Abstract
Cytidine metabolism in the yeast Saccharomyces cerevisiae was analyzed by genetic and biochemical approaches. Disruption of a unique ORF (Genbank accession No. U 20865) bearing homology with eucaryotic or bacterial cytidine deaminases abolished cytidine deaminase activity and resulted in 5-fluorocytidine resistance. The gene encoding cytidine deaminase will be referred to as CDD1 (Genbank accession number AF080089). The ability to isolate mutants resistant to 5-fluorocytidine which mapped to five other loci demonstrated the existence of a complex cytidine metabolic network. Deciphering this network revealed several original features:
(1) cytidine entry is mediated by the purine-cytosine transporter (Fcy2p),
(2) cytidine is cleaved into cytosine by the uridine nucleosidase (Urh1p),
(3) cytidine is phosphorylated into CMP by the uridine kinase (Urk1p),
(4) a block in cytosine deaminase (Fcy1p), but not in cytidine deaminase (Cdd1p), constitutes a limiting step in cytidine utilisation as a UMP precursor.
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Received: 21 November 1998/14 April 1999
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Kurtz, J., Exinger, F., Erbs, P. et al. New insights into the pyrimidine salvage pathway of Saccharomyces cerevisiae: requirement of six genes for cytidine metabolism. Curr Genet 36, 130–136 (1999). https://doi.org/10.1007/s002940050482
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DOI: https://doi.org/10.1007/s002940050482