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Identification of molecular markers linked to disease resistance genes and applied marker-assisted breeding in wheat.

机译:鉴定与抗病基因相关的分子标记,并在小麦中应用标记辅助育种。

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摘要

Selection for resistance to the fungal pathogens Mycosphaerella graminicola and Stagonospora nodorum has effectively improved the performance of wheat cultivars against these pathogens. However, the gene-for-gene nature of resistance to M. graminicola and quantitative resistance to S. nodorum necessitates the need for testing their potential durability and mapping these genes in the wheat genome. This research was conducted to identify and map quantitative trait loci (QTL) for S. nodorum resistance and to use the mapped M. graminicola resistance gene Stb2 and the previously identified S. nodorum resistance QTL Qsng.sfr-3BS to build a stably inherited linkage block in the 3BS region. Two QTL for resistance to SNB in glumes were identified in a recombinant-inbred (RI) population from the cross of the Purdue University winter wheat breeding lines P91193D1 and P92201D5: Qsng.pur-2DL.1 was inherited from P91193D1 and Qsng.pur-2DL.2 from P92201D5. Qsng.pur-2DL.1 accounted for 12.3% of the phenotypic variation for resistance in southern Indiana, and 38.1% at South Perth, Australia; Qsng.pur-2DL.2 accounted for 6.9% and 11.2% of the phenotypic variation, respectively in southern Indiana and South Perth, Australia. The RI population and parent lines were phenotyped for S. nodorum glume resistance under field conditions in F8:10 at Evansville, Vincennes, and Lafayette, Indiana, USA in 2003; in F7:9 at South Perth, Australia in 2004; and F8:10 in greenhouse grown inoculation tests at Lafayette in 2003 and 2004. In the second research project, a linkage block between Stb2 and Qsng.sfr-3Bs was developed by crossing the STB resistant line DH115 (which derived its resistance from the cultivar Veranopolis) and the SNB resistant cultivar Arina. Over five-hundred F 2 plants were screened with M. graminicola and S. nodorum in the greenhouse at West Lafayette, IN in 2005. Several lines of this population were advanced for further testing and marker analysis. The phenotype of the 03739RB1-89-3 family was consistently STB and SNB resistant. Additionally, 164 F4:5 lines from this family were genotyped with the marker Xgwm389 and both marker alleles from each parent were amplified in all 164 lines supporting the phenotypic observations that indicate a linkage block between Stb2 and Qsng.sfr-3Bs has been developed.
机译:对真菌病原体Mycosphaerella graminicola和No. Stagonospora nodorum的抗性选择有效地提高了小麦品种对这些病原体的抗性。但是,由于对禾本科分枝杆菌的抗性具有基因对基因的特性,并且对No. S. nodorum的定量抗性需要测试其潜在的持久性并在小麦基因组中定位这些基因。进行了这项研究以鉴定和定位No. S. nodorum抗性的数量性状基因座(QTL),并使用定位的gra.graminicola抗性基因Stb2和先前鉴定的S. nodorum抗性QTL Qsng.sfr-3BS构建稳定的遗传连锁3BS区域中的块。在普渡大学(Purdue University)冬小麦育种系P91193D1和P92201D5的杂交后代中,鉴定了两个对颖花中SNB抗性的QTL:Qsng.pur-2DL.1源自P91193D1和Qsng.pur-来自P92201D5的2DL.2。 Qsng.pur-2DL.1占印第安纳州南部耐药性表型变异的12.3%,澳大利亚南珀斯地区为38.1%;在印第安纳州南部和澳大利亚南珀斯,Qsng.pur-2DL.2分别占表型变异的6.9%和11.2%。在野外条件下,于2003年在美国印第安纳州埃文斯维尔和印第安纳州拉斐特进行F8:10野外条件下,对RI种群和亲本表型进行了No. S. nodorum颖花抗性的表型分析。 2004年在澳大利亚南珀斯举行的F7:9比赛中;和2003年和2004年在拉斐特进行的温室种植接种试验中,F8:10和F8:10。在第二个研究项目中,通过跨越STB抗性系DH115(其对品种的抗性而得出),开发了Stb2和Qsng.sfr-3Bs之间的连接区。 Veranopolis)和SNB抗性品种Arina。 2005年,在印第安纳州西拉法叶的温室中,用禾本科分枝杆菌和诺氏链霉菌筛选了超过五百株F 2植物。对该种群的几系进行了进一步的测试和标记分析。 03739RB1-89-3家族的表型始终具有STB和SNB抗性。另外,用标记物Xgwm389对来自该家族的164个F4:5品系进行基因分型,并且在支持表型观察的所有164个品系中扩增了来自每个亲本的两个标记等位基因,这表明已开发出Stb2和Qsng.sfr-3Bs之间的连锁。

著录项

  • 作者

    Uphaus, James J.;

  • 作者单位

    Purdue University.;

  • 授予单位 Purdue University.;
  • 学科 Agriculture Agronomy.;Agriculture Plant Pathology.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 98 p.
  • 总页数 98
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:39:44

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