Fromant M, Blanquet S, Plateau P
Laboratoire de Biochimie, URA 240 CNRS, Ecole Polytechnique, Palaiseau, France.
Anal Biochem. 1995 Jan 1;224(1):347-53. doi: 10.1006/abio.1995.1050.
The polymerase chain reaction (PCR) can be used to amplify a DNA fragment with the concomitant creation of numerous mutations provided that one dNTP substrate is in excess over the three others. Advantage was taken of this behavior to systematically mutagenize a 291-bp-long DNA fragment and to define the rules relating the frequencies of each possible bp substitution to the set of the dNTP concentrations in the PCR experiment. Sets of parameters governing the rules were determined under various mutagenic conditions including the addition of MnCl2. Finally, validity of the rules was assessed in several mutagenesis experiments showing that a wide range of substitution frequencies including AT-->GC and GC-->AT transitions as well as AT-->TA transversions can be obtained at will.
聚合酶链反应(PCR)可用于扩增DNA片段,前提是一种脱氧核苷酸三磷酸(dNTP)底物的量超过其他三种底物,同时会产生大量突变。利用这一特性,对一个291bp长的DNA片段进行了系统性诱变,并确定了在PCR实验中每种可能的碱基替换频率与dNTP浓度之间的关系规则。在包括添加氯化锰(MnCl₂)在内的各种诱变条件下,确定了控制这些规则的参数集。最后,在多个诱变实验中评估了这些规则的有效性,结果表明可以随意获得包括AT→GC和GC→AT转换以及AT→TA颠换在内的广泛替换频率。