Literature DB >> 15767700

A single-stage polymerase-based protocol for the introduction of deletions and insertions without subcloning.

John C Salerno1, Rachel J Jones, Eda Erdogan, Susan M E Smith.   

Abstract

A single-stage polymerase-based procedure is described that allows extensive modifications of DNA. The version described here uses the QuikChange Site-Directed Mutagenesis System kit supplied by Stratagene. The original protocol is replaced by a single-stage method in which linear production of complementary strands is accomplished in separate single primer reactions. This has proved effective in introducing insertions and deletions into large gene/vector combinations without subcloning.

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Year:  2005        PMID: 15767700     DOI: 10.1385/MB:29:3:225

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  8 in total

1.  Generation of deletion and point mutations with one primer in a single cloning step.

Authors:  O Makarova; E Kamberov; B Margolis
Journal:  Biotechniques       Date:  2000-11       Impact factor: 1.993

2.  Integration of PCR fragments at any specific site within cloning vectors without the use of restriction enzymes and DNA ligase.

Authors:  M Geiser; R Cèbe; D Drewello; R Schmitz
Journal:  Biotechniques       Date:  2001-07       Impact factor: 1.993

3.  Two-stage polymerase chain reaction protocol allowing introduction of multiple mutations, deletions, and insertions, using QuikChange site-directed mutagenesis.

Authors:  Wenyan Wang; Bruce A Malcolm
Journal:  Methods Mol Biol       Date:  2002

4.  Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange Site-Directed Mutagenesis.

Authors:  W Wang; B A Malcolm
Journal:  Biotechniques       Date:  1999-04       Impact factor: 1.993

Review 5.  Site-directed mutagenesis in vitro by megaprimer PCR.

Authors:  S Barik
Journal:  Methods Mol Biol       Date:  1996

6.  The "megaprimer" method of site-directed mutagenesis.

Authors:  G Sarkar; S S Sommer
Journal:  Biotechniques       Date:  1990-04       Impact factor: 1.993

7.  Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction.

Authors:  K Mullis; F Faloona; S Scharf; R Saiki; G Horn; H Erlich
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1986

8.  Modification of the megaprimer method of PCR mutagenesis: improved amplification of the final product.

Authors:  A Aiyar; J Leis
Journal:  Biotechniques       Date:  1993-03       Impact factor: 1.993

  8 in total
  4 in total

1.  INSULT: a novel mutagenesis method generating high yields of closed circular mutant DNA with one primer per mutant.

Authors:  Eda Erdogan; Rachel J Jones; P Matzlin; Michael H Hanna; Susan M E Smith; John C Salerno
Journal:  Mol Biotechnol       Date:  2005-05       Impact factor: 2.695

2.  Identification of a new motif in family B DNA polymerases by mutational analyses of the bacteriophage t4 DNA polymerase.

Authors:  Vincent Li; Matthew Hogg; Linda J Reha-Krantz
Journal:  J Mol Biol       Date:  2010-05-21       Impact factor: 5.469

Review 3.  Strategies used for genetically modifying bacterial genome: site-directed mutagenesis, gene inactivation, and gene over-expression.

Authors:  Jian-zhong Xu; Wei-guo Zhang
Journal:  J Zhejiang Univ Sci B       Date:  2016-02       Impact factor: 3.066

4.  A rare variant in MCF2L identified using exclusion linkage in a pedigree with premature atherosclerosis.

Authors:  Stephanie Maiwald; Mahdi M Motazacker; Julian C van Capelleveen; Suthesh Sivapalaratnam; Allard C van der Wal; Chris van der Loos; John J P Kastelein; Willem H Ouwehand; G Kees Hovingh; Mieke D Trip; Jaap D van Buul; Geesje M Dallinga-Thie
Journal:  Eur J Hum Genet       Date:  2015-04-22       Impact factor: 4.246

  4 in total

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