Zuo Zhuang, Jabbar Kausar J
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Unit 72, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Methods Mol Biol. 2016;1392:17-25. doi: 10.1007/978-1-4939-3360-0_2.
Co-amplification at lower denaturation temperature-based polymerase chain reaction (COLD-PCR) is a single-step amplification method that results in the enhancement of both known and unknown minority alleles during PCR, irrespective of mutation type and position. This method is based on exploitation of the critical temperature, Tc, at which mutation-containing DNA is preferentially melted over wild type. COLD-PCR can be a good strategy for mutation detection in specimens with high nonneoplastic cell content, small specimens in which neoplastic cells are difficult to micro-dissect and therefore enrich, and whenever a mutation is suspected to be present but is undetectable using conventional PCR and sequencing methods. We describe in this chapter our COLD-PCR-based pyrosequencing method for KRAS mutation detection in various clinical samples using DNA extracted from either fresh or fixed paraffin-embedded tissue specimens.
基于较低变性温度的聚合酶链反应(COLD-PCR)共扩增是一种单步扩增方法,可在PCR过程中增强已知和未知的少数等位基因,而与突变类型和位置无关。该方法基于对临界温度Tc的利用,在该温度下,含突变的DNA比野生型DNA优先解链。对于非肿瘤细胞含量高的标本、难以进行微切割和富集肿瘤细胞的小标本,以及怀疑存在突变但使用传统PCR和测序方法无法检测到的情况,COLD-PCR可能是一种很好的突变检测策略。在本章中,我们描述了基于COLD-PCR的焦磷酸测序方法,用于使用从新鲜或固定石蜡包埋组织标本中提取的DNA检测各种临床样本中的KRAS突变。