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Tagging Blast Resistance Gene Pi 1 in Rice (Oryza sativa) Using Candidate Resistance Genes

机译:利用候选抗性基因标记稻瘟病抗性基因Pi 1

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An F_3 population derived from C101LAC/CO39 containing 90 lines was analyzed for blast resistance with 48 candidate genes developed from resistance gene analogs (RGA) and suppression subtractive library. Genetic analysis confirmed that blast resistance of the population was controlled by a single gene Pi 1. One of the candidate'genes, R10 was identified as associated with the blast resistance gene on the long arm of chromosome 11 and mapped using a DH population derived from Azucena/IR64. A pair of PCR based primers was designed based on the sequence of R10 for marker-aided selection of the blast resistance gene. The recombination frequency between Pi 1 and the marker was estimated as 1.28%. It suggested that strategy of employing candidate genes is useful for gene identification and mapping: A new RFLP marker and the corresponding PCR marker for tagging of Pi 1 were provided.
机译:分析了来自C101LAC / CO39的F_3群体,其中包含90个品系,具有从抗性基因类似物(RGA)和抑制消减文库开发的48个候选基因的抗瘟性。遗传分析证实,该种群的瘟病抗性受单个基因Pi 1的控制。候选基因之一R10被鉴定为与11号染色体长臂上的瘟病抗性基因相关,并使用从Azucena / IR64。基于R10的序列设计了一对基于PCR的引物,用于标记辅助选择的抗稻瘟病基因。 Pi 1和标记之间的重组频率估计为1.28%。这表明利用候选基因的策略可用于基因鉴定和作图:提供了新的RFLP标记和相应的用于标记Pi 1的PCR标记。

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