Kumar Raj, Rajagopal Kammara
Institute of Microbial Technology, Chandigarh 160036, India.
Anal Biochem. 2008 Jun 1;377(1):105-7. doi: 10.1016/j.ab.2008.03.003. Epub 2008 Mar 7.
We present a simple, single-step, single-tube, and rapid method for introducing a series of mutations into cloned DNA. Polymerase chain reaction (PCR)-based mutagenesis methods have become very prevalent due to their simplicity and efficiency for introducing mutations. Our method, overlap-primer-walk PCR, has several advantages over other published methods. It uses two common oligodeoxyribonucleotides and a series of overlapping primers specific for various mutations. Once common flanking primers are selected, two to three mutations require only one additional primer. Therefore, this method is very useful for introduction of multiple mutations in various sites of the target DNA. We illustrate the usefulness of the method by introducing several mutations into the human TNF-alpha encoding gene.
我们提出了一种简单、单步、单管且快速的方法,用于将一系列突变引入克隆的DNA中。基于聚合酶链反应(PCR)的诱变方法因其引入突变的简便性和高效性而变得非常普遍。我们的方法,即重叠引物步移PCR,相对于其他已发表的方法具有几个优点。它使用两个通用的寡脱氧核糖核苷酸和一系列针对各种突变的重叠引物。一旦选择了通用的侧翼引物,两到三个突变仅需额外一个引物。因此,该方法对于在目标DNA的各个位点引入多个突变非常有用。我们通过将几个突变引入人TNF-α编码基因来说明该方法的实用性。