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Accurate Measurement of the Relative Abundance of Different DNA Species in Complex DNA Mixtures

机译:精确测量复杂DNA混合物中不同DNA物种的相对丰度

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摘要

A molecular tool that can compare the abundances of different DNA sequences is necessary for comparing intergenic or interspecific gene expression. We devised and verified such a tool using a quantitative competitive polymerase chain reaction approach. For this approach, we adapted a competitor array, an artificially made plasmid DNA in which all the competitor templates for the target DNAs are arranged with a defined ratio, and melting analysis for allele quantitation for accurate quantitation of the fractional ratios of competitively amplified DNAs. Assays on two sets of DNA mixtures with explicitly known compositional structures of the test sequences were performed. The resultant average relative errors of 0.059 and 0.021 emphasize the highly accurate nature of this method. Furthermore, the method's capability of obtaining biological data is demonstrated by the fact that it can illustrate the tissue-specific quantitative expression signatures of the three housekeeping genes G6pdx, Ubc, and Rps27 by using the forms of the relative abundances of their transcripts, and the differential preferences of Igf2 enhancers for each of the multiple Igf2 promoters for the transcription.
机译:可以比较不同DNA序列丰度的分子工具对于比较基因间或种间基因表达是必需的。我们使用定量竞争性聚合酶链反应方法设计并验证了这种工具。对于这种方法,我们采用了竞争者阵列,人工制造的质粒DNA(其中目标DNA的所有竞争者模板均以规定的比例排列),以及用于等位基因定量的解链分析以准确定量竞争性扩增DNA的分数比例。对两组具有明确已知测试序列组成结构的DNA混合物进行测定。所得的平均相对误差为0.059和0.021,强调了此方法的高度准确性。此外,该方法获得生物学数据的能力通过以下事实得以证明:该方法可以通过使用其转录本的相对丰度形式来说明三个管家基因G6pdx,Ubc和Rps27的组织特异性定量表达特征。 Igf2增强子对转录的多个Igf2启动子的不同偏爱。

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