Abstract
p97 is a 97,000 molecular weight cell-surface glycoprotein, which is present in human melanomas but in only trace amounts in normal adult tissues1–4. Amino acid sequence and iron binding studies have shown that p97 is structurally and functionally related to transferrin5. Reports that the genes for the transferrin receptor (TR)6–8 and possibly transferrin9–13 are located on chromosome 3 prompted us to investigate the chromosomal localization of the p97 gene. Our strategy was to characterize interspecies somatic cell hybrids derived from human fibroblasts or lymphocytes for expression of p97 and presence of human chromosomes. Although fibroblasts and lymphocytes express only small amounts of p973,4, we were able to type the hybrids for p97 by using monoclonal antibodies in highly sensitive and specific immunoassays. Of 14 hybrids, 6 contained chromosome 3 and expressed p97, and 8 were negative for both. We conclude that the p97 gene, like the transferrin and TR genes, is located on chromosome 3.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Complex of human Melanotransferrin and SC57.32 Fab fragment reveals novel interdomain arrangement with ferric N-lobe and open C-lobe
Scientific Reports Open Access 12 January 2021
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Rent or buy this article
Get just this article for as long as you need it
$39.95
Prices may be subject to local taxes which are calculated during checkout
References
Woodbury, R. G., Brown, J. P., Yeh, M-Y., Hellström, I. & Hellström, K. E. Proc. natn. Acad. Sci. U.S.A. 77, 2183–2186 (1980).
Brown, J. P., Nishiyama, K., Hellström, I. & Hellström, K. E. J. Immun. 127, 539–546 (1981).
Brown, J. P., Woodbury, R. G., Hart, C. E., Hellström, I. & Hellström, K. E. Proc. natn. Acad. Sci. U.S.A. 78, 539–543 (1981).
Woodbury, R. G., Brown, J. P., Loop, S. M., Hellström, K. E. & Hellström, I. Int. J. Cancer 27, 145–149 (1981).
Brown, J. P. et al. Nature 296, 171–173 (1982).
Goodfellow, P. M. et al. Somatic Cell Genet. 8, 197–206 (1982).
Enns, C. A., Suomaliainen, H. A., Gebhardt, J. E., Schröder, J. & Sussman, H. H. Proc. natn. Acad. Sci. U.S.A. 79, 3241–3245 (1981).
Miller, Y., Seligman, P., Jones, C., Patterson, D. & Scoggin, C. Clin. Res. 30, 41A (1982).
McAlpine, P. J. & Bootsma, D. Cytogenet. Cell Genet. 32, 121–129 (1982).
Maylor, S. L., Lalley, P. A., Elliot, R. W., Brown, J. A. & Shows, T. B. Am. J. hum. Genet. 32, 159A (1980).
Naylor, S. L., Shows, T. B. & Klebe, R. J. Somat. Cell Gent. 5, 11–21 (1979).
Voss, R., Lerer, I., Povey, S., Solomon, F. & Bobrow, M. Ann. hum. Genet. 44, 1–9 (1980).
Shows, T. B., Scrafford Wolff, C. R., Brown, J. A. & Meisler, M. H. Somat. Cell Genet. 5, 147–158 (1979).
Kucherlapati, R., Tepper, R., Granelli-Piperno, A. & Reich, E. Cell 15, 1331–1340 (1978).
Omary, M. B., Trowbridge, I. S. & Minowada, J. M. Nature 268, 888–891 (1980).
Trowbridge, I. S. & Omary, M. B. Proc. natn. Acad. Sci. U.S.A. 78, 3039–3043 (1981).
Suomalainen, H. A., Goldsby, R. A., Osborne, B. A. & Schröder, J. Scand. J. Immun. 11, 163–168 (1980).
Wyandt, H. E., Wysham, D. G., Minden, S. K., Anderson, R. S. & Hecht, F. Expl Cell Res. 102, 85–94 (1976).
Seabright, M. Lancet ii, 971–972 (1971).
Enns, C. A., Shindelman, J. E., Tonik, S. E. & Sussman, H. H. Proc. natn. Acad. Sci. U.S.A. 78, 4222–4225 (1981).
Cleveland, D. W., Fischer, S. G., Kirschner, M. W. & Laemmli, U. K. J. biol. Chem. 252, 1102–1106 (1977).
Goubin, G., Goldman, D. S., Luce, J., Neimain, P. E. & Cooper, G. M. Nature 302, 114–119 (1983).
Mitelman, F. & Levan, G. Hereditas 95, 79–139 (1981).
Haynes, B. F. et al. J. Immun. 127, 347–351 (1981).
Judd, W., Poodry, C. A. & Strominger, J. L. J. exp. Med. 152, 1430–1435 (1980).
Larrick, J. W. & Logue, G. Lancet ii, 862–863 (1980).
Shindelman, J. E., Ortmeyer, A. E. & Sussman, H. H. Int. J. Cancer 27, 329–334 (1981).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Plowman, G., Brown, J., Enns, C. et al. Assignment of the gene for human melanoma-associated antigen p97 to chromosome 3. Nature 303, 70–72 (1983). https://doi.org/10.1038/303070a0
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/303070a0
This article is cited by
-
Complex of human Melanotransferrin and SC57.32 Fab fragment reveals novel interdomain arrangement with ferric N-lobe and open C-lobe
Scientific Reports (2021)
-
The melanoma tumor antigen, melanotransferrin (p97): a 25-year hallmark – from iron metabolism to tumorigenesis
Oncogene (2007)
-
Identification of a Novel Route of Iron Transcytosis across the Mammalian Blood-Brain Barrier
Microcirculation (2003)
-
Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybrids
Somatic Cell and Molecular Genetics (1988)
-
Heterogeneity of the human transferrin receptor and use of anti-transferrin receptor antibodies to detect tumoursin vivo
Immunology and Cell Biology (1987)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.