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Development and characterization of SSR markers in Chinese cherry (Prunus pseudocerasus Lindl.).

机译:樱桃(Srunus pseudocerasus Lindl。)SSR标记的开发和鉴定。

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摘要

24 simple sequence repeat (SSR) markers were isolated and characterized in P. pseudocerasus Lindl. from the cultivar 'Laiyang Short cherry'. To amplify SSR loci primers were developed to flank each repeat region, and they were initially tested on 6 cherry samples using chemiluminescence detection. 18 loci where shown to be polymorphic and the number of alleles detected per locus varied from 2 to 6.12 loci were chosen for the analysis of 26 cultivars grown in North China using the semi-automatic system ABI PRISM 377. These 12 markers showed a high level of genetic polymorphism with a total of 75 alleles; the number of alleles ranged from 4 to 10 per locus, with an average level of 6.3. The mean expected and observed heterozygosity was 0.743 (range: 0.680-0.845) and 0.829 (range: 0.730-0.930) respectively. The estimated frequency of null alleles showed a positive value for 3 loci, but except for 1 locus, the values were very low. The total value for the probability of identity was 7.01x10-13. Paternity exclusion probability was very high (0.999), sufficiently high to study pollen flow.
机译:分离出24个简单的序列重复(SSR)标记,并在假单胞菌Lind1中表征。来自“莱阳矮樱桃”品种。为了扩增SSR基因座,开发了在每个重复区域侧翼的引物,并且最初使用化学发光检测法在6个樱桃样品上对其进行了测试。使用半自动系统ABI PRISM 377,选择了18个基因座,这些基因座显示为多态性,每个位点检测到的等位基因数量在2至6.12个基因座之间进行分析。分析了华北地区生长的26个品种。这12个标记物显示出高水平遗传多态性,共有75个等位基因;每个位点的等位基因数量范围为4至10,平均水平为6.3。平均预期和观察到的杂合度分别为0.743(范围:0.680-0.845)和0.829(范围:0.730-0.930)。无效等位基因的估计频率显示3个基因座为正值,但除了1个基因座外,这些值非常低。同一性概率的总值为7.01x10-13。亲子排斥的可能性非常高(0.999),足以研究花粉流动。

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