Lovmar Lovisa, Fredriksson Mona, Liljedahl Ulrika, Sigurdsson Snaevar, Syvänen Ann-Christine
Molecular Medicine, Department of Medical Sciences, Entrance 70, 3rd Floor, Research Department 2, Uppsala University Hospital, SE-75185 Uppsala, Sweden.
Nucleic Acids Res. 2003 Nov 1;31(21):e129. doi: 10.1093/nar/gng129.
Whole genome amplification (WGA) procedures such as primer extension preamplification (PEP) or multiple displacement amplification (MDA) have the potential to provide an unlimited source of DNA for large-scale genetic studies. We have performed a quantitative evaluation of PEP and MDA for genotyping single nucleotide polymorphisms (SNPs) using multiplex, four-color fluorescent minisequencing in a microarray format. Forty-five SNPs were genotyped and the WGA methods were evaluated with respect to genotyping success, signal-to-noise ratios, power of genotype discrimination, yield and imbalanced amplification of alleles in the MDA product. Both PEP and MDA products provided genotyping results with a high concordance to genomic DNA. For PEP products the power of genotype discrimination was lower than for MDA due to a 2-fold lower signal-to-noise ratio. MDA products were indistinguishable from genomic DNA in all aspects studied. To obtain faithful representation of the SNP alleles at least 0.3 ng DNA should be used per MDA reaction. We conclude that the use of WGA, and MDA in particular, is a highly promising procedure for producing DNA in sufficient amounts even for genome wide SNP mapping studies.
全基因组扩增(WGA)程序,如引物延伸预扩增(PEP)或多重置换扩增(MDA),有潜力为大规模基因研究提供无限的DNA来源。我们使用微阵列形式的多重四色荧光微测序对PEP和MDA进行了单核苷酸多态性(SNP)基因分型的定量评估。对45个SNP进行了基因分型,并从基因分型成功率、信噪比、基因型判别能力、产量以及MDA产物中等位基因的不平衡扩增等方面对WGA方法进行了评估。PEP和MDA产物的基因分型结果与基因组DNA高度一致。由于信噪比低2倍,PEP产物的基因型判别能力低于MDA。在所有研究方面,MDA产物与基因组DNA无法区分。每个MDA反应至少应使用0.3 ng DNA,以获得SNP等位基因的准确代表。我们得出结论,使用WGA,特别是MDA,即使对于全基因组SNP图谱研究,也是一种极有前景的大量生产DNA的方法。