Robust one-Tube -PCR Strategy Accelerates Precise Sequence Modification of Plasmids for Functional Genomics

Functional genomics requires vector construction for protein expression and functional characterization of target genes; therefore, a simple, flexible and low-cost molecular manipulation strategy will be highly advantageous for genomics approaches. Here, we describe a -PCR strategy that enables multiple types of sequence modification, including precise insertion, deletion and substitution, in any position of a circular plasmid. -PCR is based on an overlap extension site-directed mutagenesis technique, and is named for its characteristic -shaped secondary structure during PCR. -PCR can be performed either in two steps, or in one tube in combination with exonuclease I treatment. These strategies have wide applications for protein engineering, gene function analysis and in vitro gene splicing.