BAIT

VMA13

CLS11, H(+)-transporting V1 sector ATPase subunit H, L000002465, YPR036W
Subunit H of the V1 peripheral membrane domain of V-ATPase; part of the electrogenic proton pump found throughout the endomembrane system; serves as an activator or a structural stabilizer of the V-ATPase; the V1 peripheral membrane domain of the vacuolar H+-ATPase (V-ATPase) has eight subunits
GO Process (1)
GO Function (1)
GO Component (3)
Saccharomyces cerevisiae (S288c)
PREY

MSN1

FUP1, HRB382, MSS10, PHD2, L000001197, YOL116W
Transcriptional activator; involved in regulation of invertase and glucoamylase expression, invasive growth and pseudohyphal differentiation, iron uptake, chromium accumulation, and response to osmotic stress; localizes to the nucleus; relative distribution to the nucleus increases upon DNA replication stress
Saccharomyces cerevisiae (S288c)

Synthetic Haploinsufficiency

A genetic interaction is inferred when mutations or deletions in separate genes, at least one of which is hemizygous, cause a minimal phenotype alone but result in lethality when combined in the same cell under a given condition.

Publication

The V-ATPase works in parallel with the HOG pathway to adapt yeast cells to osmotic stress.

Li SC, Diakov TT, Rizzo JM, Kane PM

Hyperosmotic stress activates an array of cellular detoxification mechanisms, including the high osmolarity glycerol (HOG) pathway. We report that vacuolar H(+)-ATPase (V-ATPase) activity helps provide osmotic tolerance in yeast. V-ATPase subunit genes exhibit complex haploinsufficiency interactions with HOG pathway components. vma mutants lacking V-ATPase function are sensitive to high concentrations of salt and exhibit Hog1p activation even at low salt ... [more]

Unknown Dec. 30, 2011; 0(0); [Pubmed: 22210831]

Throughput

  • Low Throughput

Ontology Terms

  • vegetative growth (APO:0000106)

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
VMA13 MSN1
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-0.4244BioGRID
2194879

Curated By

  • BioGRID