GENE-SPLICING BY OVERLAP EXTENSION - TAILOR-MADE GENES USING THE POLYMERASE CHAIN-REACTION
- 1 May 1990
- journal article
- research article
- Vol. 8 (5) , 528-+
Abstract
Gene Splicing by Overlap Extension or "gene SOEing" is a PCR-based method of recombining DNA sequences without reliance on restriction sites and of directly generating mutated DNA fragments in vitro. By modifying the sequences incorporated into the 5''-ends of the primers, any pair of polymerase chain reaction products can be made to share a common sequence at one end. Under polymerase chain reaction conditions, the common sequence allows strands from two different fragments to hybridize to one another, forming an overlap. Extension of this overlap by DNA polymerase yields a recombinant molecule. This powerful and technically simple approach offers many advantages over conventional approaches for manipulating gene sequences.This publication has 7 references indexed in Scilit:
- Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extensionPublished by Elsevier ,2003
- THE MEGAPRIMER METHOD OF SITE-DIRECTED MUTAGENESIS1990
- The functional significance of two amino acid polymorphisms in the antigen-presenting domain of class I MHC molecules. Molecular dissection of Kbm3.The Journal of Immunology, 1989
- Use of polymerase chain reaction catalyzed by Taq DNA polymerase for site-specific mutagenesisGene, 1989
- A general method ofin vitropreparation and specific mutagenesis of DNA fragments: study of protein and DNA interactionsNucleic Acids Research, 1988
- Sequence analysis and structure-function correlations of murine q, k, u, s, and f haplotype I-A beta cDNA clones.Proceedings of the National Academy of Sciences, 1986
- Regions of allelic hypervariability in the murine Aα immune response geneCell, 1983