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Identification Mapping and Molecular Marker Development for Rgsr8.1: A New Quantitative Trait Locus Conferring Resistance to Gibberella Stalk Rot in Maize (Zea mays L.)

机译:Rgsr8.1的鉴定作图和分子标记开发:赋予玉米抗赤霉病茎秆新抗性的定量性状基因座

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摘要

Maize stalk rot is a major fungal disease worldwide, and is difficult to control by chemical methods. Therefore, in maize breeding, quantitative trait loci (QTLs) conferring resistance are important for controlling the disease. Next-generation sequencing technologies are considered a rapid and efficient method to establish the association of agronomic traits with molecular markers or candidate genes. In the present study, we employed QTL-seq, which is a whole-genome resequencing-based approach, to identify candidate genomic regions conferring resistance to maize stalk rot. A novel resistance QTL Rgsr8.1 was finely mapped, conferring broad-spectrum resistance to Gibberella stalk rot (GSR). Segregation analysis in F2 and BC1F1 populations, which were derived from a cross between 18327 (Susceptible) and (Resistant), indicated that the resistance to GSR was likely to be a quantitatively inherited trait in maize. The result of QTL-seq showed that the resistance to GSR was mapped on chromosome 8 from 161.001 to 170.6 Mb. Based on the simple sequence repeat (SSR) markers, single-nucleotide polymorphism (SNP) markers, and the recombinant test, the location of Rgsr8.1 was narrowed down to 2.04 Mb, flanked by SSR-65 and SNP-25 markers at the physical location from 164.69 to 166.72 Mb based on the maize reference genome. In this region, two candidate resistant genes were found with, one auxin-responsive elements and the other encoding a disease resistance protein. In summary, these results will be useful in maize breeding programs to improve the resistance to GSR in maize.
机译:玉米秸秆腐烂是全世界主要的真菌病,很难用化学方法控制。因此,在玉米育种中,赋予抗性的数量性状位点(QTL)对于控制该病很重要。下一代测序技术被认为是建立农艺性状与分子标记或候选基因关联的一种快速有效的方法。在本研究中,我们采用基于全基因组重测序的方法QTL-seq来鉴定赋予玉米秸秆腐烂抗性的候选基因组区域。精细绘制了新的抗性QTL Rgsr8.1,赋予了对赤霉菌茎腐病(GSR)的广谱抗性。对F2和BC1F1群体的隔离分析源自18327(易感性)和(抗性)之间的杂交,表明对GSR的抗性很可能是玉米的数量遗传性状。 QTL-seq的结果表明,对GSR的抗性从161.001到170.6 Mb位于8号染色体上。基于简单序列重复(SSR)标记,单核苷酸多态性(SNP)标记和重组测试,Rgsr8.1的位置缩小到2.04 Mb,在Sg-65和SNP-25标记两侧基于玉米参考基因组的164.69至166.72 Mb的物理位置。在该区域,发现了两个候选抗性基因,其中一个生长素应答元件,另一个编码抗病蛋白。总而言之,这些结果将对玉米育种计划有用,以提高玉米对GSR的抗性。

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