BAIT

AVL9

S000029049, S000029007, YLR114C
Conserved protein involved in exocytic transport from the Golgi; mutation is synthetically lethal with apl2 vps1 double mutation; member of a protein superfamily with orthologs in diverse organisms; relocalizes from bud neck to cytoplasm upon DNA replication stress
GO Process (1)
GO Function (0)
GO Component (2)

Gene Ontology Biological Process

Gene Ontology Cellular Component

Saccharomyces cerevisiae (S288c)
PREY

SEC4

SRO6, Rab family GTPase SEC4, L000001830, YFL005W
Rab family GTPase; essential for vesicle-mediated exocytic secretion and autophagy; associates with the exocyst component Sec15p and may regulate polarized delivery of transport vesicles to the exocyst at the plasma membrane
Saccharomyces cerevisiae (S288c)

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 synaptobrevin homologue Snc2p recruits the exocyst to secretory vesicles by binding to Sec6p.

Shen D, Yuan H, Hutagalung A, Verma A, Kuemmel D, Wu X, Reinisch K, McNew JA, Novick P

A screen for mutations that affect the recruitment of the exocyst to secretory vesicles identified genes encoding clathrin and proteins that associate or colocalize with clathrin at sites of endocytosis. However, no significant colocalization of the exocyst with clathrin was seen, arguing against a direct role in exocyst recruitment. Rather, these components are needed to recycle the exocytic vesicle SNAREs ... [more]

J. Cell Biol. Aug. 05, 2013; 202(3);509-26 [Pubmed: 23897890]

Throughput

  • Low Throughput

Ontology Terms

  • phenotype: protein/peptide distribution (APO:0000209)

Additional Notes

  • exocyst (sec15) localization

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
AVL9 SEC4
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-11.3423BioGRID
894778

Curated By

  • BioGRID