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SNP Discovery and QTL Mapping of Sclerotinia Basal Stalk Rot Resistance in Sunflower using Genotyping-by-Sequencing

机译:应用测序基因分型的向日葵核盘菌基茎腐烂抗性的SNP发现和QTL定位

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Basal stalk rot (BSR), caused by the ascomycete fungus?Sclerotinia sclerotiorum?(Lib.) de Bary, is a serious disease of sunflower (Helianthus annuus?L.) in the cool and humid production areas of the world. Quantitative trait loci (QTL) for BSR resistance were identified in a sunflower recombinant inbred line (RIL) population derived from the cross HA 441 × RHA 439. A genotyping-by-sequencing (GBS) approach was adapted to discover single nucleotide polymorphism (SNP) markers. A genetic linkage map was developed comprised of 1053 SNP markers on 17 linkage groups (LGs) spanning 1401.36 cM. The RILs were tested in five environments (locations and years) for resistance to BSR. Quantitative trait loci were identified in each environment separately and also with integrated data across environments. A total of six QTL were identified in all five environments: one of each on LGs 4, 9, 10, 11, 16, and 17. The most significant QTL,?Qbsr-10.1?and?Qbsr-17.1, were identified at multiple environments on LGs 10 and 17, explaining 31.6 and 20.2% of the observed phenotypic variance, respectively. The remaining four QTL,?Qbsr-4.1,?Qbsr-9.1,?Qbsr-11.1, and?Qbsr-16.1, were detected in only one environment on LGs 4, 9, 11, and 16, respectively. Each of these QTL explains between 6.4 and 10.5% of the observed phenotypic variation in the RIL population. Alleles conferring increased resistance were contributed by both parents. The potential of the?Qbsr-10.1?and?Qbsr-17.1?in marker-assisted selection (MAS) breeding are discussed.
机译:由子囊菌真菌核盘菌(Sclerotinia sclerotiorum)(Lib。)de Bary引起的基茎腐烂(BSR)是世界上阴凉潮湿的产区的一种严重的向日葵(Helianthus annuus?L。)病。在来源于杂交HA 441×RHA 439的向日葵重组近交系(RIL)群体中鉴定了BSR抗性的定量性状基因座(QTL)。采用测序的基因分型(GBS)方法发现单核苷酸多态性(SNP) )标记。建立了遗传连锁图谱,该遗传连锁图谱由跨越1401.36 cM的17个连锁组(LG)上的1053个SNP标记组成。在五个环境(位置和年份)中测试了RIL对BSR的抵抗力。在每个环境中分别确定了数量性状基因座,并且还使用了跨环境的集成数据。在所有五个环境中总共确定了六个QTL:在LG 4、9、10、11、16和17上每个都确定了一个。最重要的QTL(Qbsr-10.1)和Qbsr-17.1在多个位置上被确定。 LG 10和LG 17上的环境分别解释了观察到的表型变异的31.6%和20.2%。分别在LG 4、9、11和16的仅一个环境中检测到其余四个QTL,即Qbsr-4.1,Qbsr-9.1,Qbsr-11.1和Qbsr-16.1。这些QTL中的每个解释了RIL群体中观察到的表型变异的6.4%至10.5%。赋予抗性的等位基因由父母双方共同贡献。讨论了Qbsr-10.1和Qbsr-17.1在标记辅助选择(MAS)育种中的潜力。

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