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首页> 外文期刊>Molecular Breeding >Genotyping-by-sequencing to remap QTL for type II Fusarium head blight and leaf rust resistance in a wheat-tall wheatgrass introgression recombinant inbred population
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Genotyping-by-sequencing to remap QTL for type II Fusarium head blight and leaf rust resistance in a wheat-tall wheatgrass introgression recombinant inbred population

机译:通过测序进行基因分型以重定位小麦高麦草渗入重组近交群体中II型镰刀菌的枯萎病和抗叶锈病的QTL

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摘要

Fusarium graminearum Schwabe (Fusarium head blight, FHB) and Puccinia triticina Eriks (leaf rust) are two major fungal pathogens posing a continuous threat to the wheat crop; consequently, identifying resistance genes from various sources is always of importance to wheat breeders. We identified tightly linked single nucleotide polymorphism (SNP) markers for the FHB resistance quantitative trait locus (QTL) Qfhs. pur-7EL and the leaf rust resistance locus Lr19 using genotyping-by-sequencing (GBS) in a wheat-tall wheatgrass introgression-derived recombinant inbred line (RIL) population. One thousand and seven hundred high-confidence SNPs were used to conduct the linkage and QTL analysis. Qfhs. pur-7EL was mapped to a 2.9 cM region containing four markers within a 43.6 cM segment of wheatgrass chromosome 7el(2) that was translocated onto wheat chromosome 7DL. Lr19 from 7el(1) was mapped to a 1.21 cM region containing two markers in the same area, in repulsion. Five lines were identified with the resistance-associated SNP alleles for Qfhs. pur-7EL and Lr19 in coupling. Two SNP markers in the Qfhs. pur-7EL region were converted into PCR-based KASP markers. Investigation of the genetic characteristics of the parental lines of this RIL population indicated that they are translocation lines in two different wheat cultivar genetic backgrounds instead of 7E-7D substitution lines in Thatcher wheat background, as previously reported in the literature.
机译:镰刀镰刀菌(Fusarium head b枯病,FHB)和小麦锈菌(Puccinia triticina Eriks)(叶锈病)是对小麦作物造成持续威胁的两种主要真菌病原体。因此,鉴定来自各种来源的抗性基因对小麦育种者总是很重要。我们为FHB抗性定量性状基因座(QTL)Qfhs确定了紧密连接的单核苷酸多态性(SNP)标记。 pur-7EL和抗叶锈病基因座Lr19,采用基因分型(GBS)技术,在小麦高小麦草渗入性重组近交系(RIL)群体中进行。使用177个高可信度SNP进行连锁和QTL分析。 Qfhs。 pur-7EL被定位到一个2.9 cM区域,该区域在小麦草染色体7el(2)的43.6 cM区段内包含四个标记,该标记被转移到小麦7DL染色体上。排斥反应中来自7el(1)的Lr19定位到1.21 cM区域,该区域在同一区域中包含两个标记。与Qfhs的抗性相关SNP等位基因鉴定出5条品系。 pur-7EL和Lr19耦合。 Qfhs中有两个SNP标记。 pur-7EL区被转化为基于PCR的KASP标记。对这一RIL群体亲本系遗传特性的调查表明,它们是两个不同小麦品种遗传背景下的易位系,而不是撒切尔小麦背景中的7E-7D替代系,如先前文献报道。

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