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首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Qualitative and quantitative trait loci conditioning resistance to Puccinia coronata pathotypes NQMG and LGCG in the oat (Avena sativa L.) cultivars Ogle and TAM O-301
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Qualitative and quantitative trait loci conditioning resistance to Puccinia coronata pathotypes NQMG and LGCG in the oat (Avena sativa L.) cultivars Ogle and TAM O-301

机译:燕麦(Avena sativa L.)品种Ogle和TAM O-301的定性和定量性状基因座条件适应对Puccinia coronata病态NQMG和LGCG的抗性

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摘要

Mapping disease resistance loci relies on the type and precision of phenotypic measurements. For crown rust of oat, disease severity is commonly assessed based on visual ratings of infection types (IT) and/or diseased leaf area (DLA) of infected plants in the greenhouse or field. These data can be affected by several variables including; (i) non-uniform disease development in the field; (ii) atypical symptom development in the greenhouse; (iii) the presence of multiple pathogenic races or pathotypes in the field, and (iv) rating bias. To overcome these limitations, we mapped crown rust resistance to single isolates in the Ogle/TAM O-301 (OT) recombinant inbred line (RIL) population using detailed measurements of IT, uredinia length (UL) and relative fungal DNA (FDNA) estimates determined by q-PCR. Measurements were taken on OT parents and recombinant inbred lines (RIL) inoculated with Puccinia coronata pathotypes NQMG and LGCG in separate greenhouse and field tests. Qualitative mapping identified an allele conferred by TAM O-301 on linkage group (LG) OT-11, which produced a bleached fleck phenotype to both NQMG and LGCG. Quantitative mapping identified two major quantitative trait loci (QTL) originating from TAM O-301 on LGs OT-11 and OT-32 which reduced UL and FDNA of both isolates in all experiments. Additionally, minor QTLs that reduced UL and FDNA were detected on LGs OT-15 and OT-8, originating from TAM O-301, and on LG OT-27, originating from Ogle. Detailed assessments of the OT population using two pathotypes in both the greenhouse and field provided comprehensive information to effectively map the genes responsible for crown rust resistance in Ogle and TAM O-301 to NQMG and LGCG.
机译:绘制抗病基因座图谱依赖于表型测量的类型和精度。对于燕麦冠锈病,通常根据温室或田地中被感染植物的感染类型(IT)和/或病叶面积(DLA)的目视等级评估疾病的严重程度。这些数据可能会受到以下几个变量的影响: (i)野外疾病的不均匀发展; (ii)温室中出现非典型症状; (iii)野外存在多种病原体或病原体,以及(iv)评级偏差。为了克服这些限制,我们使用对IT,尿素长度(UL)和相对真菌DNA(FDNA)估计的详细测量,将Ogle / TAM O-301(OT)重组自交系(RIL)群体中的单个分离株的冠锈病抗性进行了映射通过q-PCR测定。在单独的温室和田间试验中,对OT亲本和接种了Puccinia coronata病原体NQMG和LGCG的重组自交系(RIL)进行了测量。定性作图鉴定了由TAM O-301赋予的连锁群(LG)OT-11等位基因,该等位基因对NQMG和LGCG产生了漂白的斑点表型。定量作图鉴定了两个主要的定量性状基因座(QTL),它们来自LG OT-11和OT-32上的TAM O-301,在所有实验中均降低了两个分离株的UL和FDNA。此外,在源自TAM O-301的LG OT-15和OT-8以及源自Ogle的LG OT-27上检测到了降低UL和FDNA的次要QTL。使用温室和田间两种病态型对OT种群进行的详细评估提供了全面的信息,可以有效地将负责Ogle和TAM O-301的冠锈病抗性基因定位到NQMG和LGCG。

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