BAIT

PDR1

AMY1, ANT1, BOR2, CYH3, NRA2, SMR2, TIL1, TPE1, TPE3, drug-responsive transcription factor PDR1, L000002984, L000003503, L000001361, YGL013C
Transcription factor that regulates the pleiotropic drug response; zinc cluster protein that is a master regulator involved in recruiting other zinc cluster proteins to pleiotropic drug response elements (PDREs) to fine tune the regulation of multidrug resistance genes; relocalizes to the cytosol in response to hypoxia; PDR1 has a paralog, PDR3, that arose from the whole genome duplication
Saccharomyces cerevisiae (S288c)
PREY

DEP1

FUN54, Rpd3L histone deacetylase complex subunit DEP1, L000000502, YAL013W
Component of the Rpd3L histone deacetylase complex; required for diauxic shift-induced histone H2B deposition onto rDNA genes; transcriptional modulator involved in regulation of structural phospholipid biosynthesis genes and metabolically unrelated genes, as well as maintenance of telomeres, mating efficiency, and sporulation
GO Process (15)
GO Function (0)
GO Component (2)

Gene Ontology Cellular Component

Saccharomyces cerevisiae (S288c)

Phenotypic Enhancement

A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.

Publication

Networks of genes modulating the pleiotropic drug response in Saccharomyces cerevisiae.

Yibmantasiri P, Bircham PW, Maass DR, Bellows DS, Atkinson PH

The pleiotropic drug response (PDR) or multidrug resistance (MDR) are cellular defence mechanisms present in all species to deal with potential toxicity from environmental small molecule toxins or bioactives. The rapid induction of MDR by xenobiotics in mammalian cells and PDR in budding yeast (S. cerevisiae) has been well studied but how pathway specificity is achieved across different structural classes ... [more]

Mol Biosyst Nov. 08, 2013; 0(0); [Pubmed: 24201294]

Throughput

  • Low Throughput

Ontology Terms

  • phenotype: resistance to chemicals (APO:0000087)

Additional Notes

  • pdr1 pdr3 dep1 triple mutants showed increased sensitivity to compounds over that showed by pdr1 pdr3 double mutants, implying the existence of PDR mechanisms outside of the PDR1 PDR3 route

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
DEP1 PDR1
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-0.1556BioGRID
354922
PDR1 DEP1
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-0.1556BioGRID
381306

Curated By

  • BioGRID