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Phytophthora Root Rot Resistance in Soybean E00003

机译:大豆E00003的疫霉根腐病抗性

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Phytophthora root rot (PRR) is a devastating disease in soybean [Glycine max (L.) Merr.] production. Michigan elite soybean E00003 is resistant to Phytophthora sojae and has been used as a resistance source in breeding. Genetic control of PRR resistance in this source is unknown. To facilitate marker-assisted selection (MAS), the PRR resistance loci in E00003 and their map locations need to be determined. In this study, a genetic mapping approach was used to identify major PRR-resistant loci in E00003. The mapping population consists of 240 F4a€“derived lines developed by crossing E00003 with the P. sojae susceptible line PI 567543C. In 2009 and 2010, the mapping population was evaluated in the greenhouse for PRR resistance against P. sojae races 1, 4, and 7, using modified rice (Oryza sativa L.) grain inoculation method. The population was genotyped with seven simple sequence repeat (SSR) and three single nucleotide polymorphism (SNP) markers derived from bulk segregant analysis. The heritability of resistance in the population ranged from 83 to 94%. A major locus, contributing 50 to 76% of the phenotypic variation, was mapped within a 3 cM interval in the Rps1 region. The interval was further saturated with more BARCSOY SSRs and SNPs with TaqMan assays. Two SSRs and three SNPs within the Rps1k gene were highly associated with PRR resistance in the mapping population. The major resistance gene in E00003 is either allelic or tightly linked to Rps1k.The molecular markers located in the Rps1k gene can be used to improve MAS for PRR resistance.
机译:疫霉根腐病(PRR)是大豆[Glycine max(L.)Merr。]生产中的毁灭性疾病。密歇根州优质大豆E00003对大豆疫霉菌有抗性,并已被用作育种的抗性来源。此来源中PRR抗性的遗传控制尚不清楚。为了促进标记辅助选择(MAS),需要确定E00003中的PRR抗性基因座及其图谱位置。在这项研究中,使用遗传图谱方法来鉴定E00003中主要的PRR抗性基因座。测绘种群由240个F4a衍生品系组成,这些品系通过将E00003与大豆疫霉易感品系PI 567543C杂交而形成。在2009年和2010年,使用改良稻谷(Oryza sativa L.)谷物接种方法,评估了温室中作图种群对大豆疫霉1、4和7的PRR抗性。该种群的基因分型采用了七个来自批量分离分析的简单重复序列(SSR)和三个单核苷酸多态性(SNP)标记。人群中抵抗力的遗传力范围为83%至94%。一个主要的基因座,占表型变异的50%至76%,被定位在Rps1区域的3 cM区间内。通过TaqMan分析,更多的BARCSOY SSR和SNP使该区间进一步饱和。 Rps1k基因中的两个SSR和三个SNP与绘图人群中的PRR抗性高度相关。 E00003中的主要抗性基因是等位基因或与Rps1k紧密连接。位于Rps1k基因中的分子标记可用于改善MAS对PRR的抗性。

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