EAF1
Gene Ontology Biological Process
Gene Ontology Cellular Component
SWE1
Gene Ontology Biological Process
- G2 cell size control checkpoint [IEP, IMP]
- G2/M transition of mitotic cell cycle [IDA, IMP, ISS]
- cytokinesis after mitosis checkpoint [IDA, IEP, IMP]
- negative regulation of spindle pole body separation [IGI, IMP]
- protein phosphorylation [IDA]
- re-entry into mitotic cell cycle [IGI]
- regulation of cell size [IMP]
- regulation of cyclin-dependent protein serine/threonine kinase activity [IDA]
- regulation of meiosis [IEP, IGI, IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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.
Publication
Regulation of Septin Dynamics by the Saccharomyces cerevisiae Lysine Acetyltransferase NuA4.
In the budding yeast Saccharomyces cerevisiae, the lysine acetyltransferase NuA4 has been linked to a host of cellular processes through the acetylation of histone and non-histone targets. To discover proteins regulated by NuA4-dependent acetylation, we performed genome-wide synthetic dosage lethal screens to identify genes whose overexpression is toxic to non-essential NuA4 deletion mutants. The resulting genetic network identified a novel ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: heat sensitivity (APO:0000147)
- phenotype: budding (APO:0000024)
Additional Notes
- deletion of swe1 partially rescues the bud morphology defect and temperature sensitivity of an eaf1 mutant
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
EAF1 SWE1 | Dosage Lethality Dosage Lethality A genetic interaction is inferred when over expression or increased dosage of one gene causes lethality in a strain that is mutated or deleted for another gene. | Low | - | BioGRID | 567636 | |
EAF1 SWE1 | Positive Genetic Positive Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores. | High | - | BioGRID | 3530761 |
Curated By
- BioGRID