Literature DB >> 2500675

Versatile cassettes designed for the copper inducible expression of proteins in yeast.

I G Macreadie1, M N Jagadish, A A Azad, P R Vaughan.   

Abstract

A series of yeast expression vectors and cassettes utilizing the CUP1 gene of Saccharomyces cerevisiae have been constructed. The cassettes contain multiple cloning sites for gene fusions and were created by inserting a 27-bp polylinker at the +14 position of the CUP1 gene. The cassettes are portable as restriction fragments and enable copper-regulated expression of foreign proteins in S. cerevisiae. In copper sensitive yeast, multiple copies of the CUP1 cassettes confer copper resistance due to the production of the copper metallothionein. Genes cloned into the CUP1 cassettes, however, usually prevent translation of the metallothionein leading to a loss of resistance. This could be useful for one-step cloning into yeast.

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Year:  1989        PMID: 2500675     DOI: 10.1016/0147-619x(89)90059-0

Source DB:  PubMed          Journal:  Plasmid        ISSN: 0147-619X            Impact factor:   3.466


  9 in total

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Authors:  W F Tam; L H Lee; L Davis; R Sen
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

2.  Yeast vectors for cloning and copper-inducible expression of foreign genes.

Authors:  I G Macreadie
Journal:  Nucleic Acids Res       Date:  1990-02-25       Impact factor: 16.971

3.  The Saccharomyces cerevisiae homologues of endonuclease III from Escherichia coli, Ntg1 and Ntg2, are both required for efficient repair of spontaneous and induced oxidative DNA damage in yeast.

Authors:  I Alseth; L Eide; M Pirovano; T Rognes; E Seeberg; M Bjørås
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

4.  Targeting of Tsc13p to nucleus-vacuole junctions: a role for very-long-chain fatty acids in the biogenesis of microautophagic vesicles.

Authors:  Erik Kvam; Kenneth Gable; Teresa M Dunn; David S Goldfarb
Journal:  Mol Biol Cell       Date:  2005-06-15       Impact factor: 4.138

5.  Analysis of the chromosomal DNA polymorphism of wine strains of Saccharomyces cerevisiae.

Authors:  C Bidenne; B Blondin; S Dequin; F Vezinhet
Journal:  Curr Genet       Date:  1992-07       Impact factor: 3.886

6.  Nucleus-vacuole junctions in Saccharomyces cerevisiae are formed through the direct interaction of Vac8p with Nvj1p.

Authors:  X Pan; P Roberts; Y Chen; E Kvam; N Shulga; K Huang; S Lemmon; D S Goldfarb
Journal:  Mol Biol Cell       Date:  2000-07       Impact factor: 4.138

7.  Methods for measuring misfolded protein clearance in the budding yeast Saccharomyces cerevisiae.

Authors:  Rahul S Samant; Judith Frydman
Journal:  Methods Enzymol       Date:  2019-02-08       Impact factor: 1.600

8.  Conversion of deoxynivalenol to 3-acetyldeoxynivalenol in barley-derived fuel ethanol co-products with yeast expressing trichothecene 3-O-acetyltransferases.

Authors:  Piyum A Khatibi; Justin Montanti; Nhuan P Nghiem; Kevin B Hicks; Greg Berger; Wynse S Brooks; Carl A Griffey; David G Schmale
Journal:  Biotechnol Biofuels       Date:  2011-09-02       Impact factor: 6.040

9.  A versatile plasmid system for reconstitution and analysis of mammalian ubiquitination cascades in yeast.

Authors:  Rossella Avagliano Trezza; Janny van den Burg; Nico van den Oever; Ben Distel
Journal:  Microb Cell       Date:  2017-12-05
  9 in total

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