作物学报 ›› 2023, Vol. 49 ›› Issue (2): 310-320.doi: 10.3724/SP.J.1006.2023.24015
杨硕1,3(
), 武阳春4, 刘鑫磊2, 唐晓飞2, 薛永国2, 曹旦2, 王婉3, 刘亭萱3, 祁航3, 栾晓燕2,*, 邱丽娟1,3,*(
)
YANG Shuo1,3(
), WU Yang-Chun4, LIU Xin-Lei2, TANG Xiao-Fei2, XUE Yong-Guo2, CAO Dan2, WANG Wan3, LIU Ting-Xuan3, QI Hang3, LUAN Xiao-Yan2,*, QIU Li-Juan1,3,*(
)
摘要:
蛋白质含量是大豆重要的品质性状, 受多基因控制, 定位大豆蛋白质含量相关位点并挖掘候选基因, 对定向培育高蛋白含量大豆品种具有重要意义。本研究以优良品种黑农88作为母本与高蛋白优异种质P73-6B作为父本杂交, 构建了一个由265个单株组成的F2群体, 利用中豆芯1号对F2群体进行基因型鉴定并构建图谱, 结合蛋白质含量表型数据, 采用IciMapping 4.2软件在20号染色体上定位了一个QTL, 物理距离为2.46 Mb, 在区间附近筛选出11个多态性SSR标记并分析群体, 将定位区间从2.46 Mb缩小至100.8 kb。增加Gm20_28349696、Gm20_30805913、Gm20_31341532和Gm20_31483719共4个SNP位点, 进一步将区间缩小到95.8 kb。对区间内包含的4个基因的9个不同组织在Phytozome v13.1和PPRD RNA-seq 2个数据库中的表达量分析得到了2个候选基因, 分别为Glyma.20g081800和Glyma.20g082000基因, 本试验结果为大豆蛋白质含量基因克隆及蛋白质调控机制研究提供了理论基础, 为大豆高蛋白分子标记育种提供材料和技术支撑。
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