Construction of a cytosolic firefly luciferase reporter cassette for use in PCR-mediated gene deletion and fusion inSaccharomyces cerevisiae-Reference-Cited by-同舟云学术

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Construction of a cytosolic firefly luciferase reporter cassette for use in PCR-mediated gene deletion and fusion inSaccharomyces cerevisiae

Published:2012-11-21 Issue:12 Volume:29 Page:505-517
ISSN:0749-503X
Container-title:Yeast
language:en
Short-container-title:Yeast

Author:

Ainsworth W. B.¹,Rome C. M.¹,Hjortsø M. A.¹,Benton M. G.¹

Affiliation:

1. Cain Department of Chemical Engineering; Louisiana State University; Baton Rouge; LA; 70803; USA

Publisher

Wiley

Subject

Genetics,Applied Microbiology and Biotechnology,Biochemistry,Bioengineering,Biotechnology

Reference42 articles.

1. Application of yeast cells transformed with GFP expression constructs containing the RAD54 or RNR2 promoter as a test for the genotoxic potential of chemical substances;Afanassiev;Mutat Res,2000

2. The utilization of a Saccharomyces cerevisiae HUG1P-GFP promoter-reporter construct for the selective detection of DNA damage;Benton;Mutat Res,2007

3. Photinus pyralis luciferase: vectors that contain a modified luc coding sequence allowing convenient transfer into other systems;Bonin;Gene,1994

4. Development of RNR3- and RAD54-GUS reporters for testing genotoxicity in Saccharomyces cerevisiae;Boronat;Anal Bioanal Chem,2006

5. Saccharomyces cerevisiae JEN1 promoter activity is inversely related to concentration of repressing sugar;Chambers;Appl Environ Microbiol,2004

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1. Identification of different classes of genome instability suppressor genes through analysis of DNA damage response markers;G3: Genes, Genomes, Genetics;2024-03-25

2. Identification of different classes of genome instability suppressor genes through analysis of DNA damage response markers;2022-03-01

3. A Random Screen Using a Novel Reporter Assay System Reveals a Set of Sequences That Are Preferred as the TATA or TATA-Like Elements in the CYC1 Promoter of Saccharomyces cerevisiae;PLOS ONE;2015-06-05

4. Cytoplasmic localization of Hug1p, a negative regulator of the MEC1 pathway, coincides with the compartmentalization of Rnr2p–Rnr4p;Biochemical and Biophysical Research Communications;2013-10

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