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采用探针捕获与改良等位基因特异性引物延伸反应(MASPER)相结合的高通量单碱基错配检测法对 UDP-葡糖醛酸基转移酶 1A1(UGT1A1)进行基因分型。

High-throughput single-base mismatch detection for genotyping of UDP-glucuronosyltransferase (UGT1A1) with probe capture assay coupled with modified allele-specific primer extension reaction (MASPER).

机构信息

Japan Clinical Laboratories, Kumiyama, Kuze-gun, Kyoto, Japan.

出版信息

J Clin Lab Anal. 2010;24(2):85-91. doi: 10.1002/jcla.20359.

Abstract

We have developed a new method based on specific primer extension reactions coupled with plate hybridization for high-throughput genotyping of single-base mutations. To improve the switching characteristics of the primer extension reaction, we introduced an artificial mismatch two bases upstream of the 3'-terminal base in the detection primers. A set of primers that correspond to wild-type and mutant DNA segments can be used to accurately analyze single-base mutations. The termini of these primers are at the mutation positions. The primer extension products produced by polymerase chain reaction (PCR) were captured by an oligonucleotide probe immobilized on the surface of microtiter wells and were detected by a colorimetric assay using the streptavidin-conjugated horseradish peroxidase. We used the new method to genotype 96 individuals for 211G>A (G71R) and 119 for 1456T>G (Y486D) in the UDP-glucuronosyltransferase1A1 gene; the results were completely concordant with those found by direct sequencing. The proposed method includes ordinary PCR and a microplate assay format, and may be used in routine laboratory tests.

摘要

我们开发了一种新的方法,基于特定引物延伸反应与平板杂交相结合,用于高通量单碱基突变的基因分型。为了改善引物延伸反应的切换特性,我们在检测引物的 3'-末端碱基上游引入了一个人工错配碱基对。一组与野生型和突变型 DNA 片段相对应的引物可用于准确分析单碱基突变。这些引物的末端位于突变位置。聚合酶链反应 (PCR) 产生的引物延伸产物被固定在微孔板表面的寡核苷酸探针捕获,并通过辣根过氧化物酶标记的链亲和素进行比色测定进行检测。我们使用新方法对 96 个人的 UDP-葡萄糖醛酸基转移酶 1A1 基因中的 211G>A (G71R) 和 119 个 1456T>G (Y486D) 进行了基因分型;结果与直接测序完全一致。所提出的方法包括普通 PCR 和微孔板检测方法,可用于常规实验室检测。

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