Literature DB >> 2179950

Mutations that increase the activity of a transcriptional activator in yeast and mammalian cells.

G Gill1, I Sadowski, M Ptashne.   

Abstract

Activating region I of GAL4 protein is a stretch of amino acids, positioned adjacent to the DNA-binding region, that activates transcription in yeast and, as we show here, in mammalian cells. Here we describe mutations located throughout a 65-amino acid region that increase the activation function of region I. Most of these mutations replace positively charged amino acids in the region with neutral ones, although we also describe substitutions at one position that do not alter the charge of the region. Mutations of region I that alter the activation function in yeast have similar effects on activation when assayed in mammalian cells. When individual mutations that raise the acidity of the activating region are recombined, the activities of the mutant proteins increase with increasing negative charge in both yeast and mammalian cells. These results extend and modify the correlation between acidity and activation and suggest that the requirements for a strong activating region are conserved in yeast and mammals.

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Year:  1990        PMID: 2179950      PMCID: PMC53639          DOI: 10.1073/pnas.87.6.2127

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  38 in total

1.  Transcription activation by the adenovirus E1a protein.

Authors:  J W Lillie; M R Green
Journal:  Nature       Date:  1989-03-02       Impact factor: 49.962

2.  A single glutamic acid residue plays a key role in the transcriptional activation function of lambda repressor.

Authors:  F D Bushman; C Shang; M Ptashne
Journal:  Cell       Date:  1989-09-22       Impact factor: 41.582

3.  Specific protein binding to far upstream activating sequences in polymerase II promoters.

Authors:  R J Bram; R D Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

4.  Repressor structure and the mechanism of positive control.

Authors:  A Hochschild; N Irwin; M Ptashne
Journal:  Cell       Date:  1983-02       Impact factor: 41.582

5.  Primary structure of the Saccharomyces cerevisiae GAL4 gene.

Authors:  A Laughon; R F Gesteland
Journal:  Mol Cell Biol       Date:  1984-02       Impact factor: 4.272

6.  Mapping of multiple phosphorylation sites within the structural and catalytic domains of the Fujinami avian sarcoma virus transforming protein.

Authors:  G Weinmaster; E Hinze; T Pawson
Journal:  J Virol       Date:  1983-04       Impact factor: 5.103

7.  A GAL10-CYC1 hybrid yeast promoter identifies the GAL4 regulatory region as an upstream site.

Authors:  L Guarente; R R Yocum; P Gifford
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

8.  Transformation of intact yeast cells treated with alkali cations.

Authors:  H Ito; Y Fukuda; K Murata; A Kimura
Journal:  J Bacteriol       Date:  1983-01       Impact factor: 3.490

9.  Expression and regulation of Escherichia coli lacZ gene fusions in mammalian cells.

Authors:  C V Hall; P E Jacob; G M Ringold; F Lee
Journal:  J Mol Appl Genet       Date:  1983

10.  Saccharomyces cerevisiae GAL1-GAL10 divergent promoter region: location and function of the upstream activating sequence UASG.

Authors:  R W West; R R Yocum; M Ptashne
Journal:  Mol Cell Biol       Date:  1984-11       Impact factor: 4.272

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  24 in total

1.  The MRF4 activation domain is required to induce muscle-specific gene expression.

Authors:  K L Mak; R Q To; Y Kong; S F Konieczny
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

2.  A genetic system for studying the activity of a proteolytic enzyme.

Authors:  B Dasmahapatra; B DiDomenico; S Dwyer; J Ma; I Sadowski; J Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-01       Impact factor: 11.205

3.  Activating regions of yeast transcription factors must have both acidic and hydrophobic amino acids.

Authors:  D M Ruden
Journal:  Chromosoma       Date:  1992-03       Impact factor: 4.316

Review 4.  Functional assays for BRCA1 and BRCA2.

Authors:  Marcelo A Carvalho; Fergus J Couch; Alvaro N A Monteiro
Journal:  Int J Biochem Cell Biol       Date:  2006-08-18       Impact factor: 5.085

5.  Quantitation of putative activator-target affinities predicts transcriptional activating potentials.

Authors:  Y Wu; R J Reece; M Ptashne
Journal:  EMBO J       Date:  1996-08-01       Impact factor: 11.598

6.  Extensive mutagenesis of a transcriptional activation domain identifies single hydrophobic and acidic amino acids important for activation in vivo.

Authors:  M B Sainz; S A Goff; V L Chandler
Journal:  Mol Cell Biol       Date:  1997-01       Impact factor: 4.272

7.  An artificial transcriptional activating region with unusual properties.

Authors:  X Lu; A Z Ansari; M Ptashne
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-29       Impact factor: 11.205

8.  Gene regulation in microbial eukaryotes in the early 1990s.

Authors:  H N Arst
Journal:  World J Microbiol Biotechnol       Date:  1992-12       Impact factor: 3.312

9.  Comparing regions of the Epstein-Barr virus ZEBRA protein which function as transcriptional activating sequences in Saccharomyces cerevisiae and in B cells.

Authors:  G Miller; H Himmelfarb; L Heston; J Countryman; L Gradoville; R Baumann; T Chi; M Carey
Journal:  J Virol       Date:  1993-12       Impact factor: 5.103

10.  The acidic tail of the Cdc34 ubiquitin-conjugating enzyme functions in both binding to and catalysis with ubiquitin ligase SCFCdc4.

Authors:  Gary Kleiger; Bing Hao; Dane A Mohl; Raymond J Deshaies
Journal:  J Biol Chem       Date:  2009-10-29       Impact factor: 5.157

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