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Genomic analysis of the rhg1 locus: candidate genes that underlie soybean resistance to the cyst nematode

机译:rhg1基因座的基因组分析:大豆对囊肿线虫抗性的候选基因

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The rhg1 gene or genes lie at a recessive or co-dominant locus, necessary for resistance to all Hg types of the soybean (Glycine max (L.) Merr.) cyst nematode (Heterodera glycines I.). The aim here was to identify nucleotide changes within a candidate gene found at the rhg1 locus that were capable of altering resistance to Hg types 0 (race 3). A 1.5 +/- 0.25 cM region of chromosome 18 (linkage group G) was shown to encompass rhg1 using recombination events from four near isogenic line populations and nine DNA markers. The DNA markers anchored two bacterial artificial chromosome (BAC) clones 21d9 and 73p6. A single receptor like kinase (RLK; leucine rich repeat-transmembrane-protein kinase) candidate resistance gene was amplified from both BACs using redundant primers. The DNA sequence showed nine alleles of the RLK at Rhg1 in the soybean germplasm. Markers designed to detect alleles showed perfect association between allele 1 and resistance to soybean cyst nematode Hg types 0 in three segregating populations, fifteen additional selected recombination events and twenty-two Plant Introductions. A quantitative trait nucleotide in the RLK at rhg1 was inferred that alters A47 to V47 in the context of H297 rather than N297. Contiguous DNA sequence of 315 kbp of chromosome 18 (about 2 cM) contained additional gene candidates that may modulate resistance to other Hg-types including a variant laccase, a hydrogen-sodium ion antiport and two proteins of unknown function. A molecular basis for recessive and co-dominant resistance that involves interactions among paralagous disease-resistance genes was inferred that would improve methods for developing new nematode-resistant soybean cultivars.
机译:rhg1基因或多个基因位于隐性或共显性位点,对于抵抗所有Hg类型的大豆(Glycine max(L.)Merr。)囊肿线虫(Heterodera glycines I.)具有抗性。此处的目的是鉴定在rhg1基因座处发现的候选基因中的核苷酸变化,该变化能够改变对Hg类型0(种族3)的抗性。使用来自四个近等基因系群体和九个DNA标记的重组事件,显示了18号染色体(连接群G)的1.5 +/- 0.25 cM区域包含rhg1。 DNA标记锚定了两个细菌人工染色体(BAC)克隆21d9和73p6。使用冗余引物从两个BAC扩增单个受体样激酶(RLK;富含亮氨酸的重复跨膜蛋白激酶)候选抗性基因。 DNA序列显示大豆种质中Rhg1的RLK的9个等位基因。旨在检测等位基因的标记在三个分离群体,另外十五个选定的重组事件和二十二个植物引种中显示了等位基因1与对0型大豆囊肿线虫Hg的抗性之间的完美关联。推断在rhg1的RLK中的定量性状核苷酸在H297而非N297的情况下将A47变为V47。 18号染色体315 kbp的连续DNA序列(约2 cM)包含其他基因候选物,这些候选物可能调节对其他Hg型的抗性,包括变体漆酶,氢-钠离子反转运蛋白和两种功能未知的蛋白。推测了一种隐性和共显性抗性的分子基础,该分子基础涉及寄生虫抗病基因之间的相互作用,这将改善开发新的抗线​​虫性大豆品种的方法。

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