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首页> 外文期刊>Molecular genetics and genomics: MGG >Inheritance, fine-mapping, and candidate gene analyses of resistance to soybean mosaic virus strain SC5 in soybean
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Inheritance, fine-mapping, and candidate gene analyses of resistance to soybean mosaic virus strain SC5 in soybean

机译:大豆耐大豆病毒株SC5抗耐药性,精细映射和候选基因分析

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摘要

Soybean mosaic virus (SMV) is one of the most devastating pathogens for soybeans in China. Among the country-wide 22 strains, SC5 dominates in Huang-Huai and Changjiang valleys. For controlling its damage, the resistance gene was searched through Mendelian inheritance study, gene fine-mapping, and candidate gene analysis combined with qRT-PCR (quantitative real-time polymerase chain reaction) analysis. The parents F-1, F-2, and RILs (recombinant inbred lines) of the cross Kefeng-1 (Resistance, R) x NN1138-2 (Susceptible, S) were used to examine the inheritance of SC5-resistance. The F-1 was resistant and the F-2 and RILs segregated in a 3R:1S and 1R:1S ratio, respectively, indicating a single dominant gene conferring the Kefeng-1 resistance. Subsequently, the genomic region conferring the resistance was found in "Bin 352-Bin353 with 500 kb" on Chromosome 2 using the phenotyping data of the 427 RILs and a high-density genetic map with 4703 bin markers. In the 500 kb genomic region, 38 putative genes are contained. The association analysis between the SNPs in a putative gene and the resistance phenotype for the 427 RILs prioritized 11 candidate genes using Chi-square criterion. The expression levels of these genes were tested by qRT-PCR. On infection with SC5, 7 out of the 11 genes had differential expression in Kefeng-1 and NN1138-2. Furthermore, integrating SNP-phenotype association analysis with qRT-PCR expression profiling analysis, Glyma02g13495 was found the most possible candidate gene for SC5-resistance. This finding can facilitate the breeding for SC5-resistance through marker-assisted selection and provide a platform to gain a better understanding of SMV-resistance gene system in soybean.
机译:大豆马赛克病毒(SMV)是中国大豆最疣的病原体之一。在全国范围的22个菌株中,SC5在黄淮和长江山谷占主导地位。为了控制其损伤,通过孟德尔遗传研究,基因精细映射和候选基因分析与QRT-PCR(定量实时聚合酶链反应)分析相结合的抗性基因。父母F-1,F-2和RILS(重组近亲)的交叉Kefeng-1(抗性,R)X NN1138-2(易感,S)用于检查SC5抗性的遗传。 F-1分别是抗性的,并且分别在3R:1S和1R:1S的比例中分别抵抗抗性和RIL,表明赋予kefeng-1抗性的单一主要基因。随后,使用427个rils的表型数据和4703箱标记物的高密度遗传图谱,在染色体2上赋予抗抗性的基因组区域。在500kb基因组区域中,含有38个推定基因。使用Chi-Square标准,推定基因中SNP与427个候选基因的抗性表型之间的关联分析。通过QRT-PCR测试这些基因的表达水平。在11个基因中用SC5的感染有7种基因在Kefeng-1和NN1138-2中具有鉴别表达。此外,将SNP-表型关联分析与QRT-PCR表达分析分析相结合,发现Glyma02G13495是SC5抗性最可能的候选基因。这种发现可以通过标记辅助选择来促进SC5抗性的繁殖,并提供平台,以便在大豆中更好地了解SMV抗性基因体系。

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