Babiker E M, Gordon T C, Chao S, Rouse M N, Wanyera R, Newcomb M, Brown-Guedira G, Pretorius Z A, Bonman J M
Small Grains and Potato Germplasm Research Unit, USDA-ARS, 1691 S 2700 W, Aberdeen, ID, 83210, USA.
Cereal Crops Research Unit, USDA-ARS, 1605 Albrecht Blvd, Fargo, ND, 58102, USA.
Theor Appl Genet. 2016 Nov;129(11):2161-2170. doi: 10.1007/s00122-016-2764-5. Epub 2016 Aug 20.
A gene for Ug99 resistance from wheat landrace CItr 4311 was detected on the long arm of chromosome 2B. Wheat landrace CItr 4311 has seedling resistance to stem rust caused by Puccinia graminis f. sp. tritici race TTKSK and field resistance to the Ug99 race group. Parents, F seedlings, 121 doubled haploid (DH) lines, and 124 recombinant inbred lines (RILs) developed from a cross between CItr 4311 and the susceptible line LMPG-6 were evaluated for seedling resistance to race TTKSK. Goodness-of-fit tests indicated that a single dominant gene in CItr 4311 conditioned the TTKSK resistance. The 90 K wheat iSelect SNP platform was used to genotype parents and the DH population. The seedling resistance locus was mapped to the chromosome arm 2BL. Parents and the DH population were evaluated for field resistance in Kenya. One major QTL for the field resistance was consistently detected in the same region on 2BL as the seedling resistance. Using KASP assays, five linked SNP markers were used to verify the result in the 124 RIL, 35 wheat accessions, 46 DH lines from the LMPG-6/PI 165194 cross and F seedlings, and susceptible bulks derived from crosses between six resistant landraces with LMPG-6. Race specificity, mapping results, and haplotype similarity with lines with Sr9h (Gabo 56, Timstein, and PI 670015), support the hypothesis that the Sr gene in CItr 4311 and the landraces is Sr9h. The KASP assays developed in this study will be useful for pyramiding the TTKSK resistance from CItr 4311 with other Sr genes effective against Ug99.
从小麦地方品种CItr 4311中检测到一个抗Ug99的基因,位于2B染色体长臂上。小麦地方品种CItr 4311对由小麦条锈菌生理小种TTKSK引起的条锈病具有苗期抗性,对Ug99小种群体具有田间抗性。对CItr 4311与感病品系LMPG - 6杂交产生的亲本、F1代幼苗、121个双单倍体(DH)系和124个重组自交系(RIL)进行了苗期对TTKSK小种抗性的评估。拟合优度检验表明,CItr 4311中的一个显性单基因决定了对TTKSK的抗性。使用90K小麦iSelect SNP平台对亲本和DH群体进行基因分型。苗期抗性位点被定位到2BL染色体臂上。对亲本和DH群体在肯尼亚进行了田间抗性评估。在2BL上与苗期抗性相同的区域一致检测到一个主要的田间抗性QTL。使用竞争性等位基因特异性PCR(KASP)分析,五个连锁SNP标记用于在124个RIL、35个小麦种质、LMPG - 6/PI 165194杂交的46个DH系和F1代幼苗以及六个抗性地方品种与LMPG - 6杂交产生的感病混合群体中验证结果。与具有Sr9h的品系(Gabo 56、Timstein和PI 670015)的小种特异性、定位结果和单倍型相似性,支持了CItr 4311和地方品种中的Sr基因是Sr9h的假设。本研究中开发的KASP分析将有助于将CItr 4311对TTKSK的抗性与其他对Ug99有效的Sr基因聚合。