Literature DB >> 7496531

The bacteriophage 434 operator/repressor system in yeast.

C I Webster1, W J Brammar.   

Abstract

The ability of the bacteriophage 434 operator/repressor system to function in a eukaryotic cell has been explored. An idealized 434 operator was placed at various positions in the PGK promoter of Saccharomyces cerevisiae: within the upstream activator sequence, close to the TATA box, and downstream of the transcription-initiation site. Expression of the 434 cI gene from a 2 microns-based plasmid resulted in significant repression of gene expression from constructs containing the altered promoters linked to a beta-galactosidase reporter gene. Attempts to use a variant of the 434 repressor that has the binding specificity of the P22 repressor (434P22) were unsuccessful, due to a severely inhibitory effect of this gene-product on the growth of the yeast cells.

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Year:  1995        PMID: 7496531     DOI: 10.1099/13500872-141-9-2191

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  2 in total

1.  Expression of a 434:VP16 chimeric activator leads to high-level activation of gene expression in stable transformants of Arabidopsis.

Authors:  Morten Storgaard; Thomas Didion; Finn Okkels; Klaus Kristian Nielse
Journal:  Transgenic Res       Date:  2002-04       Impact factor: 2.788

2.  A tight cold-inducible switch built by coupling thermosensitive transcriptional and proteolytic regulatory parts.

Authors:  Yang Zheng; Fankang Meng; Zihui Zhu; Weijia Wei; Zhi Sun; Jinchun Chen; Bo Yu; Chunbo Lou; Guo-Qiang Chen
Journal:  Nucleic Acids Res       Date:  2019-12-02       Impact factor: 16.971

  2 in total

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