ENC
Gene Ontology Biological Process
- cystoblast division [IMP, TAS]
- germ-line cyst formation [TAS]
- germarium-derived egg chamber formation [IMP]
- germarium-derived oocyte fate determination [IMP, TAS]
- karyosome formation [TAS]
- mitotic nuclear division [TAS]
- oocyte axis specification [TAS]
- oocyte dorsal/ventral axis specification [TAS]
- oogenesis [IMP, TAS]
- regulation of pole plasm oskar mRNA localization [TAS]
CYCE
Gene Ontology Biological Process
- G1/S transition of mitotic cell cycle [IDA, IMP, TAS]
- JAK-STAT cascade [IGI]
- cell adhesion [IMP]
- cell proliferation involved in compound eye morphogenesis [IMP]
- cellular process [IMP]
- cellular response to DNA damage stimulus [IMP]
- eggshell chorion gene amplification [IMP]
- mitotic cell cycle [IMP]
- negative regulation of mitotic anaphase-promoting complex activity [IGI]
- neuroblast fate determination [IMP]
- neuron fate specification [IDA]
- oogenesis [TAS]
- peripheral nervous system development [IEP, TAS]
- pole cell development [IEP]
- positive regulation of G1/S transition of mitotic cell cycle [IMP]
- positive regulation of apoptotic process [IMP]
- regulation of DNA replication [IMP]
- regulation of cell proliferation [IMP]
- regulation of cell shape [IMP]
- regulation of exit from mitosis [IGI]
- regulation of imaginal disc-derived wing size [IMP]
- regulation of protein phosphorylation [IDA]
- sensory organ development [NAS]
- sensory organ precursor cell division [IMP]
- somatic stem cell maintenance [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-Western
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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.
Publication
Encore facilitates SCF-Ubiquitin-proteasome-dependent proteolysis during Drosophila oogenesis.
Exit from the cell cycle requires the downregulation of Cyclin/Cdk activity. In the ovary of Drosophila, Encore activity is necessary in the germline to exit the division program after four mitotic divisions. We find that in encore mutant germaria, Cyclin A persists longer than in wild type. In addition, Cyclin E expression is not downregulated after the fourth mitosis and ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| CYCE ENC | Affinity Capture-Western Affinity Capture-Western 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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - | |
| ENC CYCE | Phenotypic Suppression 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. | Low | - | FlyBase | - |
Curated By
- BioGRID