BAIT

RPT2

YHS4, YTA5, proteasome regulatory particle base subunit RPT2, L000002559, YDL007W
ATPase of the 19S regulatory particle of the 26S proteasome; one of six ATPases of the regulatory particle; involved in the degradation of ubiquitinated substrates; required for normal peptide hydrolysis by the core 20S particle; N-myristoylation of Rpt2p at Gly2 is involved in regulating the proper intracellular distribution of proteasome activity by controlling the nuclear localization of the 26S proteasome
Saccharomyces cerevisiae (S288c)
PREY

RNY1

YPL123C
Vacuolar RNase of the T(2) family; relocalizes to the cytosol where it cleaves tRNAs upon oxidative or stationary phase stress; promotes apoptosis under stress conditions and this function is independent of its catalytic activity
GO Process (3)
GO Function (1)
GO Component (4)

Gene Ontology Molecular Function

Gene Ontology Cellular Component

Saccharomyces cerevisiae (S288c)

Dosage Rescue

A genetic interaction is inferred when over expression or increased dosage of one gene rescues the lethality or growth defect of a strain that is mutated or deleted for another gene.

Publication

Yeast Nst1 is a novel component of P-bodies and is a specific suppressor of proteasome base assembly defects.

Cheng CL, Wong MK, Hochstrasser M

Proteasome assembly utilizes multiple dedicated assembly chaperones and is regulated by signaling pathways that respond to diverse stress conditions. To discover new factors influencing proteasome base assembly, we screened a tiled high-copy yeast genomic library to identify dosage suppressors of a temperature-sensitive proteasome regulatory particle (RP) base mutant. The screen identified negative salt tolerance 1 (Nst1), a protein that when ... [more]

Mol Biol Cell Oct. 01, 2021; 32(20);ar6 [Pubmed: 34347506]

Throughput

  • High Throughput

Ontology Terms

  • phenotype: temperature sensitive growth (APO:0000092)

Additional Notes

  • suppression of the strong RPT2,5 PA growth defect at elevated temperature

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
RNY1 RPT2
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-0.1274BioGRID
2073005

Curated By

  • BioGRID