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首页> 外文期刊>Limnology and oceanography, methods >QTL-seq approach identified genomic regions and diagnostic markers for rust and late leaf spot resistance in groundnut (Arachis hypogaea L.)
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QTL-seq approach identified genomic regions and diagnostic markers for rust and late leaf spot resistance in groundnut (Arachis hypogaea L.)

机译:QTL-SEQ方法鉴定了基因生锈和晚叶斑抗性的基因组区域和诊断标志物(Arachis Hypogaea L.)

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摘要

Rust and late leaf spot (LLS) are the two major foliar fungal diseases in groundnut, and their co-occurrence leads to significant yield loss in addition to the deterioration of fodder quality. To identify candidate genomic regions controlling resistance to rust and LLS, whole-genome resequencing (WGRS)-based approach referred as 'QTL-seq' was deployed. A total of 231.67 Gb raw and 192.10 Gb of clean sequence data were generated through WGRS of resistant parent and the resistant and susceptible bulks for rust and LLS. Sequence analysis of bulks for rust and LLS with reference-guided resistant parent assembly identified 3136 single-nucleotide polymorphisms (SNPs) for rust and 66 SNPs for LLS with the read depth of >= 7 in the identified genomic region on pseudomolecule A03. Detailed analysis identified 30 nonsynonymous SNPs affecting 25 candidate genes for rust resistance, while 14 intronic and three synonymous SNPs affecting nine candidate genes for LLS resistance. Subsequently, allele-specific diagnostic markers were identified for three SNPs for rust resistance and one SNP for LLS resistance. Genotyping of one RIL population (TAG 24 x GPBD 4) with these four diagnostic markers revealed higher phenotypic variation for these two diseases. These results suggest usefulness of QTL-seq approach in precise and rapid identification of candidate genomic regions and development of diagnostic markers for breeding applications.
机译:生锈和晚期叶斑病(LLS)是地生中的两个主要叶面真菌疾病,除了饲料质量的恶化之外,它们的共同发生导致显着的产量损失。为了识别控制耐锈病和LLS抗性的候选基因组区域,将被展开为“QTL-SEQ”的基于全部基因组重置(WGRS)的方法。通过WGR的抗性父母和耐锈和LLS的耐药和易感块,共产生231.67 GB原料和192.10 GB的干净序列数据。探针和LLS的序列分析与基准导向耐药父母组件鉴定了3136个单核苷酸多态性(SNP),用于鉴定在假调子A03上所鉴定的基因组区域中的读取深度> = 7的L10。详细分析确定了影响25个候选基因的30个非型SNP,用于抗抗锈病,而14个内肠道和三个同义SNP,影响九个候选基因的LLS抗性。随后,鉴定了等位基因特异性诊断标记,用于三个SNP,用于抗锈蚀,一个SNP用于LLS电阻。具有这四种诊断标记的一个RIL群体(标签24 x GPBD 4)的基因分型显示出这两种疾病的更高表型变异。这些结果表明QTL-SEQ方法在精确快速地鉴定候选基因组区域以及育种应用诊断标志物的发展。

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