Cited by 827Iron Metabolism and DisordersNeurological diseases and metabolismHemoglobinopathies and Related Disorders

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The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

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Feder, John N., Penny, David M., Irrinki, Alivelu, Lee, Vince K., Lebrón, José A., Watson, Nicole, Tsuchihashi, Zenta, Sigal, Elliott, Bjorkman, Pamela J., Schatzman, Randall C.·1998·Proceedings of the National Academy of Sciences

DOI 10.1073/pnas.95.4.1472PMC PMC19050

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Abstract

We recently reported the positional cloning of a candidate gene for hereditary hemochromatosis called HFE . The gene product, a member of the major histocompatibility complex class I-like family, was found to have a mutation, Cys-282 → Tyr (C282Y), in 85% of patient chromosomes. This mutation eliminates the ability of HFE to associate with β 2 -microglobulin (β 2 m) and prevents cell-surface expression. A second mutation that has no effect on β 2 m association, H63D, was found in eight out of nine patients heterozygous for the C282Y mutant. In this report, we demonstrate in cultured 293 cells overexpressing wild-type or mutant HFE proteins that both the wild-type and H63D HFE proteins form stable complexes with the transferrin receptor (TfR). The C282Y mutation nearly completely prevents the association of the mutant HFE protein with the TfR. Studies on cell-associated transferrin at 37°C suggest that the overexpressed wild-type HFE protein decreases the affinity of the TfR for transferrin. The overexpressed H63D protein does not have this effect, providing the first direct evidence for a functional consequence of the H63D mutation. Addition of soluble wild-type HFE/β 2 m heterodimers to cultured cells also decreased the apparent affinity of the TfR for its ligand under steady-state conditions, both in 293 cells and in HeLa cells. Furthermore, at 4°C, the added soluble complex of HFE/β 2 m inhibited binding of transferrin to HeLa cell TfR in a concentration-dependent manner. Scatchard plots of these data indicate that the added heterodimer substantially reduced the affinity of TfR for transferrin. These results establish a molecular link between HFE and a key protein involved in iron transport, the TfR, and raise the possibility that alterations in this regulatory mechanism may play a role in the pathogenesis of hereditary hemochromatosis.

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
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Authors: Feder, J. N., Penny, D. M., Irrinki, A., Lee, V. K., Lebrón, J. A., Watson, N., Tsuchihashi, Z., Sigal, E., Bjorkman, P. J., & Schatzman, R. C.
Affiliations: California Institute of Technology (US)
Progenitor, Inc. (formerly Mercator Genetics, Inc.), 4040 Campbell Avenue, Menlo Park, CA 94025; and Division of Biology 156-29 and Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125
ORCID: Feder, John N.
Irrinki, Alivelu
Lebrón, José A.
Tsuchihashi, Zenta
Venue: Proceedings of the National Academy of Sciences
Publisher: National Academy of Sciences
Published: 1998-02-17
Volume: 95
Issue: 4
Pages: 1472-1477
ISSN: 0027-8424 (ISSN-L)
1091-6490
DOI: 10.1073/pnas.95.4.1472
PMC: PMC19050
OpenAlex: W2141937988
Cited by: 827
References: 28
Citations by year: 2026: 3 · 2025: 4 · 2024: 4 · 2023: 9 · 2022: 7 · 2021: 7 · 2020: 14 · 2019: 7 · 2018: 10 · 2017: 16 · 2016: 24 · 2015: 21 · 2014: 18 · 2013: 28 · 2012: 26
FWCI: 51.51
Type: journal article
Language: en
Open access: green
europepmc.org
Locations: Proceedings of the National Academy of Sciences (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
CaltechAUTHORS (California Institute of Technology) (submittedVersion)
Topics: Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
Keywords: hereditary hemochromatosis, HFE gene, transferrin receptor, C282Y mutation, H63D mutation, beta2-microglobulin, protein complex formation, iron transport, pathogenesis
MeSH terms: Hemochromatosis Protein, Amino Acid Sequence, beta 2-Microglobulin, Hemochromatosis, HLA Antigens, Humans, Ligands, Membrane Proteins, Precipitin Tests, Protein Binding, Receptors, Transferrin, Structure-Activity Relationship, Transfection, Transferrin, Histocompatibility Antigens Class I, Point Mutation, Dimerization

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The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

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