Stevens Aaron J, Taylor Millie G, Pearce Frederick Grant, Kennedy Martin A
Department of Pathology, University of Otago, Christchurch 8140, New Zealand.
Biomolecular Interaction Centre, School of Biological Sciences, University of Canterbury, Christchurch 8140, New Zealand.
G3 (Bethesda). 2017 Mar 10;7(3):1019-1025. doi: 10.1534/g3.116.038687.
Loss of one allele during polymerase chain reaction (PCR) amplification of DNA, known as allelic dropout, can be caused by a variety of mechanisms. Allelic dropout during PCR may have profound implications for molecular diagnostic and research procedures that depend on PCR and assume biallelic amplification has occurred. Complete allelic dropout due to the combined effects of cytosine methylation and G-quadruplex formation was previously described for a differentially methylated region of the human imprinted gene, We now demonstrate that this parent-of-origin specific allelic dropout can potentially occur at several other genomic regions that display genomic imprinting and have propensity for G-quadruplex formation, including , , , , , and These findings demonstrate that systematic allelic dropout during PCR is a general phenomenon for regions of the genome where differential allelic methylation and G-quadruplex motifs coincide, and suggest that great care must be taken to ensure biallelic amplification is occurring in such situations.
在DNA的聚合酶链反应(PCR)扩增过程中一个等位基因的丢失,即所谓的等位基因脱扣,可能由多种机制引起。PCR过程中的等位基因脱扣可能对依赖PCR且假定发生双等位基因扩增的分子诊断和研究程序产生深远影响。先前已描述了由于胞嘧啶甲基化和G-四链体形成的综合作用导致的完全等位基因脱扣,涉及人类印记基因的一个差异甲基化区域。我们现在证明,这种亲本来源特异性等位基因脱扣可能潜在地发生在其他几个显示基因组印记且有形成G-四链体倾向的基因组区域,包括……这些发现表明,PCR过程中的系统性等位基因脱扣是基因组中差异等位基因甲基化和G-四链体基序重合区域的普遍现象,并表明在这种情况下必须格外小心以确保发生双等位基因扩增。