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首页> 外文期刊>Theoretical and Applied Genetics >Identification and mapping of AFLP markers linked to peanut (Arachis hypogaea L.) resistance to the aphid vector of groundnut rosette disease
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Identification and mapping of AFLP markers linked to peanut (Arachis hypogaea L.) resistance to the aphid vector of groundnut rosette disease

机译:与花生(花生)蚜虫媒介抗性相关的AFLP标记的鉴定和作图

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摘要

Groundnut rosette disease is the most destructive viral disease of peanut in Africa and can cause serious yield losses under favourable conditions. The development of disease-resistant cultivars is the most effective control strategy. Resistance to the aphid vector, Aphis craccivora, was identified in the breeding line ICG 12991 and is controlled by a single recessive gene. Bulked segregant analysis (BSA) and amplified fragment length polymorphism (AFLP) analysis were employed to identify DNA markers linked to aphid resistance and for the development of a partial genetic linkage map. A F2:3 population was developed from a cross using the aphid-resistant parent ICG 12991. Genotyping was carried out in the F2 generation and phenotyping in the F3 generation. Results were used to assign individual F2 lines as homozygous-resistant, homozygous-susceptible or segregating. A total of 308 AFLP (20 EcoRI+3/MseI+3, 144 MluI+3/MseI+3 and 144 PstI+3/MseI+3) primer combinations were used to identify markers associated with aphid resistance in the F2:3 population. Twenty putative markers were identified, of which 12 mapped to five linkage groups covering a map distance of 139.4 cM. A single recessive gene was mapped on linkage group 1, 3.9 cM from a marker originating from the susceptible parent, that explained 76.1% of the phenotypic variation for aphid resistance. This study represents the first report on the identification of molecular markers closely linked to aphid resistance to groundnut rosette disease and the construction of the first partial genetic linkage map for cultivated peanut.
机译:花生花环病是非洲花生中最具破坏性的病毒性疾病,在有利条件下会导致严重的单产下降。抗病品种的发展是最有效的控制策略。在繁殖系ICG 12991中鉴定了对蚜虫载体Aphis craccivora的抗性,并由单个隐性基因控制。使用散装分离子分析(BSA)和扩增片段长度多态性(AFLP)分析来鉴定与蚜虫抗性相关的DNA标记,并开发部分遗传连锁图谱。使用抗蚜虫亲本ICG 12991从杂交中培育出F2:3 种群。在F2 世代进行基因分型,在F3 世代进行表型分型。结果用于将单个F2 品系指定为纯合抗性,纯合易感性或分离。总共308个AFLP(20个EcoRI + 3 / MseI + 3、144个MluI + 3 / MseI + 3和144个PstI + 3 / MseI + 3)引物组合用于鉴定与F2:3 < / sub>人口。鉴定了20个推定标记,其中12个定位到五个连锁组,覆盖139.4 cM的定位距离。一个单一的隐性基因被定位在连锁群1上,从易感亲本起源的一个标记3.9 cM定位,这解释了76.1%的蚜虫抗性表型变异。这项研究代表了有关鉴定与蚜虫对花生玫瑰花叶病抗性紧密相关的分子标记的首次报道,并首次建立了栽培花生的部分遗传连锁图谱。

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  • 来源
    《Theoretical and Applied Genetics》 |2004年第7期|1426-1433|共8页
  • 作者单位

    Agricultural Research Council-Grain Crops InstituteDepartment of Plant Sciences University of the Free State;

    Natural Resources Institute University of Greenwich at MedwayDepartment of Agricultural Sciences Imperial College London;

    Natural Resources Institute University of Greenwich at MedwayNR International;

    UMR 1096 CIRAD-Biotrop;

    Chitedze Agricultural Research Station ICRISAT-MalawiAgricultural Research Council-Grain Crops Institute;

    Natural Resources Institute University of Greenwich at Medway;

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