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Volume 272, Number 26,
Issue of June 27, 1997
pp. 16548-16554
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Cloning and Functional Characterization of a Rat Renal Organic
Cation Transporter Isoform (rOCT1A)
(Received for publication, April 22, 1997)
Lei
Zhang
,
Mark J.
Dresser
,
Joanne K.
Chun
,
Patricia C.
Babbitt
and
Kathleen M.
Giacomini
From the Departments of Biopharmaceutical Sciences and
Pharmaceutical Chemistry, University of California,
San Francisco, California 94143
Polyspecific organic cation transporters in the
renal proximal tubule mediate the secretion of many clinically used
drugs as well as endogenous metabolites. Recently, two organic cation transporters (rOCT1 and rOCT2) were cloned from rat
kidney. In this study, we report the cloning and functional expression
of an rOCT1 isoform, rOCT1A, from rat kidney. Genomic DNA
cloning and sequencing demonstrated that rOCT1A is an
alternatively spliced variant of rOCT1 with a deletion of 104 base pairs near the 5 -end. The uptake of
[14C]tetraethylammonium (TEA) in oocytes injected
with the cRNA-encoding rOCT1A was increased 16-fold over that in
water-injected oocytes (29 ± 2.8 pmol/oocyte/h versus
1.8 ± 0.13 pmol/oocyte/h, mean ± S.E., p < 0.05). [14C]TEA uptake in the cRNA-injected oocytes
was saturable (Km = 42 ± 11 µM)
and was inhibited significantly by organic cations, including
cimetidine and N1-methylnicotinamide.
The amino acid sequence was deduced from the cDNA after examination
of all three reading frames. Two overlapping open reading frames were
found. Studies with synthetic constructs suggest that a functional
organic cation transporter is encoded by the larger open reading frame.
The larger open reading frame encodes a 430-amino acid protein (termed
rOCT1A) that is 92% identical to rOCT1 and 57%
identical to rOCT2. From hydropathy analysis, rOCT1A is
predicted to have 10 transmembrane domains with both amino and
carboxyl termini intracellular. RNase protection assays demonstrate the presence of rOCT1A mRNA transcripts in rat
kidney cortex, medulla, and intestine. These studies demonstrate the presence of a functional, alternatively spliced organic cation transporter (rOCT1A) in rat kidney.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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