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PLANT PHYSIOLOGY , Vol 110, Issue 2 511-520, Copyright © 1996 by American Society of Plant Biologists
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CELL BIOLOGY AND SIGNAL TRANSDUCTION |
Molecular Cloning, Immunochemical Localization to the Vacuole, and Expression in Transgenic Yeast and Tobacco of a Putative Sugar Transporter from Sugar Beet
T. J. Chiou and D. R. Bush
Photosynthesis Research Unit, United States Department of Agriculture-Agricultural Research Service (D.R.B.), and Department of Plant Biology (T.-J.C., D.R.B.), 196 Edward R. Madigan Laboratories, 1201 West Gregory, University of Illinois, Urbana, Illinois 61801
Several plant genes have been cloned that encode members of the sugar
transporter subgroup of the major facilitator superfamily of transporters.
Here we report the cloning, expression, and membrane localization of one of
these porters found in sugar beet (Beta vulgaris L.). This clone, cDNA-1,
codes for a protein with 490 amino acids and an estimated molecular mass of
54 kD. The predicted membrane topology and sequence homology suggest that
cDNA-1 is a member of the sugar transporter family. RNA gel blot analysis
revealed that this putative sugar transporter is expressed in all
vegetative tissues and expression increases with development in leaves. DNA
gel blot analysis indicated that multiple gene copies exist for this
putative sugar transporter in the sugar beet genome. Antibodies directed
against small peptides representing the N- and C-terminal domains of the
cDNA1 protein identified a 40-kD polypeptide in microsomes isolated from
cDNA-1-transformed yeast (Saccharomyces cerevisiae). Moreover, the same
protein was identified in sugar beet and transgenic tobacco (Nicotiana
tobacum L.) membrane fractions. Detailed analysis of the transporter's
distribution across linear sucrose gradients and flotation centrifugations
showed that it co-migrates with tonoplast membrane markers. We conclude
that this carrier is located on the tonoplast membrane and that it may
mediate sugar partitioning between the vacuole and cytoplasmic
compartments.
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