BAIT

VOA1

YGR106C
ER protein that functions in assembly of the V0 sector of V-ATPase; functions with other assembly factors; null mutation enhances the vacuolar ATPase (V-ATPase) deficiency of a vma21 mutant impaired in endoplasmic reticulum (ER) retrieval
GO Process (1)
GO Function (0)
GO Component (2)

Gene Ontology Biological Process

Saccharomyces cerevisiae (S288c)
PREY

VHS2

YIL135C
Regulator of septin dynamics; involved in the regulation of septin dynamics at bud neck after mitotic entry, likely by stabilizing septin structure; regulated at post-translational level by cell cycle dependent phosphorylation; likely phosphorylated by Cdc28p and dephosphorylated by Cdc14p before cytokinesis; high-copy suppressor of synthetic lethality of sis2 sit4 double mutant; VHS2 has a paralog, MLF3, that arose from the whole genome duplication
GO Process (1)
GO Function (0)
GO Component (1)

Gene Ontology Biological Process

Gene Ontology Cellular Component

Saccharomyces cerevisiae (S288c)

Synthetic Growth Defect

A genetic interaction is inferred when mutations in separate genes, each of which alone causes a minimal phenotype, result in a significant growth defect under a given condition when combined in the same cell.

Publication

A Genome-wide Enhancer Screen Implicates Sphingolipid Composition in Vacuolar ATPase Function in Saccharomyces cerevisiae.

Finnigan GC, Ryan M, Stevens TH

The function of the vacuolar H(+)-ATPase enzyme complex is to acidify organelles; this process is critical for a variety of cellular processes and has implications in human disease. There are five accessory proteins that assist in assembly of the membrane portion of the complex, the V(0) domain. To identify additional elements that affect V-ATPase assembly, trafficking, or enzyme activity, we ... [more]

Unknown Dec. 31, 2010; 0(0); [Pubmed: 21196517]

Throughput

  • High Throughput

Ontology Terms

  • vegetative growth (APO:0000106)
  • metal resistance (APO:0000090)

Additional Notes

  • A synthetic genetic array (SGA) screen was used to identify genes that caused an increase in calcium or zinc sensitivity in a vma21QQ voa1::Nat-R double mutant. VOA1 is genetically linked to the VMA21 locus. The vma21QQ mutant has a dysfunctional ER retrieval motif and complete deletion of VOA1 (voa1::Nat-R) results in a decrease in steady-state levels of Vma21p.

Curated By

  • BioGRID