GCR1
Gene Ontology Biological Process
- negative regulation of transcription from RNA polymerase II promoter by glucose [IMP]
- nucleosome organization [IMP]
- positive regulation of ribosomal protein gene transcription from RNA polymerase II promoter [IMP]
- positive regulation of transcription from RNA polymerase II promoter [IMP]
- positive regulation of transcription from a mobile element promoter [IMP]
- regulation of glycolytic by positive regulation of transcription from RNA polymerase II promoter [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
NUP53
Gene Ontology Biological Process
- NLS-bearing protein import into nucleus [IGI, IMP]
- nuclear pore organization [IGI]
- positive regulation of transcription, DNA-templated [IDA, IGI]
- protein import into nucleus [IGI]
- protein localization to kinetochore [IMP]
- regulation of mitosis [IMP, IPI]
- regulation of protein desumoylation [IMP, IPI]
- response to spindle checkpoint signaling [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
The nuclear pore complex mediates binding of the mig1 repressor to target promoters.
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccharomyces cerevisiae, the best-studied downstream effector of this response is the glucose-regulated repressor Mig1. We show here that nuclear pore complexes also contribute to glucose-regulated gene expression. NPCs participate in glucose-responsive repression by physically interacting with Mig1 and mediating its function independently of nucleocytoplasmic transport. Surprisingly, ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: protein/peptide accumulation (APO:0000149)
Additional Notes
- deletion of nup42 or nup53 partially suppresses the defect in Suc2 regulation caused by deletion of Gcr1
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| GCR1 NUP53 | 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 | 166918 |
Curated By
- BioGRID