BAIT

BPH1

L000003507, YCR032W
Protein homologous to Chediak-Higashi syndrome and Beige proteins; both of which are implicated in disease syndromes in human and mouse, respectively, due to defective lysosomal trafficking; mutant phenotype and genetic interactions suggest a role in protein sorting
GO Process (3)
GO Function (0)
GO Component (3)
Saccharomyces cerevisiae (S288c)
PREY

FLO1

FLO2, FLO4, flocculin FLO1, L000000617, L000000616, YAR050W
Lectin-like protein involved in flocculation; cell wall protein that binds mannose chains on the surface of other cells, confers floc-forming ability that is chymotrypsin sensitive and heat resistant; FLO1 has a paralog, FLO5, that arose from a segmental duplication
GO Process (5)
GO Function (1)
GO Component (1)
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

Bph1p, the Saccharomyces cerevisiae homologue of CHS1/beige, functions in cell wall formation and protein sorting.

Shiflett SL, Vaughn MB, Huynh D, Kaplan J, Ward DM

Mutations in the Chediak-Higashi syndrome gene (CHS1) and its murine homologue Beige result in the formation of enlarged lysosomes. BPH1 (Beige Protein Homologue 1) encodes the Saccharomyces cerevisiae homologue of CHS1/Beige. BPH1 is not essential and the encoded protein was found to be both cytosolic and peripherally bound to a membrane. Neither disruption nor overexpression of BPH1 affected vacuole morphology ... [more]

Traffic Sep. 01, 2004; 5(9);700-10 [Pubmed: 15296494]

Throughput

  • Low Throughput

Ontology Terms

  • phenotype: resistance to chemicals (APO:0000087)
  • phenotype: acid ph resistance (APO:0000201)

Additional Notes

  • High copy suppressors of the growth defect of bph1 on both low pH potassium acetate and calcofluor white

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
FLO1 BPH1
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-3.1736BioGRID
895937

Curated By

  • BioGRID