Gilles P N, Wu D J, Foster C B, Dillon P J, Chanock S J
Nanogen Inc., San Diego, CA 92121, USA.
Nat Biotechnol. 1999 Apr;17(4):365-70. doi: 10.1038/7921.
We have developed a rapid assay for single nucleotide polymorphism (SNP) detection that utilizes electronic circuitry on silicon microchips. The method was validated by the accurate discrimination of blinded DNA samples for the complex quadra-allelic SNP of mannose binding protein. The microchip directed the transport, concentration, and attachment of amplified patient DNA to selected electrodes (test sites) creating an array of DNA samples. Through control of the electric field, the microchip enabled accurate genetic identification of these samples using fluorescently labeled DNA reporter probes. The accuracy of this approach was established by internal controls of dual labeled reporters and by using mismatched sequences in addition to the wild-type and variant reporter sequences to validate the SNP-genotype. The ability to customize this assay for multiple genes has advantages over other existing approaches.
我们开发了一种利用硅微芯片上的电子电路进行单核苷酸多态性(SNP)检测的快速测定法。该方法通过对甘露糖结合蛋白复杂四等位基因SNP的盲法DNA样本进行准确鉴别而得到验证。微芯片引导扩增后的患者DNA转运、浓缩并附着到选定电极(测试位点),形成DNA样本阵列。通过控制电场,微芯片使用荧光标记的DNA报告探针能够对这些样本进行准确的基因鉴定。这种方法的准确性通过双标记报告基因的内部对照以及除野生型和变异报告基因序列外使用错配序列来验证SNP基因型得以确立。针对多个基因定制此测定法的能力相较于其他现有方法具有优势。