首页> 美国卫生研究院文献>Breeding Science >Genetic basis of multiple resistance to the brown planthopper (Nilaparvata lugens Stål) and the green rice leafhopper (Nephotettix cincticeps Uhler) in the rice cultivar ‘ASD7’ (Oryza sativa L. ssp. indica)
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Genetic basis of multiple resistance to the brown planthopper (Nilaparvata lugens Stål) and the green rice leafhopper (Nephotettix cincticeps Uhler) in the rice cultivar ‘ASD7’ (Oryza sativa L. ssp. indica)

机译:水稻ASD7(Oryza sativa L. ssp。indica)品种对褐飞虱(Nilaparvata lugensStål)和绿稻飞虱(Nephotettix cincticeps Uhler)的多重抗性的遗传基础

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摘要

The rice cultivar ASD7 (Oryza sativa L. ssp. indica) is resistant to the brown planthopper (BPH; Nilaparvata lugens Stål) and the green leafhopper (Nephotettix virescens Distant). Here, we analyzed multiple genetic resistance to BPH and the green rice leafhopper (GRH; Nephotettix cincticeps Uhler). Using two independent F2 populations derived from a cross between ASD7 and Taichung 65 (Oryza sativa ssp. japonica), we detected two QTLs (qBPH6 and qBPH12) for resistance to BPH and one QTL (qGRH5) for resistance to GRH. Linkage analysis in BC2F3 populations revealed that qBPH12 controlled resistance to BPH and co-segregated with SSR markers RM28466 and RM7376 in plants homozygous for the ASD7 allele at qBPH6. Plants homozygous for the ASD7 alleles at both QTLs showed a much faster antibiosis response to BPH than plants homozygous at only one of these QTLs. It revealed that epistatic interaction between qBPH6 and qBPH12 is the basis of resistance to BPH in ASD7. In addition, qGRH5 controlled resistance to GRH and co-segregated with SSR markers RM6082 and RM3381. qGRH5 is identical to GRH1. Thus, we clarified the genetic basis of multiple resistance of ASD7 to BPH and GRH.
机译:水稻品种ASD7(印度稻(Oryza sativa L. ssp。indica))对褐飞虱(BPH; Nilaparvata lugensStål)和绿飞虱(Nephotettix virescens Distant)具有抗性。在这里,我们分析了对BPH和绿色稻叶蝉(GRH; Nephotettix cincticeps Uhler)的多重遗传抗性。使用两个独立的F2种群,它们来自ASD7和台中65(Oryza sativa ssp。japonica)之间的杂交,我们检测到两个对BPH的QTL(qBPH6和qBPH12)和一个对GRH的QTL(qGRH5)。在BC2F3群体中的连锁分析显示,qBPH12控制了对BPH的抗性,并在qBPH6的ASD7等位基因纯合植物中与SSR标记RM28466和RM7376共分离。在两个QTL上均对ASD7等位基因纯合的植物显示出对BPH的抗微生物反应要比仅在这些QTL之一上纯合的植物快得多。结果表明,qBPH6和qBPH12之间的上位相互作用是ASD7中抗BPH的基础。另外,qGRH5控制了对GRH的抗性,并与SSR标记RM6082和RM3381共分离。 qGRH5与 GRH1 相同。因此,我们阐明了ASD7对BPH和GRH多重耐药的遗传基础。

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