Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractFunctional expression of P-glycoprotein encoded by the mouse mdr3 gene in yeast cells    Next Abstract"Functional interactions between synthetic alkyl phospholipids and the ABC transporters P-glycoprotein, Ste-6, MRP, and Pgh 1" »

J Biol Chem


Title:Functional expression of the multidrug resistance-associated protein in the yeast Saccharomyces cerevisiae
Author(s):Ruetz S; Brault M; Kast C; Hemenway C; Heitman J; Grant CE; Cole SP; Deeley RG; Gros P;
Address:"Department of Biochemistry, McGill University, Montreal, Quebec, Canada"
Journal Title:J Biol Chem
Year:1996
Volume:271
Issue:8
Page Number:4154 - 4160
DOI: 10.1074/jbc.271.8.4154
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The multidrug resistance-associated protein (MRP) is a member of the ATP binding cassette superfamily of transporters which includes the mammalian P-glycoproteins (P-gp) family. In order to facilitate the biochemical and genetic analyses of MRP, we have expressed human MRP in the yeast Saccharomyces cerevisiae and have compared its functional properties to those of the mouse Mdr3 P-gp isoform. Expression of both MRP and Mdr3 in the anthracycline hypersensitive mutant VASY2563 restored cellular resistance to Adriamycin in this mutant. MRP and Mdr3 expression produced pleiotropic effects on drug resistance in this mutant, as corresponding VASY2563 transformants also acquired resistance to the anti-fungal agent FK506 and to the K+/H+ ionophore valinomycin. The appearance of increased cellular resistance to the toxic effect of Adriamycin (ADM) in MRP and Mdr3 transformants was concomitant with a reduced intracellular accumulation of [14C]ADM in spheroplasts prepared from these cells. Moreover, MRP and Mdr3, but not control spheroplasts, could mediate a time-dependent reduction in the overall cell-associated [14C]ADM from preloaded cells, suggesting the presence of an active ADM transport mechanism in MRP and Mdr3 transformants. Finally, human MRP was found to complement the biological activity of the yeast peptide pheromone transporter Ste6 and partially restored mating in a sterile ste6 null mutant. These findings suggest that despite their relatively low level of structural homology, MRP and P-gp share similar functional aspects, since both proteins can mediate transport of chemotherapeutic drugs and the a mating peptide pheromone in yeast"
Keywords:"*ATP Binding Cassette Transporter, Subfamily B ATP Binding Cassette Transporter, Subfamily B, Member 1/*biosynthesis ATP-Binding Cassette Transporters/*biosynthesis Animals Doxorubicin/*metabolism Drug Resistance, Multiple Genetic Complementation Test Kin;"
Notes:"MedlineRuetz, S Brault, M Kast, C Hemenway, C Heitman, J Grant, C E Cole, S P Deeley, R G Gros, P eng Comparative Study Research Support, Non-U.S. Gov't Retracted Publication 1996/02/23 J Biol Chem. 1996 Feb 23; 271(8):4154-60. doi: 10.1074/jbc.271.8.4154"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024