Functional production of mammalian concentrative nucleoside transporters in Saccharomyces cerevisiae |
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Authors: | Mark F. Vickers James D. Young Stephen A. Baldwin Michael J. Ellison Carol E. Cass |
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Affiliation: | 1. University of Alberta, Edmonton, Alberta, Canada and Cross Cancer Institute, 11560 University Avenue, Edmonton, Alberta, TG6 1Z2, Canada;2. University of Alberta, Edmonton, Alberta, Canada;3. School of Biochemistry and Molecular Biology, University of Leeds, Leeds, UK |
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Abstract: | The transport of nucleosides and nucleobases in the yeast Saccharomyces cerevisiae is reviewed and the use of this organism to study recombinant mammalian concentrative nucleoside transport (CNT) proteins is described. A selection strategy based on the ability of an expressed nucleoside transporter cDNA to mediate thymidine uptake by yeast under a selective condition that depletes endogenous thymidylate was used to assess the transport capacity of heterologous transporter proteins. The pyrimidine-nucleoside selective concentrative transporters from human (hCNT1) and rat (rCNT1) complemented the imposed thymidylate depletion in S. cerevisiae, as did N-terminally truncated versions of hCNT1 and rCNT1 lacking up to 31 amino acids. Transporter-mediated rescue of S. cerevisiae by both nucleoside transporters was inhibited by cytidine, uridine and adenosine, but not by guanosine or inosine. This work represents the development of a new model system for the functional production of recombinant nucleoside transporters of the CNT family of membrane proteins. |
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Keywords: | Nucleoside Transport Cerevisiae Heterologous Expression |
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