Sram Jakub, Sommer Steve S, Liu Qiang
Department of Molecular Genetics, City of Hope National Medical Center, Duarte, CA 91010, USA.
Anal Biochem. 2008 Mar 1;374(1):41-7. doi: 10.1016/j.ab.2007.10.044. Epub 2007 Nov 4.
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.
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。