挑战所提出的PCR平台期的原因

Q1 Biochemistry, Genetics and Molecular Biology
Linda Jansson , Johannes Hedman
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引用次数: 22

摘要

尽管在各种生命科学应用中广泛使用聚合酶链反应(PCR),但在后期周期中扩增子产生受阻的原因尚未得到确定。这个所谓的平台期归因于引物或核苷酸的耗损或热分解,DNA聚合酶的热失活,以及引物退火和产物再杂交之间的竞争导致的产物积累,以及双链扩增子阻断DNA聚合酶。在目前的研究中,我们通过实验研究了PCR产物形成的限制因素。通过应用稳健且经过验证的qPCR分析,我们阐明了在反应中添加非目标扩增子和目标扩增子的影响,模拟了PCR周期后期的大量产物。此外,还探讨了引物浓度增加和试剂热稳定性的影响。我们的研究结果表明,大量的非靶扩增子通过与DNA聚合酶结合来抑制扩增,但这种效应可以通过添加更多的DNA聚合酶或延长退火/延伸时间来抵消。在反应中加入大量的靶扩增子作为模板,对扩增的抑制作用要小得多,尽管可以看到扩增率的降低。当引物浓度增加时,扩增率和最终产物产量都升高。综上所述,我们的结果表明,PCR平台形成的主要原因是引物耗尽,而不是产物积累或试剂降解。我们强调,由引物耗尽引起的PCR平台依赖于分析,即依赖于引物设计和引物特征,如引物-二聚体形成的概率。我们的发现有助于更好地理解控制PCR后期周期动力学的主要参数和持续产物形成的局限性,从而最终促进PCR优化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Challenging the proposed causes of the PCR plateau phase

Challenging the proposed causes of the PCR plateau phase

Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applications, the causes of arrested amplicon generation in late cycles have not been confidently identified. This so-called plateau phase has been attributed to depletion or thermal break-down of primers or nucleotides, thermal inactivation of the DNA polymerase, and product accumulation resulting in competition between primer annealing and product re-hybridization as well as blocking of DNA polymerase by double-stranded amplicons. In the current study, we experimentally investigate the proposed limiting factors of PCR product formation. By applying robust and validated qPCR assays, we elucidate the impact of adding non-target and target amplicons to the reactions, mimicking the high amount of products in late PCR cycles. Further, the impact of increased primer concentrations and thermal stability of reagents are explored. Our results show that high amounts of non-target amplicons inhibit amplification by binding to the DNA polymerase, but that this effect is counteracted by addition of more DNA polymerase or prolonged annealing/extension times. Adding high amounts of target amplicons that also act as templates in the reaction is far less inhibitory to amplification, although a decrease in amplification rate is seen. When primer concentrations are increased, both amplification rates and end-product yields are elevated. Taken together, our results suggest that the main cause of PCR plateau formation is primer depletion and not product accumulation or degradation of reagents. We stress that a PCR plateau caused by primer depletion is assay-dependent, i.e. dependent on the primer design and primer characteristics such as the probability of primer-dimer formation. Our findings contribute to an improved understanding of the major parameters controlling the PCR dynamics at later cycles and the limitations of continued product formation, which in the end can facilitate PCR optimization.

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来源期刊
Biomolecular Detection and Quantification
Biomolecular Detection and Quantification Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
14.20
自引率
0.00%
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审稿时长
8 weeks
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