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QTLs underlying the genetic interrelationship between efficient compatibility of Bradyrhizobium strains with soybean and genistein secretion by soybean roots

机译:根瘤菌菌株与大豆的有效相容性与大豆根中染料木黄酮分泌之间的遗传相互关系的QTL

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摘要

Soybean plants establish symbiotic relationships with soil rhizobia which form nodules on the plant roots. Nodule formation starts when the plant roots exudate isoflavonoids that induce nod gene expression of a specific Bradyrhizobium. We examined the specific indigenous rhizobia that form nodules with the soybean cultivars Peking and Tamahomare in different soils. PCR-RFLP analysis targeted to the 16S-23S rRNA gene internal transcribed spacer (ITS) region of the bacterial type of each root nodule showed that Bradyrhizobium japonicum (USDA110-type) and Bradyrhizobium elkanii (USDA94-type) had high compatibility with the Tamahomare and Peking cultivars, respectively. We grew 93 recombinant inbred lines (RIL) of soybean seeds derived from the cross between Peking and Tamahomare in three different field soils and identified the indigenous rhizobia nodulating each line using the same PCR-RFLP analysis. QTL analysis identified one QTL region in chromosome-18 with a highly significant additive effect that controls compatibility with both B. japonicum USDA110 and B. elkanii USDA94. We also measured the amount of daidzein and genistein secretion from roots of the 93 RILs by HPLC analysis. QTL analysis showed one QTL region in chromosome-18 controlling genistein secretion from roots and coinciding with that regulating compatibility of specific indigenous rhizobia with soybean. The amount of genistein may be a major regulatory factor in soybean-rhizobium compatibility.
机译:大豆植物与土壤根瘤菌建立了共生关系,根瘤菌在植物根部形成根瘤。当植物根系分泌异黄酮类物质时,结节开始形成,异黄酮诱导特定的缓生根瘤菌的nod基因表达。我们研究了在不同土壤中与北京和大豆栽培种的结节形成根瘤的特定土著根瘤菌。针对每个根结节细菌类型的16S-23S rRNA基因内部转录间隔区(ITS)区域的PCR-RFLP分析表明,日本短枝根瘤菌(USDA110型)和埃尔卡氏根瘤菌(USDA94型)与Tamahomare具有高度相容性和北京品种。我们在三种不同的田间土壤中种植了93种源自北京和塔马霍马杂交的大豆种子重组近交系(RIL),并使用相同的PCR-RFLP分析鉴定了结节成根的原生根瘤菌。 QTL分析鉴定了在第18号染色体中的一个QTL区域,该区域具有高度显着的加性效应,该效应控制了与日本血吸虫USDA110和美国羽衣芽孢杆菌USDA94的相容性。我们还通过HPLC分析测量了93个RIL根中黄豆苷元和染料木黄酮的分泌量。 QTL分析显示,第18号染色体上的一个QTL区控制着染料木黄酮从根部的分泌,并与调节特定本地根瘤菌与大豆的相容性相吻合。金雀异黄素的数量可能是大豆-根瘤菌相容性的主要调节因素。

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