Abstract
Repression of gene transcription is a fundamental property of nuclear hormone receptors. We report here that cell-specific repression by nuclear receptors correlates with levels of nuclear receptor corepressor (N-CoR) protein. N-CoR protein levels are regulated by mSiah2, a mammalian homolog of Drosophila Seven in absentia that targets N-CoR for proteasomal degradation. mSiah2 expression is cell-type specific and differentially regulates the repressive activities of nuclear receptors. These findings establish targeted proteolysis of transcriptional coregulators as a mechanism for cell-specific regulation of gene transcription.
Publication types
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Cell Line, Transformed
-
Cysteine Endopeptidases / metabolism*
-
Drosophila / chemistry
-
Eukaryotic Cells / cytology
-
Eukaryotic Cells / metabolism
-
Gene Expression Regulation
-
Humans
-
Hydrolysis
-
Multienzyme Complexes / metabolism*
-
Nuclear Proteins / chemistry
-
Nuclear Proteins / genetics
-
Nuclear Proteins / metabolism*
-
Nuclear Proteins / physiology
-
Nuclear Receptor Co-Repressor 1
-
Proteasome Endopeptidase Complex
-
Recombinant Proteins / genetics
-
Repressor Proteins / chemistry
-
Repressor Proteins / genetics
-
Repressor Proteins / metabolism*
-
Repressor Proteins / physiology
-
Trans-Activators / genetics
-
Trans-Activators / physiology
-
Transcription, Genetic / genetics
-
Transcriptional Activation
-
Ubiquitin-Protein Ligases
Substances
-
Multienzyme Complexes
-
NCOR1 protein, human
-
Nuclear Proteins
-
Nuclear Receptor Co-Repressor 1
-
Recombinant Proteins
-
Repressor Proteins
-
Trans-Activators
-
Ubiquitin-Protein Ligases
-
seven in absentia proteins
-
Cysteine Endopeptidases
-
Proteasome Endopeptidase Complex