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Detection and fine mapping of two quantitative trait loci for partial resistance to stripe virus in rice (Oryza sativa L.)

机译:水稻对条带病毒部分抗性的两个数量性状基因座的检测和精细定位

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摘要

Rice stripe virus (RSV) is one of the most destructive pathogens of rice (Oryza sativa L.) in East Asia. Development of resistant varieties offers a more economical and efficient way to control this disease. In the present study, tests using four inoculation methods were used on 85 backcross inbred lines of Sasanishiki (japonica)/Habataki (indica) to map quantitative trait loci (QTL) conferring resistance to RSV. One QTL on chromosome 3 and two on chromosome 11 were detected, jointly explaining 18–47 % of the trait variance. The QTL (qSTV11 HAB -1 and qSTV11 HAB -2) on chromosome 11 were closely linked, and mapped in the intervals G257-RM457 and RM457-RM187, respectively. The stabilities of qSTV11 HAB -1 and qSTV11 HAB -2 were validated using a set of 38 established chromosome segmental substitution lines. The two QTL, when combined, showed higher resistance than either of them alone in both field and mass inoculation tests, indicating additivity. Fine mapping of the two genes was carried out using 147 recombined F2:3 lines selected from 2,750 secondary F2 plants of the cross Sasanishiki/SL437. Four SSR (simple sequence repeat) and eight InDel (insertion–deletion) markers newly developed to fine-map the two loci. According to the Nipponbare genomic sequence, qSTV11 HAB -1 was localized to a 333.2-kb interval which was about 230 kb from the well-known Stvb-i. The other locus, qSTV11 HAB -2, which appears to be a new QTL for RSV resistance, was delimited to a 203.9-kb region. Four flanking markers (R15, RM209, R69 and R73) can be used in marker-assisted selection. These results provide an opportunity for map-based cloning of qSTV11 HAB -1 and qSTV11 HAB -2, thereby promoting the breeding program of RSV resistance.
机译:水稻条纹病毒(RSV)是东亚地区最具破坏性的水稻病原体之一。抗性品种的开发为控制该病提供了更经济和有效的途径。在本研究中,使用了四种接种方法的测试在Sasanishiki(日本)/ Habataki(印度)的85个回交自交系上进行绘制,以绘制出赋予RSV抗性的定量性状位点(QTL)。在3号染色体上检测到一个QTL,在11号染色体上检测到两个QTL,共同解释了18–47%的性状变异。第11号染色体上的QTL(qSTV11 HAB -1和qSTV11 HAB -2)紧密相连,并分别映射在间隔G257-RM457和RM457-RM187中。 qSTV11 HAB -1和qSTV11 HAB -2的稳定性已使用一组38条已建立的染色体片段替代系进行了验证。在田间和大规模接种测试中,两个QTL结合使用时显示出比单独使用任何一个更高的抗性,表明具有可加性。使用选自Sasanishiki / SL437杂交的2,750株次生F2植物的147个重组F2:3系对这两个基因进行了精细定位。新开发了四个SSR(简单序列重复)和八个InDel(插入-删除)标记,以精确定位两个基因座。根据日本晴基因组序列,qSTV11 HAB -1被定位在一个333.2-kb的间隔,距著名的Stvb-i约230 kb。另一个基因座qSTV11 HAB -2(似乎是RSV抗性的新QTL)被划定为203.9kb区域。四个侧翼标记(R15,RM209,R69和R73)可用于标记辅助选择。这些结果为qSTV11 HAB -1和qSTV11 HAB -2的基于图谱的克隆提供了机会,从而促进了RSV抗性的育种程序。

著录项

  • 来源
    《Molecular Breeding》 |2012年第3期|p.1379-1391|共13页
  • 作者单位

    State Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Provincial Center of Plant Gene Engineering, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China;

    State Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Provincial Center of Plant Gene Engineering, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China;

    State Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Provincial Center of Plant Gene Engineering, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China;

    State Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Provincial Center of Plant Gene Engineering, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China;

    State Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Provincial Center of Plant Gene Engineering, Nanjing Agricultural University,;

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  • 正文语种 eng
  • 中图分类
  • 关键词

    Rice stripe virus; QTL analysis; Fine mapping; Oryza sativa L.; Partial resistance;

    机译:水稻条纹病毒;QTL分析;精细定位;水稻(Oryza sativa L.);部分抗性;

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