2020.
Plant height is an important target for soybean breeding. It is a typical quantitative trait controlled by multiple genes and is susceptible to environmental influences. Here, we carried out phenotypic analysis of 156 recombinant inbred lines derived from "Dongnong L13" and "Henong 60" in nine environments at four locations over 6 years using interval mapping and inclusive composite interval mapping methods. We performed quantitative trait locus (QTL) analysis by applying pre-built simple-sequence repeat maps. We detected 48 QTLs, including nine significant QTLs detected by multiple methods and in multiple environments. Meanwhile, genotyping of all lines using the SoySNP660k BeadChip produced 54,836 non-redundant single-nucleotide polymorphism (SNP) genotypes. We used five multi-locus genome-wide association analysis methods to locate 10 quantitative trait nucleotides (QTNs), four of which overlap with previously located QTLs. Five candidate genes related to plant height are predicted to lie within 200 kb of these four QTNs. We identified 19 homologous genes in Arabidopsis, two of which may be associated with plant height. These findings further our understanding of the multi-gene regulatory network and genetic determinants of soybean plant height, which will be important for breeding high-yielding soybean.
株高是大豆育种的一个重要目标。它是一个典型的受多基因控制的数量性状,易受环境影响。在此,我们利用区间作图和包容性复合区间作图方法,在6年时间里,于4个地点的9种环境下,对由“东农L13”和“合农60”衍生的156个重组自交系进行了表型分析。我们通过应用预先构建的简单序列重复图谱进行数量性状基因座(QTL)分析。我们检测到48个QTL,其中包括通过多种方法和在多种环境下检测到的9个显著QTL。同时,使用SoySNP660k BeadChip对所有品系进行基因分型,产生了54,836个非冗余单核苷酸多态性(SNP)基因型。我们使用五种多位点全基因组关联分析方法定位了10个数量性状核苷酸(QTN),其中四个与先前定位的QTL重叠。预计与株高相关的五个候选基因位于这四个QTN的200 kb范围内。我们在拟南芥中鉴定出19个同源基因,其中两个可能与株高有关。这些发现加深了我们对大豆株高多基因调控网络和遗传决定因素的理解,这对培育高产大豆具有重要意义。