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首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >Molecular marker analyses of pistachio rootstocks by Simple Sequence Repeats and Sequence-Related Amplified Polymorphisms.
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Molecular marker analyses of pistachio rootstocks by Simple Sequence Repeats and Sequence-Related Amplified Polymorphisms.

机译:阿月浑子砧木的分子标记分析,通过简单的序列重复和与序列相关的扩增多态性进行。

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Simple Sequence Repeat (SSR) and Sequence-Related Amplified Polymorphism (SRAP) molecular marker systems were used to analyse four commercially important pistachio rootstocks: two species of Pistacia atlantica (cv. 'Standard Atlantica'), P. integerrima [Pistacia chinensis subsp. integerrima] (cv. 'Pioneer Gold') and two interspecific hybrids of the same, 'Pioneer Gold II' ('PGII') and 'University of California at Berkeley 1' ('UCB-1'). A total of 35 putative alleles were detected by 12 SSR primer pairs with an average of 2.9 alleles per locus. The number of putative alleles ranged from 2 to 5 in the pistachio rootstocks tested. The number of bands produced by the SRAP protocol was highly variable, ranging from 11 to 38, with an average of 25.2 per primer combination. Eight primer combinations resulted in 104 (51%) polymorphic markers in these samples. SSR and SRAP markers successfully identified all pistachio rootstocks tested from their unique fingerprints. Both SSR and SRAP molecular markers confirmed that the observed variation in 'UCB-1' rootstock is genetic. Thus, there will always be variation among 'UCB-1' hybrid seedling progeny due to the segregation of alleles when propagated by seed. We also found evidence of contaminating pollen other than from P. integerrima in some hybrid 'UCB-1' rootstock progeny produced by closed pollination. Only alleles from the cultivar 'Standard Atlantica' were observed in abnormal 'UCB-1' rootstock in the nursery. We found that the poor performance of the scion cv. 'Kerman' on 'UCB-1' rootstock was not due to 'UCB-1' rootstocks displaying abnormal behaviour in the nursery. We have successfully developed two efficient marker systems for genome analyses in pistachio, which can be used for identification and management in pistachio rootstock production.
机译:简单序列重复(SSR)和序列相关的扩增多态性(SRAP)分子标记系统用于分析四种商业上重要的开心果砧木:两种Pistacia atlantica(cv。'Standard Atlantica'),P. integerrima [Pistacia chinensis subsp。整数”(简称“先锋金”)和两个同种的杂种,“先锋金II”(“ PGII”)和“加州大学伯克利分校1”(“ UCB-1”)。通过12对SSR引物对共检测到35个推定的等位基因,每个位点平均2.9个等位基因。在测试的开心果砧木中推定的等位基因数量范围为2至5。 SRAP协议产生的条带数量变化很大,范围从11到38,每个引物组合平均25.2。八个引物组合在这些样品中产生了104个(51%)多态性标记。 SSR和SRAP标记通过其独特的指纹成功鉴定了所有经过测试的开心果砧木。 SSR和SRAP分子标记均证实“ UCB-1”砧木中观察到的变异是遗传的。因此,由于等位基因通过种子繁殖时的分离,“ UCB-1”杂种幼苗后代之间总会有变异。我们还发现在封闭授粉产生的某些杂种'UCB-1'砧木后代中,污染了花粉而不是整形花粉的证据。在苗圃中,仅在异常的“ UCB-1”砧木中观察到了来自“标准大西洋”品种的等位基因。我们发现接穗简历的表现不佳。 'UCB-1'砧木上的'Kerman'不是由于'UCB-1'砧木在苗圃中表现出异常行为。我们已经成功开发了两个有效的开心果基因组分析标记系统,可用于开心果砧木生产中的鉴定和管理。

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