Vaarno Jonne, Ylikoski Emmi, Meltola Niko J, Soini Juhani T, Hänninen Pekka, Lahesmaa Riitta, Soini Aleksi E
Laboratory of Biophysics, Institute of Biomedicine, University of Turku, Finland.
Nucleic Acids Res. 2004 Jul 19;32(13):e108. doi: 10.1093/nar/gnh102.
A new separation-free method for detection of single nucleotide polymorphisms (SNPs) is described. The method is based on the single base extension principle, fluorescently labeled dideoxy nucleotides and two-photon fluorescence excitation technology, known as ArcDia trade mark TPX technology. In this assay technique, template-directed single base extension is carried out for primers which have been immobilized on polymer microparticles. Depending on the sequence of the template DNA, the primers are extended either with a labeled or with a non-labeled nucleotide. The genotype of the sample is determined on the basis of two-photon excited fluorescence of individual microparticles. The effect of various assay condition parameters on the performance of the assay method is studied. The performance of the new assay method is demonstrated by genotyping the SNPs of human individuals using double-stranded PCR amplicons as samples. The results show that the new SNP assay method provides sensitivity and reliability comparable to the state-of-the-art SNaPshot trade mark assay method. Applicability of the new method in routine laboratory use is discussed with respect to alternative assay techniques.
本文描述了一种用于检测单核苷酸多态性(SNP)的新型免分离方法。该方法基于单碱基延伸原理、荧光标记的双脱氧核苷酸和双光子荧光激发技术,即ArcDia商标的TPX技术。在这种检测技术中,对固定在聚合物微粒上的引物进行模板导向的单碱基延伸。根据模板DNA的序列,引物用标记或未标记的核苷酸进行延伸。基于单个微粒的双光子激发荧光来确定样品的基因型。研究了各种检测条件参数对检测方法性能的影响。通过使用双链PCR扩增子作为样本对人类个体的SNP进行基因分型,证明了新检测方法的性能。结果表明,新的SNP检测方法提供了与最先进的SNaPshot商标检测方法相当的灵敏度和可靠性。针对替代检测技术,讨论了该新方法在常规实验室使用中的适用性。