RTG2
Gene Ontology Biological Process
- maintenance of DNA trinucleotide repeats [IMP]
- mitochondria-nucleus signaling pathway [IMP]
- negative regulation of extrachromosomal rDNA circle accumulation involved in replicative cell aging [IMP]
- nitrogen catabolite regulation of transcription from RNA polymerase II promoter [IMP]
- positive regulation of transcription from RNA polymerase II promoter [IDA, IGI, IMP]
- regulation of transcription from RNA polymerase II promoter [IMP]
- transcription factor import into nucleus [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
GCN5
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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.
Publication
Interplay among Gcn5, Sch9 and mitochondria during chronological aging of wine yeast is dependent on growth conditions.
Saccharomyces cerevisiae chronological life span (CLS) is determined by a wide variety of environmental and genetic factors. Nutrient limitation without malnutrition, i.e. dietary restriction, expands CLS through the control of nutrient signaling pathways, of which TOR/Sch9 has proven to be the most relevant, particularly under nitrogen deprivation. The use of prototrophic wine yeast allows a better understanding of the role ... [more]
Throughput
- Low Throughput
Ontology Terms
- chronological lifespan (APO:0000316)
Additional Notes
- wine strains
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| GCN5 RTG2 | Affinity Capture-MS Affinity Capture-MS An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods. | High | - | BioGRID | 546005 | |
| GCN5 RTG2 | 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 | -0.2721 | BioGRID | 384331 |
Curated By
- BioGRID