Analysis of the in vivo interaction between a basic repressor and an acidic activator

The artificial basic repressor SSB24 represses transcription of a reporter construct activated by GCN4. We show that the positively charged SSB24 and the negatively charged acidic activator GCN4 interact in vitro and in vivo. However, deleting the interaction domain from the GCN4 activator does not...

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Veröffentlicht in:FEBS letters 1999-06, Vol.453 (3), p.299-304
Hauptverfasser: Wellhausen, Anne, Lehming, Norbert
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Lehming, Norbert
description The artificial basic repressor SSB24 represses transcription of a reporter construct activated by GCN4. We show that the positively charged SSB24 and the negatively charged acidic activator GCN4 interact in vitro and in vivo. However, deleting the interaction domain from the GCN4 activator does not result in loss of repression by SSB24. Similarly, transcription activated by the holoenzyme component SRB2 is repressed, although SSB24 and SRB2 do not interact. Repression by SSB24 therefore does not depend on the observed protein-protein interaction between SSB24 and GCN4.
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subjects Acids - metabolism
Alkalies - metabolism
DNA Mutational Analysis
DNA-Binding Proteins
Fungal Proteins - metabolism
GCN4
Gene Expression Regulation
Mediator Complex
Protein Binding
Protein Kinases - metabolism
Recombinant Proteins
Repression
Repressor Proteins - metabolism
Saccharomyces cerevisiae Proteins
Sequence Deletion
Split ubiquitin assay
SSB24
Trans-Activators - metabolism
Transcription Factors - metabolism
Ubiquitins - metabolism
title Analysis of the in vivo interaction between a basic repressor and an acidic activator
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