Affiliation:
1. Department of Biology, Lund University, Lund, Sweden
2. Washington University, St. Louis, Missouri, USA
Abstract
ABSTRACT
Pyrimidines are important nucleic acid precursors which are constantly synthesized, degraded, and rebuilt in the cell. Four degradation pathways, two of which are found in eukaryotes, have been described. One of them, the
URC
pathway, has been initially discovered in our laboratory in the yeast
Lachancea kluyveri
. Here, we present the global changes in gene expression in
L. kluyveri
in response to different nitrogen sources, including uracil, uridine, dihydrouracil, and ammonia. The expression pattern of the known
URC
genes,
URC1-6
, helped to identify nine putative novel
URC
genes with a similar expression pattern. The microarray analysis provided evidence that both the
URC
and
PYD
genes are under nitrogen catabolite repression in
L. kluyveri
and are induced by uracil or dihydrouracil, respectively. We determined the function of
URC8
, which was found to catalyze the reduction of malonate semialdehyde to 3-hydroxypropionate, the final degradation product of the pathway. The other eight genes studied were all putative permeases. Our analysis of double deletion strains showed that the
L. kluyveri
Fui1p protein transported uridine, just like its homolog in
Saccharomyces cerevisiae
, but we demonstrated that is was not the only uridine transporter in
L. kluyveri
. We also showed that the
L. kluyveri
homologs of
DUR3
and
FUR4
do not have the same function that they have in
S. cerevisiae
, where they transport urea and uracil, respectively. In
L. kluyveri
, both of these deletion strains grew normally on uracil and urea.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
14 articles.
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