首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Chromosomal location of the crown rust resistance gene Pc98 in cultivated oat (Avena sativa L.)
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Chromosomal location of the crown rust resistance gene Pc98 in cultivated oat (Avena sativa L.)

机译:栽培燕麦冠锈病基因PC98的染色体位置(Avena Sativa L.)

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Key message SNP loci linked to the crown rust resistance gene Pc98 were identified by linkage analysis and KASP assays were developed for marker-assisted selection in breeding programs. Crown rust is among the most damaging diseases of oat and is caused by Puccinia coronata var. avenae f. sp. avenae (Urban and Markova) (Pca). Host resistance is the preferred method to prevent crown rust epidemics. Pc98 is a race-specific, seedling crown rust resistance gene obtained from the wild oat Avena sterilis accession CAV 1979 that is effective at all growth stages of oat. Virulence to Pc98 has been very low in the Pca populations that have been tested. The objectives of this study were to develop SNP markers linked to Pc98 for use in marker-assisted selection and to locate Pc98 on the oat consensus map. The Pc98 gene was mapped using F-2:3 populations developed from the crosses Pc98/Bingo and Pc98/Kasztan, where Pc98 is a single-gene line carrying Pc98. Both populations were evaluated in seedling inoculation experiments. Pc98 was mapped relative to Kompetitive Allele-Specific PCR SNP markers in both populations, placing Pc98 on the Mrg20 linkage group of the consensus map. Pc98 was bracketed by two SNP markers GMI_ES22_c3052_382_kom399 and GMI_ES14_lrc18344_662_kom398 in the Pc98/Bingo mapping population with genetic distances of 0.9 cM and 0.3 cM, respectively. Pc98 co-segregated with four SNP markers in the Pc98/Kasztan population, and the closest flanking markers were GMI_DS_LB_6017_kom367 and avgbs2_153634.1.59_kom410 with genetic distances of 0.7 cM and 0.3 cM, respectively. Two SNP loci defined a haplotype that accurately predicted Pc98 status in a diverse group of oat germplasm, which will be valuable for marker-assisted selection of Pc98 in breeding of new oat cultivars.
机译:通过连杆分析鉴定链接到冠锈蚀基因PC98的关键消息SNP基因座,并开发了KASP测定以用于育种计划中的标记辅助选择。皇冠生锈是燕麦最损害的疾病之一,是由普昔锡冠状病症引起的。 Avenae F. SP。 Avenae(城市和马尔科瓦)(PCA)。宿主阻力是防止皇冠生锈流行病的首选方法。 PC98是一种种族特异性幼苗冠冠锈蚀基因,从野外燕麦艾滋病灭菌器加入型Cav 1979,在燕麦的所有生长阶段都有效。 PC98的毒力在已经测试的PCA种群中非常低。本研究的目标是开发与PC98相关联的SNP标记,以用于标记辅助选择,并在OAT共识地图上找到PC98。使用F-2:3种群体映射PC98基因:3个从交叉口PC98 / Bingo和PC98 / Kasztan开发的人群,其中PC98是携带PC98的单基因线。在幼苗接种实验中评估了两种群体。 PC98相对于Kompetitive等位基因特异性PCR SNP标记映射到两种群体中,将PC98放置在共识图的MRG20联系组上。 PC98被两个SNP标记GMI_ES22_C3052_382_KOM399和GMI_E14_LRC18344_662_KOM398分别在PC98 / Bingo映射群中的遗传距离分别为0.9厘米和0.3厘米。 PC98在PC98 / Kasztan群中使用四个SNP标记进行共聚,最接近的侧翼标记为GMI_DS_LB_6017_KOM367和AVGBS2_153634.1.59_KOM410分别为0.7厘米和0.3厘米。两个SNP基因座定义了一种单倍型,可准确地预测多种OAT种质中的PC98状态,这对于在繁殖新燕麦品种中的PC98中的标记辅助选择是有价值的。

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