Abstract
PEPT2 is a high-affinity H+/dipeptide transporter expressed in kidney, brain, lung, and mammary gland. The physiological role of PEPT2 in kidney is to reabsorb small peptides generated by luminal peptidases. PEPT2 is also a transporter for peptide-like drugs such as penicillins and cephalosporins. We have conducted a haplotype analysis of 27 single nucleotide polymorphisms located in or near exons of the human gene encoding hPEPT2 (SLC15A2), using genotyping data from 247 genomic DNA samples from the Coriell collection. Our analysis reveals that hPEPT2 has a >6-kilobase sequence block with at least 10 abundant polymorphisms in almost complete linkage disequilibrium. As a result, only two main hPEPT2 variants exist (hPEPT2*1 and *2) with several phased amino acid substitutions, present in substantial frequencies in all ethnic groups tested. When expressed in Chinese hamster ovary cells, hPEPT2*1 and *2 displayed similar Vmax values for glycyl-sarcosine (Gly-Sar), but they differed significantly in their Km values (83 ± 16 and 233 ± 38 μM, respectively). Moreover, hPEPT2*1 and *2 differed in their pH sensitivity for H+/Gly-Sar transport. In addition, hPEPT2*1 and *2 generated varying levels of mRNA in nine heterozygous kidney tissue samples, including one allele expressing no detectable mRNA, suggesting the presence of cis-acting polymorphisms affecting transcription or mRNA processing. The results indicate that polymorphisms in the gene encoding hPEPT2 can alter substrate transport and therefore could affect drug disposition in vivo.
Footnotes
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This work was in part supported by the University of California, San Francisco, Plasma Membrane Transporter Group (Grant GM61390 from General Medical Sciences, National Institutes of Health), by funds from The Ohio State University, and The Carlsberg Foundation (to C.U.N.).
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doi:10.1124/jpet.104.073098.
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ABBREVIATIONS: Gly-Sar, glycyl-sarcosine; SNP, single nucleotide polymorphism; kb, kilobase; PCR, polymerase chain reaction; HPLC, high-pressure liquid chromatography; CHO, Chinese hamster ovary; MES, 2-(N-morpholino)-ethanesulfonic acid.
- Received June 24, 2004.
- Accepted July 27, 2004.
- The American Society for Pharmacology and Experimental Therapeutics
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