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Mapping of the apple powdery mildew resistance gene Pl1 and its genetic association with an NBS-LRR candidate resistance gene.

机译:苹果白粉病抗性基因Pl1的定位及其与NBS-LRR候选抗性基因的遗传关联。

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Molecular markers for the major apple powdery mildew resistance gene Pl1 were identified and are presently used in marker-assisted selection in apple breeding. However, the precise map position of the Pl1 gene in the apple genome was not known. The objectives of this investigation were the identification of the Malus linkage group (LG) carrying the Pl1 locus, mapping of the resistance gene by simple sequence repeat (SSR) markers, and the analysis of genetic associations between the Pl1 gene and the numerous NBS-LRR resistance gene candidates already mapped in the apple genome. A two-step linkage mapping was used, based on two different apple families. The identification of LG 12 carrying Pl1 was performed indirectly by mapping the SCAR marker AT20 in an apple progeny for which there was a core genetic map but no mildew data available. Then, the position of Pl1 on LG 12 was determined by SSR markers in a second population which has been scored for mildew over 6 years in a greenhouse and in the field. The SSR Hi07f01, previously mapped on LG 12 [Tree Genet. Genomes, 2 (2006), 202] cosegregated with AT20 and was closely linked (~1 cM) to the Pl1 gene. The TIR-NBS-LRR resistance gene analogue 15G11 mapped by the SSCP technique was also closely linked to the Pl1 resistance locus and might be a candidate for Pl1 itself, a second powdery mildew major resistance gene (Pld, [Theor. Appl. Genet., 110 (2004), 175]), or two scab resistance genes (Vg, [IOBC/WPRS Bull., 23 (2000), 245]; Vb, [Genome, 49 (2006), 1238]) which all seem to be located in a common R gene cluster at the distal end of apple LG 12.
机译:鉴定了主要的苹果白粉病抗性基因Pl1的分子标记,目前用于苹果育种中的标记辅助选择。但是,Pl1基因在苹果基因组中的精确定位图尚不清楚。这项研究的目的是鉴定携带Pl1基因座的Malus连锁基团(LG),通过简单序列重复(SSR)标记对抗性基因进行定位以及分析Pl1基因与众多NBS-之间的遗传关联。已经在苹果基因组中定位的LRR抗性基因候选物。基于两个不同的苹果家族,使用了两步链接映射。通过在苹果后代中绘制SCAR标记AT20的图谱来间接鉴定携带Pl1的LG 12,苹果后代具有核心的遗传图谱,但没有霉菌数据。然后,通过SSR标记在第二个种群中确定了Pl1在LG 12上的位置,该种群已在温室和田间进行了6年的防霉评分。 SSR Hi07f01,先前映射到LG 12 [Tree Genet。 Genomes,2(2006),202]与AT20共同分离,并与Pl1基因紧密相连(〜1 cM)。通过SSCP技术定位的TIR-NBS-LRR抗性基因类似物15G11也与Pl1抗性基因座密切相关,可能是第二个白粉病主要抗性基因Pl1本身的候选基因(Pld,[Theor.Appl.Genet。 ,110(2004),175])或两个or疮抗性基因(Vg,[IOBC / WPRS Bull。,23(2000),245]; Vb,[基因组,49(2006),1238]),似乎位于苹果LG 12远端的常见R基因簇中。

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