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使用MAC-PR(微卫星DNA等位基因计数-峰比率)方法对多倍体中的等位基因构型进行分配。

Assignment of allelic configuration in polyploids using the MAC-PR (microsatellite DNA allele counting-peak ratios) method.

作者信息

Esselink G D, Nybom H, Vosman B

机构信息

Department of Biodiversity and Breeding, Plant Research International, P.O. Box 16, 6700 AA Wageningen, The Netherlands.

出版信息

Theor Appl Genet. 2004 Jul;109(2):402-8. doi: 10.1007/s00122-004-1645-5. Epub 2004 Apr 14.

Abstract

Polysomic inheritance frequently results in the simultaneous occurrence of several microsatellite DNA alleles on a single locus. The MAC-PR (microsatellite DNA allele counting-peak ratios) method was recently developed for the analysis of polyploid plants and makes use of the quantitative values for microsatellite allele peak areas. To date, this approach has only been used in plants with known genetic relationships. We report here the application of MAC-PR for the first time to random samples of unknown pedigrees. We analysed six microsatellite loci using a set of tetraploid ornamental rose ( Rosa x hybrida L.) varieties. For each locus, all alleles were analysed in pairwise combinations in order to determine their copy number in the individual samples. This was accomplished by calculating the ratios between the peak areas for two alleles in all of the samples where these two alleles occurred together. The allele peak ratios observed were plotted in a histogram, and those histograms that produced at least two well-separated groups were selected for further analysis. Mean allelic peak ratio values for these groups were compared to the relationships expected between alleles in hypothetical configurations of the locus investigated. Using this approach, we were able to assign precise allelic configurations (the actual genotype) to almost all of the varieties analysed for five of the six loci investigated. MAC-PR also appears to be a very effective tool for detecting 'null' alleles in polyploid species.

摘要

多体遗传常常导致在单个基因座上同时出现几个微卫星DNA等位基因。MAC-PR(微卫星DNA等位基因计数-峰值比率)方法是最近为分析多倍体植物而开发的,它利用了微卫星等位基因峰值面积的定量值。迄今为止,这种方法仅用于具有已知遗传关系的植物。我们在此首次报告MAC-PR在未知谱系随机样本中的应用。我们使用一组四倍体观赏玫瑰(Rosa x hybrida L.)品种分析了六个微卫星基因座。对于每个基因座,对所有等位基因进行成对组合分析,以确定它们在各个样本中的拷贝数。这是通过计算在所有同时出现这两个等位基因的样本中两个等位基因峰值面积之间的比率来完成的。将观察到的等位基因峰值比率绘制在直方图中,并选择那些产生至少两个明显分开的组的直方图进行进一步分析。将这些组的平均等位基因峰值比率值与所研究基因座的假设构型中等位基因之间预期的关系进行比较。使用这种方法,对于所研究的六个基因座中的五个,我们能够为几乎所有分析的品种确定精确的等位基因构型(实际基因型)。MAC-PR似乎也是检测多倍体物种中“无效”等位基因的非常有效的工具。

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