Abstract
The general transcriptional repressor Tup1p requires the cyclin/cyclin-dependent kinase pair Srb11p/Srb10p in the holoenzyme of transcription. We used the split-ubiquitin system to demonstrate that Tup1p interacts with Srb11p in vivo. We confirmed our observation in vitro with the help of purified proteins, and we compared the de-repression effect of deleting TUP1, SRB10, and SRB11 on different promoters. We propose that Tup1p targets the cyclin Srb11p to affect the cyclin-dependent kinase Srb10p.
Copyright 2003 S. Karger AG, Basel
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Cyclin-Dependent Kinase 8
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Cyclin-Dependent Kinases / genetics
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Cyclin-Dependent Kinases / metabolism
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Cyclins / metabolism*
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DNA-Directed RNA Polymerases / metabolism*
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Nuclear Proteins / genetics*
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Nuclear Proteins / metabolism
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Promoter Regions, Genetic
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Protein Binding
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Repressor Proteins / genetics*
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Repressor Proteins / metabolism
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Saccharomyces cerevisiae / genetics*
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Saccharomyces cerevisiae Proteins / genetics*
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Saccharomyces cerevisiae Proteins / metabolism
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Transcription Factors
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Transcription, Genetic
Substances
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Cyclins
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Nuclear Proteins
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Repressor Proteins
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Saccharomyces cerevisiae Proteins
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TUP1 protein, S cerevisiae
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Transcription Factors
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SSN8 protein, S cerevisiae
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Cyclin-Dependent Kinase 8
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Cyclin-Dependent Kinases
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SSN3 protein, S cerevisiae
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DNA-Directed RNA Polymerases