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Catic, André; Suh, Carol Y.; Hill, Cedric T.; Daheron, Laurence; Henkel, Theresa; Orford, Keith W.; Dombkowski, David M.; Liu, Tao; Liu, X. Shirley; Scadden, David T.
Cell, 12/2013, Letnik: 155, Številka: 6Journal Article
Transcription factor activity and turnover are functionally linked, but the global patterns by which DNA-bound regulators are eliminated remain poorly understood. We established an assay to define the chromosomal location of DNA-associated proteins that are slated for degradation by the ubiquitin-proteasome system. The genome-wide map described here ties proteolysis in mammalian cells to active enhancers and to promoters of specific gene families. Nuclear-encoded mitochondrial genes in particular correlate with protein elimination, which positively affects their transcription. We show that the nuclear receptor corepressor NCoR1 is a key target of proteolysis and physically interacts with the transcription factor CREB. Proteasome inhibition stabilizes NCoR1 in a site-specific manner and restrains mitochondrial activity by repressing CREB-sensitive genes. In conclusion, this functional map of nuclear proteolysis links chromatin architecture with local protein stability and identifies proteolytic derepression as highly dynamic in regulating the transcription of genes involved in energy metabolism. Display omitted •An activity-based assay localizes degradation of DNA-bound proteins•Proteolysis is dominant at enhancers and at promoters of distinct gene ontologies•Steady expression of mitochondrial genes requires degradation of NCoR1•Ubiquitin ligase Siah2 mediates derepression especially at CREB target promoters A genome-wide proteolysis map shows a correlation between DNA-bound protein degradation and active gene promoters. In particular, continual removal of the corepressor NCoR1 from nuclear-encoded mitochondrial genes is required for optimal mitochondrial function.
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