Komminoth P, Long A A
Department of Pathology, University of Zürich, Switzerland.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(2):67-73.
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(in-situ PCR)是一种新型分子技术,它将PCR的极高灵敏度与原位杂交提供的解剖定位相结合。最近有多个研究小组报道了使用原位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。在本综述中,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。我们对文献中描述的不同原位PCR方案进行了严格比较。重点强调了对照对于准确解读结果的绝对必要性,以及原位PCR方法可能存在的问题和陷阱,包括与PCR产物扩散相关的假象以及标记核苷酸非特异性掺入正在修复的片段化DNA中。得出的结论是,该技术最终将在专业诊断实验室评估具有独特遗传标记的病毒性疾病、血液系统疾病和其他恶性肿瘤中发挥重要作用。