RPT6
Gene Ontology Biological Process
- chromatin remodeling [IMP]
- negative regulation of sequence-specific DNA binding transcription factor activity [IMP]
- nonfunctional rRNA decay [IMP]
- nucleotide-excision repair [IGI]
- positive regulation of RNA polymerase II transcriptional preinitiation complex assembly [IGI, IMP]
- positive regulation of sequence-specific DNA binding transcription factor activity [IMP]
- positive regulation of transcription elongation from RNA polymerase II promoter [IMP]
- proteasome regulatory particle assembly [IMP]
- proteasome-mediated ubiquitin-dependent protein catabolic process [IPI]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SET1
Gene Ontology Biological Process
- ascospore formation [IMP]
- chromatin silencing at rDNA [TAS]
- chromatin silencing at silent mating-type cassette [IMP]
- chromatin silencing at telomere [IMP]
- histone H3-K4 methylation [IDA, IMP]
- peptidyl-lysine dimethylation [IMP, IPI]
- positive regulation of histone acetylation [IGI]
- regulation of transcription from RNA polymerase II promoter in response to stress [IGI, IMP]
- telomere maintenance [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Synthetic Lethality
A genetic interaction is inferred when mutations or deletions in separate genes, each of which alone causes a minimal phenotype, result in lethality when combined in the same cell under a given condition.
Publication
Proteasomal ATPases link ubiquitylation of histone H2B to methylation of histone H3.
In Saccharomyces cerevisiae, methylation of histone H3 at active genes is an epigenetic mark that distinguishes active from silent chromatin and functions as a short-term "memory" of recent transcription. Methylation of H3 at lysine residues K4 and K79 depends on ubiquitylation of histone H2B, but the mechanisms linking H2B ubiquitylation to H3 methylation are unknown. Here, we demonstrate that proteasomal ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| SET1 RPT6 | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | High | -0.1861 | BioGRID | 2047896 |
Curated By
- BioGRID