Genetic mapping of nuclear mucidin resistance mutations in Saccharomyces cerevisiae |
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Authors: | Július Šubik Stanislaw Ulaszewski André Goffeau |
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Affiliation: | (1) Food Research Institute, 82509 Bratislava, Czechoslovakia;(2) Laboratoire d'Enzymologie, Université de Louvain, 1348 Louvain-la-Neuve, Belgium;(3) Present address: Institute of Microbiology, Wroclaw University, Przybyszewskiego 63/77, 51-148 Wroclaw, Poland |
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Abstract: | Summary In the yeast Saccharomyces cerevisiae, two nuclear pleiotropic drug resistance mutations pdr3-1 (former designation mucPR) and pdr3-2 (former designation DRI9/T7) have been selected as resistant to mucidin and as resistant to chloramphenicol plus cycloheximide, respectively. The pdr3 mutations were found not to affect the plasma membrane ATPase activity measured in a crude membrane fraction. Meiotic mapping using strains with standard genetic markers revealed that mutation pdr3-1 is centromere linked on the left arm of chromosome II at a distance of 5.9 ± 3.3 cM from its centromere and 11.6 ± 3.1 cM from the marker pet9. The centromere linked pdr3-2 mutation exhibited also genetic linkage to pet9 with a map distance of 9.8 ± 3.2 cM. These results indicate that pdr3-1 and pdr3-2 are alleles of the same pleiotropic drug resistance locus PDR3 which is involved in the control of the plasma membrane permeability in yeast. |
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Keywords: | Multiple drug resistance Genetic mapping Saccharomyces cerevisiae |
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