首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >The development of a PCR-based marker linked to resistance to the blackcurrant gall mite (Cecidophyopsis ribis Acari: Eriophyidae)
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The development of a PCR-based marker linked to resistance to the blackcurrant gall mite (Cecidophyopsis ribis Acari: Eriophyidae)

机译:基于PCR的标记与黑加仑gall螨的抗性相关的开发(Cecidophyopsis ribis Acari:Eriophyidae)

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摘要

Gall mite (Cecidophyopsis ribis) is the most serious pest of blackcurrant (Ribes nigrum L.), causing the damaging condition known as 'big bud' and also transmitting blackcurrant reversion virus (BRV) within and between plantations. The identification of resistant germplasm is at present a time-consuming and expensive process, dependent on field infestation plots. Resistance based on gene Ce introgressed from gooseberry has been used in UK breeding programmes for blackcurrant. Using a bulked segregant analysis, 90 AFLP primer combinations were screened and a linkage map constructed around the resistance locus controlled by Ce. Sixteen of the primer combinations produced a fragment in the resistant bulked progeny and the gall mite-resistant parent, but not in the susceptible bulked progeny and parent; subsequent testing on individual progeny identified an AFLP fragment closely linked to gall mite resistance. This fragment, designated E41M88-280, was converted to a PCR-based marker based on sequence-specific primers, amplifying only in resistant individuals. Validation of this marker across a range of susceptible and resistant blackcurrant germplasm with different genetic backgrounds confirmed its reliability in the identification of mite-resistant germplasm containing gene Ce. The conversion of an AFLP fragment to a sequence-based PCR marker simplifies its application and therefore increases its utility for selection of mite-resistant germplasm in high-throughput breeding programmes for blackcurrant.
机译:m螨(Cecidophyopsis ribis)是黑加仑(Ribes nigrum L.)最严重的害虫,造成了被称为“大芽”的破坏状况,并在种植园内和种植园之间传播了黑加仑逆转病毒(BRV)。目前,抗药性种质的鉴定是一个耗时且昂贵的过程,具体取决于田间侵染地块。基于醋栗渗入基因Ce的抗性已在英国黑加仑育种计划中使用。使用大量分离剂分析,筛选了90种AFLP引物组合,并在Ce控制的抗性基因座周围构建了连锁图。十六种引物组合在抗性膨大子代和耐gall螨的亲本中产生一个片段,但在易感膨大后代和亲本中不产生片段。随后对个体后代的测试确定了与gall螨抗性紧密相关的AFLP片段。将该片段命名为E41M88-280,基于序列特异性引物转换为基于PCR的标记,仅在抗性个体中进行扩增。在具有不同遗传背景的一系列易感和抗性黑加仑种质中对该标志物的验证证实了其在鉴定含有基因Ce的抗螨抗性种质中的可靠性。 AFLP片段向基于序列的PCR标记的转化简化了其应用,因此提高了其在黑醋栗高通量育种程序中选择抗螨虫种质的效用。

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