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Book ChapterDOI

Vectors for constitutive and inducible gene expression in yeast.

Mark Schena, +2 more
- 01 Jan 1991 - 
- Vol. 194, pp 389-398
TLDR
Three new plasmids are constructed that direct high-level constitutive gene expression in yeast that contain the very efficient yeast glyceraldehyde-3-phosphate dehydrogenase promoter.
Abstract
Publisher Summary This chapter describes vector systems for constitutive and inducible gene expression in Saccharomyces cerevisiae . Three new plasmids (pG-1, pG-2, and pG-3) are constructed that direct high-level constitutive gene expression in yeast. These vectors, derived from plasmids originally developed for expression of the rat glucocorticoid receptor cDNA in yeast, contain the very efficient yeast glyceraldehyde-3-phosphate dehydrogenase promoter. Each plasmid contains the yeast TRPI gene and 2-μm origin of replication and the ampicillin resistance gene and prokaryotic origin of replication from pUC18. In addition, a hormone-inducible expression vector is discussed in the chapter whose low basal promoter activity is strongly enhanced by the addition of glucocorticoids to yeast cells expressing the glucocorticoid receptor.

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Citations
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Hsp104, Hsp70, and Hsp40: A Novel Chaperone System that Rescues Previously Aggregated Proteins

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Foreign gene expression in yeast: a review.

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The saccharomyces cerevisiae zinc finger proteins msn2p and msn4p are required for transcriptional induction through the stress-response element (stre )

TL;DR: The results suggest that MSN2 and MSN4 encode a DNA‐binding component of the stress responsive system and it is likely that they act as positive transcription factors.
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Nuclear Localization of NPR1 Is Required for Activation of PR Gene Expression

TL;DR: It is clearly demonstrate that nuclear localization of NPR1 is essential for its activity in inducing PR genes.
References
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Journal ArticleDOI

Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors

TL;DR: New Escherichia coli host strains have been constructed for the E. coli bacteriophage M13 and the high-copy-number pUC-plasmid cloning vectors and mutations introduced into these strains improve cloning of unmodified DNA and of repetitive sequences.
Journal ArticleDOI

Transformation of intact yeast cells treated with alkali cations.

TL;DR: The transformation efficiency with Cs+ or Li+ was comparable with that of conventional protoplast methods for a plasmid containing ars1, although not for plasmids containing a 2 microns origin replication.
Journal ArticleDOI

Transformation of intact yeast cells treated with alkali cations or thiol compounds

TL;DR: The transformation efficiency with Cs+ or Li+ was comparable with that of conventional protoplast methods for a plasmid containing ars1, although not for plasmids containing a 2 microns origin replication.
Journal ArticleDOI

Steroid Receptor Regulated Transcription of Specific Genes and Gene Networks

TL;DR: Information is provided on how to identify the Steroid Receptors, Receptor Binding Sites, and other mechanisms that aid in the identification of the receptors and their locations in the genome.
Journal ArticleDOI

Sequences that regulate the divergent GAL1-GAL10 promoter in Saccharomyces cerevisiae.

TL;DR: The GAL1 and GAL10 genes of Saccharomyces cerevisiae are divergently transcribed, with 606 base pairs of DNA separating their transcription initiation sites as mentioned in this paper.
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