首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Identification and assessment of two major QTLs for dwarf bunt resistance in winter wheat line 'IDO835'
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Identification and assessment of two major QTLs for dwarf bunt resistance in winter wheat line 'IDO835'

机译:冬小麦线“IDO835”识别和评估矮小的矮QTLS

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Dwarf bunt (DB), caused by Tilletia controversa J.G. Kuhn, and common bunt (CB), caused by T. caries and T. foetida, are two destructive diseases that reduce grain yield and quality in wheat. Breeding for bunt-resistant cultivars is important in many wheat production areas, especially where organic wheat is grown. However, few molecular markers have been used in selection of bunt resistance. In the present study, a doubled haploid (DH) population derived from the bunt-resistant line 'IDO835' and the susceptible cultivar 'Moreland' was evaluated for DB resistance in a field nursery in Logan, Utah, for four growing seasons. The population was genotyped with the Illumina 90 K SNP iSelect marker platform. Two major QTLs were consistently identified on chromosomes 6DL (Q.DB.ui-6DL) and 7AL (Q.DB.ui-7AL), explaining up to 53% and 38% of the phenotypic variation, respectively. Comparative study suggested that Q.DB.ui-6DL was located in the same region as the CB resistance gene Bt9, and Q.DB.ui-7AL was located at a novel locus for bunt resistance. Based on Chinese Spring reference sequence and annotations (IWGSC RefSeq v1.1), both resistance QTLs were mapped to disease resistance gene-rich (NBS-LRR and kinase genes) regions. To validate the identified QTL and design user-friendly markers for MAS, five SNPs were converted to Kompetitive Allele-Specific PCR (KASP) markers and used to genotype two validation panels, including a DH population and a diverse winter wheat population from USDA-ARS National Small Grain Collection, as well as a Bt gene investigation panel, consisting of 15 bunt differential lines and 11 resistant lines.
机译:矮人Bunt(DB),由Tiltetia争议造成J.G.由T.龋齿和T.Foetida引起的Kuhn和Common Bunt(CB)是两种破坏性疾病,减少了小麦的粮食产量和质量。 Bunt抗性品种的繁殖在许多小麦生产区域中都很重要,特别是在种植有机小麦的地方。然而,很少有分子标记用于选择间禁抗性。在本研究中,评估了来自抗性线“IDO835”和易感品种“莫尔兰”的双倍单倍体(DH)群体在犹他州Logan,犹他州洛根,庭院的DB抗性中评估了四个生长季节。用Illumina 90 K SNP Iselect标记平台进行基因分型。在染色体6dL(Q.db.ui-6dl)和7al(q.db.ui-7al)上一致地识别出两种主要QTL,分别解释了最高可达53%和38%的表型变异。对比研究表明,Q.db.ui-6dl位于与Cb电阻基因Bt9的相同区域中,Q.db.ui-7位位于一个用于抗性的新基因座。基于中国春季参考序列和注释(IWGSC Refseq V1.1),将抗性QTL均为致病基因富含(NBS-LRR和激酶基因)区域。为了验证所识别的QTL和设计MAS的用户友好标记,将五个SNP转化为基因类别特异性PCR(KASP)标记,并用于基因型两种验证面板,包括来自USDA-ARS的DH人口和多样的冬小麦人群国家小粮食集合,以及BT基因调查面板,包括15条差分线和11条抗性线。

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