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使用3'封闭引物的基于微阵列的DNA重测序

Microarray-based DNA resequencing using 3' blocked primers.

作者信息

Sram Jakub, Sommer Steve S, Liu Qiang

机构信息

Department of Molecular Genetics, City of Hope National Medical Center, Duarte, CA 91010, USA.

出版信息

Anal Biochem. 2008 Mar 1;374(1):41-7. doi: 10.1016/j.ab.2007.10.044. Epub 2007 Nov 4.

Abstract

To exceed the throughput and accuracy of conventional sequencing technologies, we tested a method (pyrophosphorolysis-activated polymerization [PAP]) of nucleic acid amplification that uses 3' blocked primers (Ps). As proof-of-principle, we resequenced a 20-bp region of the factor IX gene with a microarray of Ps. Ps discriminate 3' end mismatches with ultra-high specificity as well as mismatches along their lengths with high specificity. We correctly identified two wild-type samples as well as all mismatches, including three single-base substitutions, one microdeletion, one microinsertion, and one heterozygous mutation. Despite limitations in the primer purity, the signal/noise ratio between the matched and mismatched Ps sometimes exceeded 1000. Thus, PAP resequencing shows great potential for accurate and high-throughput microarray-based resequencing.

摘要

为了超越传统测序技术的通量和准确性,我们测试了一种核酸扩增方法(焦磷酸解激活聚合反应 [PAP]),该方法使用3' 封闭引物(Ps)。作为原理验证,我们使用Ps微阵列对凝血因子IX基因的一个20 bp区域进行了重测序。Ps对3' 末端错配具有超高特异性,对其长度上的错配也具有高特异性。我们正确鉴定了两个野生型样本以及所有错配情况,包括三个单碱基替换、一个微缺失、一个微插入和一个杂合突变。尽管引物纯度存在局限性,但匹配和错配Ps之间的信噪比有时超过1000。因此,PAP重测序在基于微阵列的准确且高通量重测序方面显示出巨大潜力。

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