Functional genetic diversity in the high-affinity carnitine transporter OCTN2 (SLC22A5)
| Autor: | Kathleen M. Giacomini, Leah L. Lagpacan, Richard A. Castro, Claire M. Brett, Seymour Packman, Thomas J. Urban, Elaine J. Carlson, Renata C. Gallagher, Esteban G. Burchard, Chaline Brown, Travis R. Taylor, Thomas E. Ferrin |
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| Rok vydání: | 2006 |
| Předmět: |
Organic Cation Transport Proteins
Recombinant Fusion Proteins Molecular Sequence Data SLC22A5 Protein Structure Secondary Exon Open Reading Frames Carnitine medicine Coding region Humans Amino Acid Sequence RNA Messenger Allele Promoter Regions Genetic Solute Carrier Family 22 Member 5 Gene Peptide sequence Pharmacology Genetics Polymorphism Genetic biology Tetraethylammonium Molecular biology Fusion protein Protein Transport Genetics Population Phenotype Gene Expression Regulation biology.protein Molecular Medicine medicine.drug |
| Zdroj: | Molecular pharmacology. 70(5) |
| ISSN: | 0026-895X |
| Popis: | Systemic carnitine deficiency (SCD) is a rare autosomal recessive disease resulting from defects in the OCTN2 ( SLC22A5 ) gene, which encodes the high-affinity plasma membrane carnitine transporter. Although OCTN2 is fairly well studied in its relationship with SCD, little is known about the carrier frequency of disease-causing alleles of OCTN2, or of more common functional polymorphisms in this gene. To address these issues, we screened for genetic variants in the OCTN2 coding region by direct sequencing of the exons and flanking intronic region of OCTN2 in a large sample ( n = 276) of ethnically diverse subjects. In addition, we established lymphoblastoid cell lines from subjects homozygous for either allele of the previously identified promoter region variant, -207G>C. We found eight amino acid sequence variants of OCTN2, of which three (Phe17Leu, Leu144Phe, and Pro549Ser) were polymorphic in at least one ethnic group. When assayed for functional activity by expression in human embryonic kidney 293 cells, using as probes both the endogenous substrate (l-carnitine) and the organic cation tetraethylammonium, three variants showed functional differences from the reference OCTN2 (Phe17Leu, Tyr449Asp, Val481Phe; p < 0.05). Further studies of the Phe17Leu polymorphism showed a reduced V max for l-carnitine transport to approximately 50% of the reference OCTN2. Confocal microscopy studies using an OCTN2-GFP fusion protein showed that Phe17Leu had distinct subcellular localization from the reference OCTN2, with diffuse cytoplasmic retention of Phe17Leu, in contrast to reference OCTN2, which localized specifically to the plasma membrane. Lymphoblasts from subjects homozygous for the -207G allele showed increased l-carnitine transport compared with the -207C/C homozygotes ( p < 0.05). This study suggests that although loss-of-function mutations in OCTN2 are likely to be rare, common variants of OCTN2 found in healthy populations may contribute to variation in the disposition of carnitine and some clinically used drugs. |
| Databáze: | OpenAIRE |
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