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Fluorescence-based DHPLC for allelic quantification by single-nucleotide primer extension.

机译:基于荧光的DHPLC通过单核苷酸引物延伸进行等位基因定量。

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摘要

We have investigated the possibility of determining quantitatively the alleles of binary DNA polymorphisms by single-nucleotide primer extension (SNuPE) and fluorescence-based DHPLC. Using a polymorphism of interest to our group, ROX-labeled dideoxy CTP (ROX-ddCTP) was incorporated at the 3' end of the primer annealed to the template adjacent to the polymorphic site. The primer extension product was then resolved from the unincorporated dye terminator by ion-pair reversed-phase liquid chromatography. The signal intensity of incorporated ROX-ddCTP correlated well over one order of magnitude with the relative amount of the C-allele present in the genomic DNA template. We conclude that SNuPE, when combined with fluorescence-based DHPLC, can accurately determine the relative molar proportion of one allele in total DNA.
机译:我们已经研究了通过单核苷酸引物延伸(SNuPE)和基于荧光的DHPLC定量确定二进制DNA多态性等位基因的可能性。使用我们小组感兴趣的多态性,将ROX标记的双脱氧CTP(ROX-ddCTP)掺入与与多态性位点相邻的模板退火的引物的3'端。然后通过离子对反相液相色谱法从未结合的染料终止剂中分离出引物延伸产物。掺入的ROX-ddCTP的信号强度在一个数量级上与基因组DNA模板中存在的C等位基因的相对量相关性很好。我们得出的结论是,SNuPE与基于荧光的DHPLC结合使用时,可以准确确定总DNA中一个等位基因的相对摩尔比例。

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