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首页> 外文期刊>Acta Horticulturae >A RAPD marker linked to the resistance gene to Alternaria leaf spot ( Alternaria mali Roberts) in 'Qinguan' apple.
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A RAPD marker linked to the resistance gene to Alternaria leaf spot ( Alternaria mali Roberts) in 'Qinguan' apple.

机译:RAPD标记与“青冠”苹果中对链格孢菌叶斑病抗性基因( Alternaria mali Roberts)的链接。

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摘要

Resistance to Alternaria leaf spot in an F1 population of the cross of 'Qinguan' x 'Fuji' and its reciprocal cross 'Fuji' x 'Qinguan' was determined under natural conditions in 2006 and 2007. Among the progenies of both crosses, the SI values revealed some genetic features of quantitative traits demonstrating a continuous bi-modal distribution. This indicates that Alternaria leaf spot resistance in these two crosses may be controlled by a major gene in combination with some minor genes. Forty resistant, thirty-one susceptible progenies of the cross 'Qinguan' x 'Fuji' and 325 RAPD primers were chosen to detect markers linked to resistance based on the Bulked Segregant Analysis (BSA). A fragment, S428-854, present in 'Qinguan' and the resistant DNA pool, and absent in 'Fuji' and the susceptible DNA pool was obtained from the amplification by the primer S428. The distribution of S428-854 marker in F1 individuals showed that the molecular data of 56 individuals (78.9%) were consistent with the field resistance phenotype data. The S428-854 RAPD marker was sequenced and found to be 854 bp in length. Results of BLAST searches with this sequence in the NCBI database indicated that its homology to known sequences was no more than 30%. Structure analysis using DNASTAR software showed that this sequence did not have an open read frame, meaning that it does not have a complete gene structure. We have submitted this sequence to NCBI GeneBank as accession EU710766.
机译:在2006年和2007年的自然条件下,确定了'Qinguan'x'Fuji'的杂交F 1 种群及其倒数'Fuji'x'Qinguan'的F 1 种群对交链孢菌叶斑的抗性。在两个杂交的后代中,SI值揭示了数量性状的一些遗传特征,表明其具有连续的双峰分布。这表明这两个杂交中的交链孢菌叶斑病抗性可以由主要基因与一些次要基因结合控制。基于散粒分离分析(BSA),选择了四十个抗性,交叉“ Qinguan” x“ Fuji”和31个RAPD引物的31个易感子代,以检测与抗性相关的标记。通过引物S428的扩增,获得了“ Qinguan”和抗性DNA库中存在的,而“ Fuji”和易感DNA库中不存在的片段S428-854。 S428-854标记在F 1 个体中的分布表明56个个体的分子数据(78.9%)与田间抗性表型数据一致。对S428-854 RAPD标记进行测序,发现其长度为854 bp。在NCBI数据库中对该序列进行BLAST搜索的结果表明,该序列与已知序列的同源性不超过30%。使用DNASTAR软件进行的结构分析表明,该序列没有开放的阅读框,这意味着它没有完整的基因结构。我们已将该序列作为登录号EU710766提交给NCBI GeneBank。

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