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Biotechnology & Immunology

Overview: High Efficiency Oligonucleotide-Directed Mutagenesis of Double-stranded DNA Vectors

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Pages 1023-1029 | Published online: 02 Mar 2011

References to Primary Literature

  • McPherson MJ Directed Mutagenesis: A Practical Approach IRL Press at Oxford University Press Oxford 1991.
  • Shaw WV The design, synthesis and characterisation of factitious proteins. Biochem. J. 1987 246 1–17.
  • Schimmel P Hazards and their exploitation in the applications of molecular biology to structure-function relationships. Biochemistry 1990 29 9495–9502.
  • Chiou SH, Hu MC, Chung B A missense mutation at Ile172-Asn or Arg356-Trp causes steroid 21-hydroxylase deficiency. J. Biol. Chem. 1990 265 3549–3552.
  • Glade T, Englisch U Oligonucleotidedirected mutagenesis of the E. coli His gene. Nucleosides and Nucleotides 1988 7 741–744.
  • Sayers JR, Eckstein F A single-strand specific endonuclease activity co-purifies with overexpressed T5 D15 exonuclease. Nucleic Acids Res. 1991 19 4127–4132.
  • Cheng YSE, McGowan MH, Kettner CA, Schloss JV, Erickson-Viitanen S, Yin FH High-level expression of recombinant HIV-1 protease and the recovery of active enzyme from inclusion bodies. Gene 1990 87 243–248.
  • Hellman J, Mantsala P Construction of an Escherichia-coli export-affinity vector for the expression and purification of foreign proteins by fusion to cyclomaltodextrin glucanotransferase. J. Biotechnology 1992 23 19–34.
  • Nilsson B, Abrahmsen L, Uhlen M Immobilization and purification of enzymes with Staphylococcal protein-A gene fusion vectors. EMBO J. 1985 4 1075–1080.
  • Maina CV, Riggs PD, Grandia AG, Slatko BE, Moran LS, Tagliamonte JA, McReynolds LA, Diguan C An Escherichia-coli vector to express and purify foreign proteins by fusion to and separation from maltose-binding protein. Gene 1988 74 365–373.
  • Markmeyer P, Ruhlmann A, Englisch U, Kramer F The pAX plasmids - new gene-fusion vectors for sequencing, mutagenesis and expression of proteins in. Escherichia coli. Gene 1990 93 129–134.
  • Shen SH Multiple joined genes prevent product degradation in Escherichia coli.. Proc. Natl. Acad. Sci. USA 1984 81 4627–4631.
  • Smith M In vitro mutagenesis. Ann. Rev. Biochem. 1985 19 423–462.
  • Blacklow SC, Knowles JR Spiked oligonucleotide mutagenesis 163–196 [1].
  • Frank R, Meyerhans A, Schwellnus K, Blocker H Simultaneous synthesis and biological applications of DNA fragments - an efficient and complete methodology. Methods Enzymol. 1987 154 221–249.
  • Richards JH Cassette mutagenesis 163–196 In [1].
  • Modrich P Methyl-directed DNA mismatch correction. J. Biol. Chem. 1989 264 6597–6560.
  • Kunkel TA Rapid and efficient site-specific mutagenesis without phenotypic selection. Proc. Natl. Acad. Sci. USA 1985 82 488–492.
  • Hofer B, Kuehlein B A high efficiency method for site-directed mutagenesis with any plasmid. Gene 1989 84 153–157.
  • Slilaty SN, Fung M, Shen SH, Lebel S Site-directed mutagenesis by complementarystrand synthesis using a closing oligonucleotide and double-stranded DNA templates. Analytical Biochem. 1990 185 194–200.
  • Sayers JR, Eckstein F Phosphorothioatebased site-directed mutagenesis for single-stranded vectors 49–69 In [1].
  • Nakamaye K, Eckstein F Inhibition of restriction endonuclease NciI cleavage by phosphorothioate groups and its application to oligonucleotide-directed mutagenesis. Nucleic Acids Res. 1986 14 9679–9698.
  • Sayers JR, Krekel C, Eckstein F Rapid high efficiency site-directed mutagenesis via the phosphorothioate approach. Biotechniques 1992 In press.
  • Olsen DB, Eckstein F High-efficiency oligonucleotide-directed plasmid mutagenesis. Proc. Natl. Acad. Sci. USA 1990 87 1451–1455.
  • Olsen DB, Eckstein F Phosphorothioate based double-stranded plasmid mutagenesis 83–99 In [1].
  • Olsen DB, Sayers JR, Eckstein F Site-Directed Mutagenesis of Single and Double-Stranded DNA. Recombinant DNA: Methods in Enzymology Wu R Academic Press Inc San Diego In press.
  • Sugimoto M, Esaki N, Tanaka H, Soda K A simple and efficient method for the oligonucleotide-directed mutagenesis using plasmid DNA template and phosphorothioate-modified nucleotide. Analytical Biochem. 1989 179 309–311.
  • Palermo DP, Hess GF Use of lambda exonuclease for the efficient oligonucleotidemediated site-directed deletion and point mutation of double-stranded DNA. DNA 1987 6 273–279.
  • Bellini AV, De Ferra F, Grandi G A rapid and versatile site-directed method of mutagenesis for double stranded plasmid DNA. Gene 1988 69 325–330.
  • Mullis K, Faloona F, Scharf S, Saiki R, Horn G, Erlich H Specific enzymatic amplification of DNA in vitro - the polymerase chain reaction. Cold Spring Harbor Symposia on Quantiative Biology 1986 51P1 262–273.
  • Dulau L, Cheyrou A, Aigle M Directed mutagenesis using PCR. Nucleic Acids Res. 1989 17 2873.
  • Hemsley A, Arnheim M, Toney MD, Cortopasi G, Galas DJ A simple method for site-directed mutagenesis using the polymerase chain reaction. Nucleic Acids Res. 1989 17 6545–6551.
  • Karlovsky P Misuse of PCR. Trends in Biochem. Sci. 15 419.
  • Keohavong P, Thilly WG Fidelity of DNA polymerases in DNA amplification. Proc. Natl. Acad. Sci. USA 1989 86 9253–9257.
  • Cariello NF, Thilly WG, Swenberg JA, Skopek TR Deletion mutagenesis during polymerase chain reaction: Dependence on DNA polymerase. Gene 1991 99 105–108.
  • Brakenhoff RH, Schoenmakers JGG, Lubsen NH Chimeric cDNA clones: A novel PCR artefact. Nucleic Acids Res. 1991 19 1949.
  • Hultmann T, Murby M, Stahl S, Hornes E, Uhlen M Solid phase in vitro mutagenesis using plasmid DNA template. Nucleic Acids Res. 1990 18 5107–5112.
  • Kammann M, Laufs J, Schell J, Gronenborn B Rapid insertional mutagenesis by polymerase chain reaction (PCR). Nucleic Acids Res. 1989 17 5404.
  • Zhou Y, Zhang X, Ebright RH Random mutagenesis of gene-sized DNA molecules by use of PCR with Taq DNA polymerase. Nucleic Acids Res. 1991 19 6052.
  • Brown T, Brown DJS Modern machineaided methods of oligonucleotide synthesis 1–23.

References to Patent Literature

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