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
DOT1
Gene Ontology Biological Process
- DNA damage checkpoint [IGI, IMP]
- G1 DNA damage checkpoint [IMP]
- chromatin silencing at telomere [IMP]
- global genome nucleotide-excision repair [IMP]
- histone H3-K79 methylation [IDA, IMP]
- intra-S DNA damage checkpoint [IMP]
- meiotic recombination checkpoint [IGI]
- nucleotide-excision repair [IGI, IMP]
- postreplication repair [IGI]
- recombinational repair [IGI, IMP]
Gene Ontology Molecular Function
Phenotypic Suppression
A genetic interaction is inferred when mutation or over expression of one gene results in suppression of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.
Publication
Loss of Histone H3 Methylation at Lysine 4 Triggers Apoptosis in Saccharomyces cerevisiae.
Monoubiquitination of histone H2B lysine 123 regulates methylation of histone H3 lysine 4 (H3K4) and 79 (H3K79) and the lack of H2B ubiquitination in Saccharomyces cerevisiae coincides with metacaspase-dependent apoptosis. Here, we discovered that loss of H3K4 methylation due to depletion of the methyltransferase Set1p (or the two COMPASS subunits Spp1p and Bre2p, respectively) leads to enhanced cell death during ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: apoptosis (APO:0000155)
Additional Notes
- dot1 deletion suppresses apoptotic marks in set1 mutants
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| SET1 DOT1 | Phenotypic Enhancement Phenotypic Enhancement A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene. | Low | - | BioGRID | 1435407 | |
| DOT1 SET1 | Phenotypic Enhancement Phenotypic Enhancement A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene. | Low | - | BioGRID | 342650 | |
| DOT1 SET1 | Synthetic Growth Defect Synthetic Growth Defect A genetic interaction is inferred when mutations in separate genes, each of which alone causes a minimal phenotype, result in a significant growth defect under a given condition when combined in the same cell. | Low | - | BioGRID | 349858 | |
| DOT1 SET1 | Synthetic Lethality 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. | Low | - | BioGRID | 164471 | |
| SET1 DOT1 | Synthetic Rescue Synthetic Rescue A genetic interaction is inferred when mutations or deletions of one gene rescues the lethality or growth defect of a strain mutated or deleted for another gene. | Low | - | BioGRID | 927630 |
Curated By
- BioGRID