This Article Full Text Full Text (PDF) Other Versions of this Article: EC.00290-06v1 6/2/134    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Vargas, R. C. Articles by Sá-Correia, I. Search for Related Content PubMed PubMed Citation Articles by Vargas, R. C. Articles by Sá-Correia, I.

Saccharomyces cerevisiae Multidrug Resistance Transporter Qdr2 Is Implicated in Potassium Uptake, Providing a Physiological Advantage to Quinidine-Stressed Cells

IBB-Institute for Biotechnology and Bioengineering, Centre for Biological and Chemical Engineering, Instituto Superior Técnico. Av. Rovisco Pais, 1049-001 Lisboa, Portugal,¹ Departamento de Microbiología, Universidad de Córdoba, Edificio Severo Ochoa, Campus de Rabanales, 14071 Córdoba, Spain²

Received 7 September 2006/ Accepted 13 December 2006

The QDR2 gene of Saccharomyces cerevisiae encodes a putative plasma membrane drug:H⁺ antiporter that confers resistance against quinidine, barban, bleomycin, and cisplatin. This work provides experimental evidence of defective K⁺ (Rb⁺) uptake in the absence of QDR2. The direct involvement of Qdr2p in K⁺ uptake is reinforced by the fact that increased K⁺ (Rb⁺) uptake due to QDR2 expression is independent of the Trk1p/Trk2p system. QDR2 expression confers a physiological advantage for the yeast cell during the onset of K⁺ limited growth, due either to a limiting level of K⁺ in the growth medium or to the presence of quinidine. This drug decreases the K⁺ uptake rate and K⁺ accumulation in the yeast cell, especially in the qdr2 mutant. Qdr2p also helps to sustain the decrease of intracellular pH in quinidine-stressed cells in growth medium at pH 5.5 by indirectly promoting H⁺ extrusion affected by the drug. The results are consistent with the hypothesis that Qdr2p may also couple K⁺ movement with substrate export, presumably with quinidine. Other clues to the biological role of QDR2 in the yeast cell come from two additional lines of experimental evidence. First, QDR2 transcription is activated under nitrogen (NH₄⁺) limitation or when the auxotrophic strain examined enters stationary phase due to leucine limitation, this regulation being dependent on general amino acid control by Gcn4p. Second, the amino acid pool is higher in qdr2 cells than in wild-type cells, indicating that QDR2 expression is, directly or indirectly, involved in amino acid homeostasis.

Published ahead of print on 22 December 2006.