Isolation of Pikps, an allele of Pik, from the aus rice cultivar Shoni.

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Genes & genetic systems Pub Date : 2023-02-22 DOI:10.1266/ggs.22-00002
Basavaraj Kovi, Toshiyuki Sakai, Akira Abe, Eiko Kanzaki, Ryohei Terauchi, Motoki Shimizu
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引用次数: 0

Abstract

Blast disease caused by the filamentous fungus Pyricularia oryzae (syn. Magnaporthe oryzae) is one of the most destructive diseases of rice (Oryza sativa L.) around the globe. An aus cultivar, Shoni, showed resistance against at least four Japanese P. oryzae isolates. To understand Shoni's resistance against the P. oryzae isolate Naga69-150, genetic analysis was carried out using recombinant inbred lines developed by a cross between Shoni and the japonica cultivar Hitomebore, which is susceptible to Naga69-150. The result indicated that the resistance was controlled by a single locus, which was named Pi-Shoni. A QTL analysis identified Pi-Shoni as being located in the telomeric region of chromosome 11. A candidate gene approach in the region indicated that Pi-Shoni corresponds to the previously cloned Pik locus, and we named this allele Pikps. Loss of gene function mediated by RNA interference demonstrated that a head-to-head-orientated pair of NBS-LRR receptor genes (Pikps-1 and Pikps-2) are required for the Pikps-mediated resistance. Amino acid sequence comparison showed that Pikps-1 is 99% identical to Pikp-1, while Pikps-2 is identical to Pikp-2. Pikps-1 had one amino acid substitution (Pro351Ser) in the NBS domain as compared to Pikp-1. The recognition specificity of Pikps against known AVR-Pik alleles is identical to that of Pikp.

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稻瘟病等位基因Pikps的分离。
稻瘟病是由丝状真菌稻瘟病(pyricaria oryzae)引起的,是全球水稻(Oryza sativa L.)最具破坏性的病害之一。一个澳大利亚栽培品种Shoni对至少4个日本稻瘟病菌分离株显示出抗性。为了解小苗对稻瘟病菌Naga69-150的抗性,利用小苗与对Naga69-150敏感的粳稻品种Hitomebore杂交而成的重组自交系进行遗传分析。结果表明,该抗性由一个单位点控制,命名为Pi-Shoni。QTL分析鉴定Pi-Shoni位于11号染色体端粒区。该区域的候选基因方法表明,Pi-Shoni与先前克隆的Pik位点相对应,我们将该等位基因命名为Pikps。RNA干扰介导的基因功能丧失表明,一对头对头取向的NBS-LRR受体基因(Pikps-1和Pikps-2)是pikps介导的抗性所必需的。氨基酸序列比较表明,Pikps-1与Pikps-1的同源性为99%,Pikps-2与Pikps-2的同源性为99%。与Pikp-1相比,Pikp-1在NBS结构域有一个氨基酸取代(Pro351Ser)。Pikps对已知AVR-Pik等位基因的识别特异性与Pikp相同。
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来源期刊
Genes & genetic systems
Genes & genetic systems 生物-生化与分子生物学
CiteScore
1.50
自引率
0.00%
发文量
22
审稿时长
>12 weeks
期刊介绍: Genes & Genetic Systems , formerly the Japanese Journal of Genetics , is published bimonthly by the Genetics Society of Japan.
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