This report describes the isolation, nucleotide sequencing, and functional expression of human cDNAs that restore reduced folate carrier activity in transport-defective cells. Based on homology to a partial murine cDNA probe, two functional cDNAs were isolated from a lambda gt11 library prepared from methotrexate transport upregulated K562 cells (K562.4CF). A 2.8-kilobase (kb) clone, KS43, contained a 1776-base pair open reading frame. The 2.5-kb clone, KS32, contained an internal deletion (626 base pairs) resulting a shortened open reading frame and 3'-untranslated region. KS43 and KS32 encoded proteins with multiple hydrophobic domains, one consensus N-glycosylation site, and predicted molecular masses of 65 and 58 kDa, respectively. The deduced amino acid sequence of KS43 is 79% and 80% homologous to the mouse and hamster sequences, respectively (Dixon, K. H., Lanpher, B. C., Chiu, J., Kelley, K., and Cowan, K. H. (1994) J. Biol. Chem. 269, 17-20; Williams, F. M. R., Murray R. C., Underhill, T. M., and Flintoff, W. F. (1994) J. Biol. Chem. 269, 5810-5816). Northern blots identified one primary transcript at 3.1 kb in parental K562, K562.4CF, and transport-impaired K500E cells; transcript levels varied by 7-fold. The expression of both KS43 and KS32 in methotrexate transport-defective Chinese hamster ovary cells restored methotrexate sensitivity and transport. Certain transport characteristics of the transfected cells resembled both the wild type human (K562) and hamster "classical" reduced folate carriers, suggesting the expression of a hybrid system. For instance, based on Ki values, up to a 4-fold increased affinity for 1843U89 over wild type hamster cells (typical of human cells), and a 19-fold increased affinity for methotrexate over K562 cells (typical of hamster cells) was observed. Further, a photoaffinity probe with high specificity for the reduced folate carrier labeled 94-kDa proteins in K562 cells and the transfectant containing the full-length KS43, and a 85-kDa protein in the transfectant containing the 3'-truncated KS32. No specifically labeled proteins were detected in wild type or mock-transfected hamster cells. Collectively, our results suggest that the KS43/KS32 cDNAs encode the human reduced folate carrier; however, additional modulatory/regulatory factors may be required to manifest the full spectrum of transport substrate activities typical of this system.

The basis for impaired reduced folate carrier (RFC) activity in methotrexate-resistant CCRF-CEM (CEM/ Mtx-1) cells was examined. Parental and CEM/Mtx-1 cells expressed identical levels of the 3.1-kilobase RFC transcript. A ϳ85-kDa RFC protein was detected in parental cells by photoaffinity labeling and on Western blots with RFC-specific antiserum. In CEM/Mtx-1 cells, RFC protein was undetectable. By reverse transcriptase-polymerase chain reaction and sequence analysis, G to A point mutations were identified in CEM/ Mtx-1 transcripts at positions 130 (P 1 ; changes glycine 44 3 arginine) and 380 (P 2 ; changes serine 127 3 asparagine Despite the availability of newer antifolates, methotrexate (Mtx) 1 continues to play an important role as an antineoplastic agent. To reach its intracellular target, dihydrofolate reductase, the preferred route of Mtx entry involves the reduced folate carrier (RFC; 1, 2). RFC transport of Mtx is critical to drug action because of its role in generating sufficient unbound intracellular antifolate to sustain maximal enzyme inhibition (1). Furthermore, high levels of Mtx are also necessary for the synthesis of Mtx polyglutamates (1).Defective membrane transport of Mtx by RFC has been identified as a major mechanism of Mtx resistance (1-11). Transport alterations can manifest as reduced rates of carrier translocation (reduced V max ), decreased affinities for transport substrates (increased K t ), or both, and may involve decreased levels of normal RFC (6) or the expression of structurally altered RFC proteins (7-11). For instance, in Mtx-resistant K562 (K500E) cells, impaired Mtx transport is accompanied by decreased RFC transcripts and protein (6). A G to A transition at position 890 of the murine RFC cDNA resulted in a substitution of serine 297 by asparagine and a selective decrease in Mtx binding affinity (ϳ4-fold) without effects on other antifolate analogs (aminopterin, Ref. 9). Likewise, replacement of serine 46 by asparagine (10) or glutamate 45 by lysine (11) in murine RFC resulted in greater impairment of uptake for Mtx than (6S)-5-formyl tetrahydrofolate. In severely transport defective L1210 cells (Mtx r A), loss of transport activity appeared to reflect a single (G to C) point mutation at nucleotide 429 of the murine RFC cDNA sequence which resulted in the substitution of proline 130 by alanine (7). However, these cells also contained a wild-type RFC allele that was not transcribed. A silent wild-type RFC allele was described for Mtx-resistant MOLT-3 cells (MOLT-3/Mtx 10,000 ; Ref. 8). Moreover, two mutations in the RFC coding region were detected which resulted in the creation of new stop codons and synthesis of truncated nonfunctional RFCs (8).In this report, the molecular mechanisms responsible for the transport-impaired phenotype (ϳ3% of wild-type) of Mtx-resistant (ϳ243-fold) CCRF-CEM (CEM/Mtx-1;12) cells were examined. We show that although the levels of RFC transcripts are essentially unchanged from wild-type cells, there is a complete loss of RFC protein due to ear...

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The role of N-glycosylation in reduced folate carrier (RFC) transport and membrane targeting was examined in transport-deficient K562 (K500E) cells transfected with human RFC cDNAs. Treatment of cells expressing wild-type RFC with tunicamycin (0-3 microg) resulted in a progressive shift of the approximately 85 kDa RFC on western blots to 65 kDa. At 3 microg/ml tunicamycin, the nearly complete loss of glycosylated RFC was accompanied by a approximately 25% decreased rate of methotrexate uptake. A deglycosylated RFC cDNA construct in which asparagine-58 was replaced by glutamine (Gln58-RFC) was expressed in K500E cells as a 65 kDa protein and restored transport capacity for methotrexate and (6S)5-formyl tetrahydrofolate. With both wild-type and Gln58-RFC constructs, expression of cDNA-encoded RFC protein far exceeded relative levels of RFC uptake. Wild-type and Gln58-RFCs containing a hemagglutinin (HA) epitope at the carboxyl terminus were similarly functional and, by immunofluorescence staining with rhodamine-conjugated anti-HA antibody, were localized to plasma membranes. Collectively, our results demonstrate that N-glycosylation of human RFC plays no significant role in either transport function or membrane targeting. The discrepancy between the stoichiometries of RFC expression and transport activity for both wild-type RFC and Gln58-RFC implies that identical regulatory controls and/or non-RFC transport components are necessary to completely restore transport function in the transfected cells.