In-situ polymerase chain reaction. An overview of methods, applications and limitations of a new molecular technique.

P Komminoth, A A Long
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Abstract

The in-situ polymerase chain reaction (in-situ PCR) is a novel molecular technique that combines the extreme sensitivity of the PCR with the anatomical localization provided by in-situ hybridization. A number of groups have recently reported studies using in-situ PCR for the detection of specifically amplified single-copy nucleic acid sequences in single cell preparations or low copy DNA sequences in tissue sections. In this overview, we describe the principles of in-situ PCR, review the applications of this technique and discuss future aspects of in-situ PCR. We critically compare the different in-situ PCR protocols described in the literature. Emphasis is placed on the absolute requirement for controls to allow accurate interpretation of results and the possible problems and pitfalls of the in-situ PCR methods, including artefacts related to diffusion of PCR products and non-specific incorporation of labelled nucleotides into fragmented DNA undergoing repair. It is concluded that this technique will eventually play an important role in specialized diagnostic laboratories in the evaluation of viral diseases, haematological and other malignancies which have unique genetic markers.

原位聚合酶链反应。综述了一种新的分子技术的方法、应用和局限性。
原位聚合酶链反应(原位PCR)是一种新型的分子技术,它将PCR的高度敏感性与原位杂交提供的解剖定位相结合。一些研究小组最近报道了利用原位PCR检测单细胞制剂中特异性扩增的单拷贝核酸序列或组织切片中低拷贝DNA序列的研究。在这篇综述中,我们描述了原位PCR的原理,回顾了该技术的应用,并讨论了原位PCR的未来发展方向。我们批判性地比较了文献中描述的不同的原位PCR方案。重点放在控制的绝对要求上,以允许准确解释结果和原位PCR方法可能存在的问题和陷阱,包括与PCR产物扩散和标记核苷酸非特异性结合到片段DNA中进行修复相关的伪影。结论是,该技术最终将在具有独特遗传标记的病毒性疾病、血液病和其他恶性肿瘤的专业诊断实验室中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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