首页> 外文期刊>Frontiers in Plant Science >Fine Mapping and Identification of a Novel Phytophthora Root Rot Resistance Locus RpsZS18 on Chromosome 2 in Soybean
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Fine Mapping and Identification of a Novel Phytophthora Root Rot Resistance Locus RpsZS18 on Chromosome 2 in Soybean

机译:大豆疫霉根腐病抗性基因 RpsZS18 在大豆2号染色体上的精细定位与鉴定

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Phytophthora root rot (PRR) caused by Phytophthora sojae is a major soybean disease that causes severe economic losses worldwide. Using soybean cultivars carrying a Rps resistance gene is the most effective strategy for controlling this disease. We previously detected a novel Phytophthora resistance gene, RpsZS18 , on chromosome 2 of the soybean cultivar Zaoshu18. The aim of the present study was to identify and finely map RpsZS18 . We used 232 F_(2:3)families generated from a cross between Zaoshu18 (resistant) and Williams (susceptible) as the mapping population. Simple sequence repeat (SSR) markers distributed on chromosome 2 were used to map RpsZS18 . First, 12 SSR markers linked with RpsZS18 were identified by linkage analyses, including two newly developed SSR markers, ZCSSR33 and ZCSSR46, that flanked the gene at distances of 0.9 and 0.5 cM, respectively. Second, PCR-based InDel markers were developed based on sequence differences between the two parents and used to further narrow down the mapping region of RpsZS18 to 71.3 kb. Third, haplotype analyses were carried out in the RpsZS18 region using 14 soybean genotypes with whole-genome resequencing. We detected six genes with unique haplotype sequences in Zaoshu18. Finally, quantitative real-time PCR assays of the six genes revealed an EF-hand calcium-binding domain containing protein encoding gene ( Glyma.02g245700 ), a pfkB carbohydrate kinase encoding gene ( Glyma.02g245800 ), and a gene with no functional annotation ( Glyma.02g246300 ), are putative candidate PRR resistance genes. This study provides useful information for breeding P. sojae -resistant soybean cultivars.
机译:大豆疫霉引起的疫霉根腐病(PRR)是一种主要的大豆疾病,在世界范围内造成严重的经济损失。使用携带Rps抗性基因的大豆品种是控制该病的最有效策略。我们之前在大豆品种Zaoshu18的2号染色体上检测到了新的疫霉抗性基因RpsZS18。本研究的目的是鉴定和精细映射RpsZS18。我们使用了Zaoshu18(抗性)和Williams(易感)之间的杂交产生的232个F_(2:3)族作为作图种群。简单的重复序列(SSR)标记分布在2号染色体上,用于定位RpsZS18。首先,通过连锁分析鉴定了与RpsZS18连锁的12个SSR标记,包括两个新开发的SSR标记ZCSSR33和ZCSSR46,它们分别位于基因的0.9和0.5 cM处。第二,基于PCR的InDel标记是基于两个亲本之间的序列差异而开发的,并用于将RpsZS18的定位区域进一步缩小至71.3 kb。第三,在RpsZS18区使用14个大豆基因型进行了全基因组重测序,进行了单倍型分析。我们在Zaoshu18中检测到六个具有独特单倍型序列的基因。最后,对这六个基因进行实时定量PCR分析,发现一个含有EF手钙结合结构域的蛋白编码基因(Glyma.02g245700),一个pfkB碳水化合物激酶编码基因(Glyma.02g245800)和一个没有功能注释的基因(Glyma.02g246300)是推定的候选PRR抗性基因。这项研究为育种抗大豆疫霉的大豆品种提供了有用的信息。

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