Subcellular distribution and membrane topology of the mammalian concentrative Na+-nucleoside cotransporter rCNT1

J Biol Chem. 2001 Jul 27;276(30):27981-8. doi: 10.1074/jbc.M100518200. Epub 2001 May 25.


The rat transporter rCNT1 is the archetype of a family of concentrative nucleoside transporters (CNTs) found both in eukaryotes and in prokaryotes. In the present study we have used antibodies to investigate the subcellular distribution and membrane topology of this protein. rCNT1 was found to be expressed predominantly in the brush-border membranes of the polarized epithelial cells of rat jejunum and renal cortical tubules and in the bile canalicular membranes of liver parenchymal cells, consistent with roles in the absorption of dietary nucleosides, of nucleosides in the glomerular filtrate, or of nucleosides arising from the action of extracellular nucleotidases, respectively. The effect of endoglycosidase F treatment on wild-type and mutant rCNT1 expressed in Xenopus oocytes revealed that the recombinant transporter could be glycosylated at either or both of Asn605 and Asn643, indicating that its C terminus is extracellular. In contrast, potential N-glycosylation sites introduced near the N terminus, or between putative transmembrane (TM) helices 4 and 5, were not glycosylated. The deduced orientation of the N terminus in the cytoplasm was confirmed by immunocytochemistry on intact and saponin-permeabilized Chinese hamster ovary cells expressing recombinant rCNT1. These results, in conjunction with extensive analyses of CNT family protein sequences using predictive algorithms, lead us to propose a revised topological model, in which rCNT1 possesses 13 TM helices with the hydrophilic N-terminal and C-terminal domains on the cytoplasmic and extracellular sides of the membrane, respectively. Furthermore, we show that the first three TM helices, which are absent from prokaryote CNTs, are not essential for transporter function; truncated proteins lacking these helices, derived either from rCNT1 or from its human homolog hCNT1, were found to retain significant sodium-dependent uridine transport activity when expressed in oocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Asparagine / chemistry
  • Biological Transport
  • Blotting, Western
  • CHO Cells
  • Carrier Proteins / chemistry*
  • Carrier Proteins / physiology*
  • Cell Membrane / metabolism
  • Cricetinae
  • DNA, Complementary / metabolism
  • Gene Deletion
  • Glycosylation
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa / metabolism
  • Kidney / metabolism
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase / pharmacology
  • Membrane Transport Proteins*
  • Mutagenesis, Site-Directed
  • Mutation
  • Oocytes / metabolism
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Rats
  • Recombinant Proteins / metabolism
  • Tissue Distribution
  • Transcription, Genetic
  • Transfection
  • Uridine / metabolism
  • Xenopus


  • Carrier Proteins
  • DNA, Complementary
  • Membrane Transport Proteins
  • Recombinant Proteins
  • cif nucleoside transporter
  • Asparagine
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase
  • Uridine