CLN1
Gene Ontology Biological Process
Gene Ontology Molecular Function
BUD2
Gene Ontology Biological Process
- axial cellular bud site selection [IMP]
- bipolar cellular bud site selection [IMP]
- establishment or maintenance of cell polarity [IMP]
- filamentous growth [IMP]
- invasive filamentous growth [IMP]
- mitotic spindle orientation checkpoint [IMP]
- negative regulation of Ras protein signal transduction [IBA]
- positive regulation of Ras GTPase activity [IBA]
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
Yeast G1 cyclins CLN1 and CLN2 and a GAP-like protein have a role in bud formation.
Cyclin-dependent protein kinases have a central role in cell cycle regulation. In Saccharomyces cerevisiae, Cdc28 kinase and the G1 cyclins Cln1, 2 and 3 are required for DNA replication, duplication of the spindle pole body and bud emergence. These three independent processes occur simultaneously in late G1 when the cells reach a critical size, an event known as Start. At ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Additional Notes
- cln1 cln2 double mutant background
- genetic complex
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
CLN1 BUD2 | 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 | -0.6932 | BioGRID | 2446136 | |
CLN1 BUD2 | 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 | 352107 |
Curated By
- BioGRID