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Restriction fragment length polymorphism analysis of host-plant resistance to four maize pathogens.

机译:宿主植物对四种玉米病原体抗性的限制性片段长度多态性分析。

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摘要

Restriction fragment length polymorphism (RFLP) markers were used to investigate host plant resistance to four maize pathogens in 117 maize recombinant inbred lines (RILS), derived from the cross of Hi31 (a B68 conversion) and Ki14 (a Thai inbred). The four pathogens are maize mosaic virus (MMV), Erwinia stewartii, Puccinia polysora, and Exserohilum turcicum. The phenotypic data of RILs were analyzed with 127 RFLP loci using MAPMAKER/QTL and single factor analysis of variance.;Ninety-one RILs were evaluated for MMV resistance in a disease nursery in Hawaii in the summer of 1994. Fifty RILs were classified as susceptible and forty-one as resistant. Loci on chromosome 3 near the centromere showed the largest effects, indicating that a major MMV resistance gene was located in this region. This gene, previously named mv, was mapped on chromosome 3, 4 cM and 5.6 cM from RFLP markers umc102 and php20508, respectively.;Seventy-one RILs and ten sub-lines of each parent were planted at Henderson, Kentucky for evaluation and were naturally infected by E. stewartii. Thirty-eight RILs were classified as resistant and thirty-three as susceptible. A major gene conferring resistance to E. stewartii, designated sw1, was mapped on the short arm of chromosome 1, 4 cM and 8.2 cM from RFLP markers umc167 and umc67, respectively.;One hundred and seventeen RILs and twenty sub-lines of each parent were planted at Waimanalo, Hawaii and one hundred and seven RILs were planted at Mindanao, The Philippines to evaluate P. polysora resistance under natural infection. Five QTLs were mapped on chromosomes 2, 4, 6, 9, and 10. The QTL on chromosome 6 appeared to play a particularly important role in conditioning race-nonspecific resistance to P. polysora.;One hundred and ten RILs and ten sub-lines of each parent were evaluated for race-nonspecific resistance to E. turcicum at Mealani, Hawaii in 1993. A clear 1:1 segregation for general resistance characterized RILs in this nursery. Ninety-five RILs were planted in two separate trials to evaluate the response to race 0 and race 1 of E. turcicum, respectively, at Urbana, Illinois in 1994. The QTL located on chromosomal region 3S was important in conferring the race-nonspecific resistance to E. turcicum.
机译:限制性片段长度多态性(RFLP)标记用于研究寄主植物对来自Hi31(B68转化)和Ki14(泰国近交)杂交的117种玉米重组自交系(RILS)中四种玉米病原体的抗性。四种病原体是玉米花叶病毒(MMV),斯氏欧文氏菌(Erwinia stewartii),多叶紫锥虫(Puccinia polysora)和Exserohilum turcicum。使用MAPMAKER / QTL和单因素方差分析,用127个RFLP位点分析了RIL的表型数据。1994年夏天,在夏威夷的一个疾病苗圃中,对91个RIL进行了MMV耐药性评估。将50个RIL归为易感性和四十一抗性。着丝粒附近第3号染色体上的基因座显示出最大的作用,表明主要的MMV抗性基因位于该区域。该基因以前命名为mv,分别通过RFLP标记umc102和php20508定位在3号染色体,4 cM和5.6 cM染色体上;在肯塔基州的亨德森种植了71个RIL和每个亲本的10个亚系进行评估,自然被埃氏杆菌感染。 38个RIL被归类为耐药,33个为易感。分别通过RFLP标记umc167和umc67在1号染色体的短臂,4 cM和8.2 cM的短臂上绘制了一个赋予对斯氏大肠杆菌的抗性的主要基因,分别为sw1和117个RIL和20个亚系亲本在夏威夷的威玛纳诺种植,一百零七个RIL种植在菲律宾的棉兰老岛,以评估自然感染下的多毛疟原虫抗性。五个QTL被定位在2、4、6、9和10号染色体上。6号染色体上的QTL在调节对多孢疟原虫的种族非特异性抗性中似乎起着特别重要的作用。110个RIL和10个亚种1993年在夏威夷的Mealani中评估了每对亲本的品系对斑节肠杆菌的非种族非特异性抗性。该育苗室中RIL的一般抗性清楚地1:1隔离。 1994年在两项单独的试验中种植了95个RIL,以分别评估伊利诺伊州厄巴纳市对斑节对虾0号和1号种族的反应。位于3S染色体区域的QTL在赋予非种族特异性抗性方面很重要到E. turcicum。

著录项

  • 作者

    Ming, Reiguang.;

  • 作者单位

    University of Hawai'i at Manoa.;

  • 授予单位 University of Hawai'i at Manoa.;
  • 学科 Agronomy.;Genetics.;Plant pathology.
  • 学位 Ph.D.
  • 年度 1995
  • 页码 152 p.
  • 总页数 152
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:49:37

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