Literature DB >> 23654272

Multichange isothermal mutagenesis: a new strategy for multiple site-directed mutations in plasmid DNA.

Leslie A Mitchell1, Yizhi Cai, Martin Taylor, Anne Marie Noronha, James Chuang, Lixin Dai, Jef D Boeke.   

Abstract

Multichange ISOthermal (MISO) mutagenesis is a new technique allowing simultaneous introduction of multiple site-directed mutations into plasmid DNA by leveraging two existing ideas: QuikChange-style primers and one-step isothermal (ISO) assembly. Inversely partnering pairs of QuikChange primers results in robust, exponential amplification of linear fragments of DNA encoding mutagenic yet homologous ends. These products are amenable to ISO assembly, which efficiently assembles them into a circular, mutagenized plasmid. Because the technique relies on ISO assembly, MISO mutagenesis is additionally amenable to other relevant DNA modifications such as insertions and deletions. Here we provide a detailed description of the MISO mutagenesis concept and highlight its versatility by applying it to three experiments currently intractable with standard site-directed mutagenesis approaches. MISO mutagenesis has the potential to become widely used for site-directed mutagenesis.

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Year:  2013        PMID: 23654272      PMCID: PMC4040258          DOI: 10.1021/sb300131w

Source DB:  PubMed          Journal:  ACS Synth Biol        ISSN: 2161-5063            Impact factor:   5.110


  13 in total

1.  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

2.  An efficient one-step site-directed and site-saturation mutagenesis protocol.

Authors:  Lei Zheng; Ulrich Baumann; Jean-Louis Reymond
Journal:  Nucleic Acids Res       Date:  2004-08-10       Impact factor: 16.971

3.  Enzymatic assembly of DNA molecules up to several hundred kilobases.

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4.  Constructing DNA by polymerase recombination.

Authors:  A A Yolov; Z A Shabarova
Journal:  Nucleic Acids Res       Date:  1990-07-11       Impact factor: 16.971

5.  Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition.

Authors:  Q Feng; J V Moran; H H Kazazian; J D Boeke
Journal:  Cell       Date:  1996-11-29       Impact factor: 41.582

6.  Precise gene fusion by PCR.

Authors:  J Yon; M Fried
Journal:  Nucleic Acids Res       Date:  1989-06-26       Impact factor: 16.971

7.  Complementary action of restriction enzymes endo R-DpnI and Endo R-DpnII on bacteriophage f1 DNA.

Authors:  G F Vovis; S Lacks
Journal:  J Mol Biol       Date:  1977-09-25       Impact factor: 5.469

8.  A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.

Authors:  R S Sikorski; P Hieter
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9.  An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesis protocol.

Authors:  Huanting Liu; James H Naismith
Journal:  BMC Biotechnol       Date:  2008-12-04       Impact factor: 2.563

10.  Golden gate shuffling: a one-pot DNA shuffling method based on type IIs restriction enzymes.

Authors:  Carola Engler; Ramona Gruetzner; Romy Kandzia; Sylvestre Marillonnet
Journal:  PLoS One       Date:  2009-05-14       Impact factor: 3.240

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  20 in total

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2.  Architectural organization of the metabolic regulatory enzyme ghrelin O-acyltransferase.

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Journal:  J Biol Chem       Date:  2013-09-17       Impact factor: 5.157

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.  Programmed evolution for optimization of orthogonal metabolic output in bacteria.

Authors:  Todd T Eckdahl; A Malcolm Campbell; Laurie J Heyer; Jeffrey L Poet; David N Blauch; Nicole L Snyder; Dustin T Atchley; Erich J Baker; Micah Brown; Elizabeth C Brunner; Sean A Callen; Jesse S Campbell; Caleb J Carr; David R Carr; Spencer A Chadinha; Grace I Chester; Josh Chester; Ben R Clarkson; Kelly E Cochran; Shannon E Doherty; Catherine Doyle; Sarah Dwyer; Linnea M Edlin; Rebecca A Evans; Taylor Fluharty; Janna Frederick; Jonah Galeota-Sprung; Betsy L Gammon; Brandon Grieshaber; Jessica Gronniger; Katelyn Gutteridge; Joel Henningsen; Bradley Isom; Hannah L Itell; Erica C Keffeler; Andrew J Lantz; Jonathan N Lim; Erin P McGuire; Alexander K Moore; Jerrad Morton; Meredith Nakano; Sara A Pearson; Virginia Perkins; Phoebe Parrish; Claire E Pierson; Sachith Polpityaarachchige; Michael J Quaney; Abagael Slattery; Kathryn E Smith; Jackson Spell; Morgan Spencer; Telavive Taye; Kamay Trueblood; Caroline J Vrana; E Tucker Whitesides
Journal:  PLoS One       Date:  2015-02-25       Impact factor: 3.240

5.  Development of a Tightly Controlled Off Switch for Saccharomyces cerevisiae Regulated by Camphor, a Low-Cost Natural Product.

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6.  Versatile genetic assembly system (VEGAS) to assemble pathways for expression in S. cerevisiae.

Authors:  Leslie A Mitchell; James Chuang; Neta Agmon; Chachrit Khunsriraksakul; Nick A Phillips; Yizhi Cai; David M Truong; Ashan Veerakumar; Yuxuan Wang; María Mayorga; Paul Blomquist; Praneeth Sadda; Joshua Trueheart; Jef D Boeke
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7.  Patch cloning method for multiple site-directed and saturation mutagenesis.

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9.  One-Tube-Only Standardized Site-Directed Mutagenesis: An Alternative Approach to Generate Amino Acid Substitution Collections.

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10.  Gibson Deletion: a novel application of isothermal in vitro recombination.

Authors:  Swara Kalva; Jef D Boeke; Paolo Mita
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