An improved PCR-mutagenesis strategy for two-site mutagenesis or sequence swapping between related genes

Nucleic Acids Res. 1998 Apr 1;26(7):1848-50. doi: 10.1093/nar/26.7.1848.

Abstract

The QuikChangeTM protocol is one of the simplest and fastest methods for site-directed mutagenesis, but introduces mutations at only one site at a time, and requires two HPLC-purified complementary oligonucleotides. Here, we describe that this method can be used with non-overlapping oligonucleotides. By doing this, two separate sites can be mutagenised simultaneously, or money can be saved by using a second 'standard' oligonucleotide. By a further modification, we have also used the QuikChangeTM approach to exchange DNA sequences between closely related genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Animals
  • Base Sequence
  • COS Cells
  • Chromatography, High Pressure Liquid
  • DNA / chemistry
  • DNA / metabolism
  • DNA Primers / chemistry
  • Mutagenesis, Site-Directed*
  • Oligodeoxyribonucleotides / chemistry
  • Oligodeoxyribonucleotides / isolation & purification
  • Plasmids
  • Point Mutation
  • Polymerase Chain Reaction / methods*
  • Reproducibility of Results
  • Transfection

Substances

  • DNA Primers
  • Oligodeoxyribonucleotides
  • DNA