Literature DB >> 8074874

Recycling selectable markers in yeast.

B Sauer1.   

Abstract

A series of excisable marker cassettes has been constructed to facilitate recycling of selectable markers in yeast. These cassettes exploit the use of the Cre DNA recombinase to precisely excise the marker gene when desired. They are especially useful for making gene disruptions and then removing the marker gene to allow subsequent genetic manipulations with that same marker. Also described are a number of cre expression vectors that allow galactose-induced expression of the recombinase in yeast. The procedure is simple and allows rapid processing of large numbers of transformants.

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Year:  1994        PMID: 8074874

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  14 in total

1.  Simultaneous Cre catalyzed recombination of two alleles to restore neomycin sensitivity and facilitate homozygous mutations.

Authors:  D S Milstone; G Bradwin; R M Mortensen
Journal:  Nucleic Acids Res       Date:  1999-08-01       Impact factor: 16.971

2.  Convenient and reversible site-specific targeting of exogenous DNA into a bacterial chromosome by use of the FLP recombinase: the FLIRT system.

Authors:  L C Huang; E A Wood; M M Cox
Journal:  J Bacteriol       Date:  1997-10       Impact factor: 3.490

3.  A new efficient gene disruption cassette for repeated use in budding yeast.

Authors:  U Güldener; S Heck; T Fielder; J Beinhauer; J H Hegemann
Journal:  Nucleic Acids Res       Date:  1996-07-01       Impact factor: 16.971

4.  Recycling selectable markers in mouse embryonic stem cells.

Authors:  A Abuin; A Bradley
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

5.  Dual targeting of Osh1p, a yeast homologue of oxysterol-binding protein, to both the Golgi and the nucleus-vacuole junction.

Authors:  T P Levine; S Munro
Journal:  Mol Biol Cell       Date:  2001-06       Impact factor: 4.138

6.  A new method for repeated "self-cloning" promoter replacement in Saccharomyces cerevisiae.

Authors:  Olga A Sofyanovich; Hiroaki Nishiuchi; Kazuo Yamagishi; Kenjiro Maekawa; Vsevolod A Serebryanyy
Journal:  Mol Biotechnol       Date:  2011-07       Impact factor: 2.695

7.  Repetitive, marker-free, site-specific integration as a novel tool for multiple chromosomal integration of DNA.

Authors:  Kia Vest Petersen; Jan Martinussen; Peter Ruhdal Jensen; Christian Solem
Journal:  Appl Environ Microbiol       Date:  2013-03-29       Impact factor: 4.792

8.  A vector set for systematic metabolic engineering in Saccharomyces cerevisiae.

Authors:  Fang Fang; Kirsty Salmon; Michael W Y Shen; Kimberly A Aeling; Elaine Ito; Becky Irwin; Uyen Phuong C Tran; G Wesley Hatfield; Nancy A Da Silva; Suzanne Sandmeyer
Journal:  Yeast       Date:  2010-10-08       Impact factor: 3.239

9.  Retromer and the sorting nexins Snx4/41/42 mediate distinct retrieval pathways from yeast endosomes.

Authors:  Ewald H Hettema; Michael J Lewis; Michael W Black; Hugh R B Pelham
Journal:  EMBO J       Date:  2003-02-03       Impact factor: 11.598

Review 10.  Strategies to achieve conditional gene mutation in mice.

Authors:  Jessica J Gierut; Tyler E Jacks; Kevin M Haigis
Journal:  Cold Spring Harb Protoc       Date:  2014-04-01
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