Ballantyne Kaye N, van Oorschot Roland A H, Muharam Iman, van Daal Angela, John Mitchell R
Biology Division, Victoria Police Forensic Services Department, Macleod, 3085 VIC, Australia.
Anal Biochem. 2007 Sep 15;368(2):222-9. doi: 10.1016/j.ab.2007.05.017. Epub 2007 May 24.
Although multiple displacement amplification (MDA) is being used increasingly to amplify genomes, the amplification bias generated by the varphi29 polymerase can be a concern with genotyping applications. It has been noted that the bias is pronounced with small template amounts, particularly with single nucleotide polymorphism (SNP) and short tandem repeat (STR) genotyping. Bias may occur between loci, or between alleles within a locus, and may differ between sample donors at the same loci. Previous research has suggested that omitting denaturation of the template prior to amplification can reduce the observed bias significantly. Comparison of the two methods (with and without denaturation) has found that nondenaturation of template reverses the direction of bias observed between allelic pairs following MDA. By combining two MDA reactions, one denatured and one nondenatured, the bias was found to be reduced significantly, aiding copy number analysis and subsequent genotyping.
尽管多重置换扩增(MDA)越来越多地用于扩增基因组,但φ29聚合酶产生的扩增偏差在基因分型应用中可能是一个问题。已经注意到,这种偏差在少量模板时尤为明显,特别是在单核苷酸多态性(SNP)和短串联重复序列(STR)基因分型中。偏差可能发生在不同位点之间,或同一位点的不同等位基因之间,并且在相同位点的样本供体之间可能有所不同。先前的研究表明,在扩增前省略模板的变性可以显著降低观察到的偏差。两种方法(有变性和无变性)的比较发现,模板的非变性会逆转MDA后等位基因对之间观察到的偏差方向。通过结合两个MDA反应,一个变性一个非变性,发现偏差显著降低,有助于拷贝数分析和后续基因分型。