Kraytsberg Yevgenya, Khrapko Konstantin
Beth Israel Deaconess Medical Center & Harvard Medical School, 21-27 Burlington Avenue, Boston, MA 02215, USA.
Expert Rev Mol Diagn. 2005 Sep;5(5):809-15. doi: 10.1586/14737159.5.5.809.
A critical review of the clone-by-clone approach to the analysis of complex spectra of somatic mutations is presented. The study of a priori unknown somatic mutations requires painstaking analysis of complex mixtures of multiple mutant and non-mutant DNA molecules. If mutant fractions are sufficiently high, these mixtures can be dissected by the cloning of individual DNA molecules and scanning of the individual clones for mutations (e.g., by sequencing). Currently, the majority of such cloning is performed using PCR fragments. However, post-PCR cloning may result in various PCR artifacts - PCR errors and jumping PCR - and preferential amplification of certain mutations. This review argues that single-molecule PCR is a simple alternative that promises to evade the disadvantages inherent to post-PCR cloning and enhance mutational analysis in the future.
本文对用于分析体细胞突变复杂谱的逐个克隆方法进行了批判性综述。对先验未知的体细胞突变进行研究,需要对多个突变和非突变DNA分子的复杂混合物进行细致分析。如果突变比例足够高,这些混合物可以通过单个DNA分子的克隆以及对单个克隆进行突变扫描(例如通过测序)来剖析。目前,大多数此类克隆是使用PCR片段进行的。然而,PCR后克隆可能会导致各种PCR假象——PCR错误和跳跃PCR——以及某些突变的优先扩增。本综述认为,单分子PCR是一种简单的替代方法,有望避免PCR后克隆固有的缺点,并在未来增强突变分析。