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J Biol Chem, Vol. 275, Issue 19, 14217-14222, May 12, 2000
From the Department of Biochemistry, University of Bath,
Bath BA2 7AY, United Kingdom
The African trypanosome Trypanosoma
brucei has a digenetic life cycle that involves the insect vector
and the mammalian host. This is underscored by biochemical switches in
its nutritional requirements. In the insect vector, the parasite relies
on amino acid catabolism, but in the mammalian host, it derives its
energy exclusively from blood glucose. Glucose transport is
facilitated, and constitutes the rate-limiting step in ATP synthesis.
Here, we report the cloning of a novel glucose transporter-related gene by heterologous screening of a The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AJ012572.
Complementation of a Glucose Transporter Mutant of
Schizosaccharomyces pombe by a Novel Trypanosoma
brucei Gene*
,
EMBL4 genomic library of T. brucei EATRO 164 using a rat liver glucose transporter cDNA
clone. Genomic analysis shows that the gene is present as a single copy
within the parasite genome. The gene encodes a protein with an
estimated molecular mass of 55.9 kDa, which shares only segmental
homology with members of the glucose transporter superfamily.
Several potential post-translational modification sites including
phosphorylation, N-glycosylation, and
cotranslational myristoylation sites also punctuate the
sequence. It is distinguished from classical transporter proteins by
the absence of putative hydrophobic membrane-spanning domains. However,
this protein was capable of complementing Schizosaccharomyces pombe glucose transporter mutants. The rescued phenotype
conferred the ability of the cells to grow on a broad range of sugars,
both monosaccharides and disaccharides. The kinetics of glucose uptake reflected those in T. brucei. In addition to
complementation in yeast, we also showed that the gene enhanced glucose
uptake in cultured mammalian cells.
*
This work was supported in part by the Wellcome Trust.The costs of publication of this
article were defrayed in part by the payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
Recipient of a scholarship from the Sir Harold Hyam Wingate
Foundation. To whom correspondence should be addressed: Dept. of
Biochemistry and Molecular Biology, Royal Free and University College
Medical School, Rowland Hill St., London NW3 2PF, United Kingdom. Tel.:
44 207 794 0500 (ext. 4941); Fax: 44 207 794 9645; E-mail:
h.bayele@rfc.ucl.ac.uk.
§
Present address: Dept. of Haematology, King's College Hospital,
London SE5 9RS, United Kingdom.
This article has been cited by other articles:
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J. Fang, M. Sullivan, and T. F. McCutchan The Effects of Glucose Concentration on the Reciprocal Regulation of rRNA Promoters in Plasmodium falciparum J. Biol. Chem., January 2, 2004; 279(1): 720 - 725. [Abstract] [Full Text] [PDF] |
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