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通过在寡核苷酸微阵列上进行直接多重聚合酶链反应扩增来获取基因组DNA中的单核苷酸多态性。

Accessing single nucleotide polymorphisms in genomic DNA by direct multiplex polymerase chain reaction amplification on oligonucleotide microarrays.

作者信息

Huber Martin, Mündlein Axel, Dornstauder Eva, Schneeberger Christian, Tempfer Clemens B, Mueller Manfred W, Schmidt Wolfgang M

机构信息

VBC-GENOMICS Bioscience Research GmbH, Rennweg 95b/5, A-1030 Vienna, Austria.

出版信息

Anal Biochem. 2002 Apr 1;303(1):25-33. doi: 10.1006/abio.2001.5565.

Abstract

This study introduces a DNA microarray-based genotyping system for accessing single nucleotide polymorphisms (SNPs) directly from a genomic DNA sample. The described one-step approach combines multiplex amplification and allele-specific solid-phase PCR into an on-chip reaction platform. The multiplex amplification of genomic DNA and the genotyping reaction are both performed directly on the microarray in a single reaction. Oligonucleotides that interrogate single nucleotide positions within multiple genomic regions of interest are covalently tethered to a glass chip, allowing quick analysis of reaction products by fluorescence scanning. Due to a fourfold SNP detection approach employing simultaneous probing of sense and antisense strand information, genotypes can be automatically assigned and validated using a simple computer algorithm. We used the described procedure for parallel genotyping of 10 different polymorphisms in a single reaction and successfully analyzed more than 100 human DNA samples. More than 99% of genotype data were in agreement with data obtained in control experiments with allele-specific oligonucleotide hybridization and capillary sequencing. Our results suggest that this approach might constitute a powerful tool for the analysis of genetic variation.

摘要

本研究介绍了一种基于DNA微阵列的基因分型系统,可直接从基因组DNA样本中检测单核苷酸多态性(SNP)。所描述的一步法将多重扩增和等位基因特异性固相PCR整合到一个芯片反应平台中。基因组DNA的多重扩增和基因分型反应均在微阵列上直接通过单一反应进行。用于检测多个感兴趣基因组区域内单核苷酸位置的寡核苷酸共价连接到玻璃芯片上,通过荧光扫描可快速分析反应产物。由于采用了一种四重SNP检测方法,同时探测有义链和反义链信息,因此可以使用简单的计算机算法自动分配和验证基因型。我们使用所述方法在单一反应中对10种不同的多态性进行平行基因分型,并成功分析了100多个人类DNA样本。超过99%的基因型数据与等位基因特异性寡核苷酸杂交和毛细管测序对照实验中获得的数据一致。我们的结果表明,这种方法可能构成分析遗传变异的有力工具。

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