PCR伪影对天然聚丙烯酰胺凝胶电泳微卫星位点分型效率的影响。

TSitologiia i genetika Pub Date : 2016-05-01
R A Kulibaba, Y V Liashenko
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引用次数: 0

摘要

研究了不同分子遗传标记(Indel和SSR)在扩增反应中不同类型伪产物的形成。结果表明,杂合样品在扩增过程中会形成DNA杂双体,作为靶基因和微卫星位点的片段。对微卫星基因座纯合扩增产物进行天然聚丙烯酰胺凝胶电泳,发现了不属于异双工DNA的特异性附加片段。据推测,额外的片段属于一种特殊类型的同工双链DNA -非线性同工双链。分析表明,非线性同双工DNA的形成发生在PCR的20-25个周期,无论是在单个样品的扩增,还是从凝胶中剪切出的单个DNA片段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of the PCR artifacts on the genotyping efficiency by the microsatellite loci using native polyacrylamide gel electrophoresis.

The formation of different types of the artifacts in the amplification reaction with using different classes of the molecular-genetic markers (Indel and SSR) was studied. It was shown that DNA heteroduplexes formed during amplification of heterozygous samples, as fragments of target genes and microsatellite loci. During the electrophoresis in native polyacrylamide gel of the amplification products of homozygous samples for microsatellite loci it was revealed specific additional fragments that do not belong to the class of heteroduplex DNA. It was supposed, that the additional fragments belong to a special type of homoduplex DNA – non-linear homoduplexes. The analysis revealed that the formation of a non-linear homoduplex DNA takes place on the 20–25 cycle of the PCR, both at the amplification of the individual samples, and individual DNA fragments that was cut out from the gel.

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