College of Agriculture, The Analysis and Testing Center of College of Agriculture, Henan University of Science and Technology, 263 Kaiyuan Avenue, Luoyang, 471000, Henan Province, China.
Institute of Crop Sciences, State Key Laboratory of Crop Gene Resources and Breeding, National Wheat Improvement Centre, Chinese Academy of Agricultural Sciences (CAAS), 12 Zhongguancun South Street, Beijing, 100081, China.
Theor Appl Genet. 2024 Nov 6;137(12):261. doi: 10.1007/s00122-024-04769-9.
A major stable QTL, QGPC.caas-7AL, for grain protein content of wheat, was narrowed down to a 1.82-Mb inter on chromosome 7AL, and four candidate genes were predicated. Wheat grain protein content (GPC) is important for end-use quality. Identification of genetic loci for GPC is helpful to create new varieties with good processing quality and nutrients. Zhongmai 578 (ZM578) and Jimai 22 (JM22) are two elite wheat varieties with different contents of GPC. In the present study, 262 recombinant inbred lines (RILs) derived from a cross between ZM578 and JM22 were used to map the GPC with high-density wheat Illumina iSelect 50 K single-nucleotide polymorphism (SNP) array. Seven quantitative trait loci (QTLs) were identified for GPC on chromosomes 3AS, 3AL, 3BS, 4AL, 5BS, 5DL and 7AL by inclusive composite interval mapping, designated as QGPC.caas-3AS, QGPC.caas-3AL, QGPC.caas-3BS, QGPC.caas-4AL, QGPC.caas-5BS, QGPC.caas-5DL and QGPC.caas-7AL, respectively. Among these, alleles for increasing GPC at QGPC.caas-3AS, QGPC.caas-3BS, QGPC.caas-4AL and QGPC.caas-7AL loci were contributed by ZM578, whereas those at the other three loci were from JM22. The stable QTL QGPC.caas-7AL was fine mapped to a 1.82-Mb physical interval using secondary populations from six heterozygous recombinant plants obtained by selfing a residual RIL. Four genes were predicted as candidates of QGPC.caas-7AL based on sequence polymorphism and expression patterns. The near-isogenic lines (NILs) with the favorable allele at the QGPC.caas-7AL locus increased Farinograph stability time, Extensograph extension area, extensibility and maximum resistance by 19.6%, 6.3%, 6.0% and 20.3%, respectively. Kompetitive allele-specific PCR (KASP) marker for QGPC.caas-7AL was developed and validated in a diverse panel of 166 Chinese wheat cultivars. These results provide further insight into the genetic basis of GPC, and the fine-mapped QGPC.caas-7AL will be an attractive target for map-based cloning and marker-assisted selection in wheat breeding programs.
一个控制小麦籽粒蛋白质含量的主效稳定 QTL,QGPC.caas-7AL,被缩小到 7AL 染色体上的一个 1.82-Mb 区间内,并预测了四个候选基因。小麦籽粒蛋白质含量(GPC)对加工品质和营养价值很重要。鉴定 GPC 的遗传位点有助于创造具有良好加工品质和营养价值的新品种。中麦 578(ZM578)和济麦 22(JM22)是两个 GPC 含量不同的优质小麦品种。本研究利用 ZM578 和 JM22 杂交衍生的 262 个重组自交系(RIL),利用高密度小麦 Illumina iSelect 50K 单核苷酸多态性(SNP)芯片对 GPC 进行了作图。通过包容性复合区间作图法,在染色体 3AS、3AL、3BS、4AL、5BS、5DL 和 7AL 上鉴定到 7 个控制 GPC 的数量性状位点(QTL),分别命名为 QGPC.caas-3AS、QGPC.caas-3AL、QGPC.caas-3BS、QGPC.caas-4AL、QGPC.caas-5BS、QGPC.caas-5DL 和 QGPC.caas-7AL。其中,QGPC.caas-3AS、QGPC.caas-3BS、QGPC.caas-4AL 和 QGPC.caas-7AL 位点增加 GPC 的等位基因来自 ZM578,而其他三个位点的等位基因来自 JM22。利用自交一个剩余 RIL 获得的 6 个杂合重组植株的次级群体,将稳定的 QTL QGPC.caas-7AL 精细定位到一个 1.82-Mb 的物理区间。根据序列多态性和表达模式,预测了 4 个基因作为 QGPC.caas-7AL 的候选基因。具有 QGPC.caas-7AL 有利等位基因的近等基因系(NILs)分别使粉质仪稳定时间、拉伸仪延伸面积、拉伸性和最大阻力增加 19.6%、6.3%、6.0%和 20.3%。开发并验证了 QGPC.caas-7AL 的竞争性等位基因特异性 PCR(KASP)标记,在 166 个中国小麦品种的多样性面板中进行了验证。这些结果进一步揭示了 GPC 的遗传基础,精细定位的 QGPC.caas-7AL 将成为小麦育种计划中基于图谱克隆和标记辅助选择的一个有吸引力的目标。