首页> 外文期刊>Acta Agriculturae Slovenica >Interlaboratory comparison of fig (Ficus carica L.) microsatellite genotyping data and determination of reference alleles
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Interlaboratory comparison of fig (Ficus carica L.) microsatellite genotyping data and determination of reference alleles

机译:无花果(无花果)微卫星基因分型数据的实验室间比较和参考等位基因的确定

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Microsatellites have been identified as the marker of choice in plant genotyping projects. However, due to length discrepancies obtained between different laboratories for the same allele, interlaboratory comparison of fingerprinting results is often a difficult task. The objectives of this study were to compare genotyping results of two laboratories, to evaluate genetic parameters of microsatellite markers and to determine reference allele sizes for fig cultivars from the Istrian peninsula. Genotyping results of ninety fig ( Ficus carica L.) accessions were comparable between the laboratories despite differences observed when comparing electropherograms of different capillary electrophoresis systems. Differences in lengths of the same alleles were detected due to different PCR methods and laboratory equipment, but the distances between alleles of the same locus were preserved. However, locus FSYC01 exhibited one allele dropout which led to misidentification of 28 heterozygotes as homozygote individuals suggesting this locus as unreliable. Allele dropout was assigned to the tail PCR technology or to a touchdown PCR protocol. Genotypes of twenty-four reference cultivars from the Istrian peninsula were confirmed by both laboratories. These results will contribute to the usage of markers with greater reliability, discrimination power and consequently, to more reliable standardization with other fig genotyping projects.
机译:微卫星已被确定为植物基因分型计划中的选择标记。但是,由于不同实验室之间对于同一等位基因的长度差异,指纹结果的实验​​室间比较通常是一项艰巨的任务。这项研究的目的是比较两个实验室的基因分型结果,评估微卫星标记的遗传参数,并确定伊斯特拉半岛无花果品种的参考等位基因大小。尽管比较不同毛细管电泳系统的电泳图时观察到差异,但在实验室之间有90种无花果(Ficus carica L.)品种的基因分型结果可比。由于PCR方法和实验室设备的不同,检测到的等位基因的长度存在差异,但保留了相同基因座的等位基因之间的距离。但是,基因座FSYC01表现出一个等位基因缺失,导致28个杂合子被误认为是纯合子个体,提示该基因座不可靠。等位基因缺失被分配给尾部PCR技术或着陆PCR方案。两个实验室都证实了来自伊斯特拉半岛的二十四个参考品种的基因型。这些结果将有助于使用具有更高可靠性,辨别力的标记,并因此有助于与其他无花果基因分型项目更可靠的标准化。

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