Abstract
The gene for human prothrombin, or factor II (F2) has been assigned to 11p11–q12 by the combined use of a panel of somatic cell hybrid DNAs and in situ hybridization, using both cDNA and genomic probes. In addition, the cDNA probe for F2 recognizes a homologous sequence which has been tentatively mapped to the X chromosome. Similar approaches have been used to confirm the assignment of the ceruloplasmin gene, but to regionally localize it more proximally than previously reported (3q21–q24). These results provide further evidence that genes encoding the coagulation factors and related proteins are dispersed throughout the human genome.
Literature cited
Jackson, C.M., and Nemerson, Y. (1980).Annu. Rev. Biochem. 49:765–811.
McKusick, V.A. (1983).Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive and X-Linked Phenotypes, 6th ed. (Johns Hopkins University Press, Baltimore).
Vehar, G.A., Keyt, B., Eaton, D., Rodriquez, H., O'Brien, D.P., Rotblat, F., Oppermann, H., Keck, R., Wood, W.I., Harkins, R.N., Tuddenham, E.G.D., Lawn, R.M., and Capon, D.J. (1984).Nature 312:337–342.
Toole, J.J., Knopf, J.L., Wozney, J.M., Sultzman, L.A., Buecker, J.L., Pittman, D.D., Kaufman, R.J., Brown, E., Shoemaker, C., Orr, E.C., Amphlett, G.W., Foster, W.B., Coe, M.L., Knutson, G.J., Fass, D.N., and Hewick, R.M. (1984).Nature 312:342–347.
Church, W.R., Jernigan, R.L., Toole, J., Hewick, R.M., Knopf, J., Knutson, G.J., Nesheim, M.E., Mann, K.G. and Fass, D.N. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:6934–6937.
Takahashi, N., Ortel, T., and Putman, F.W. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:390–394.
Yang, F., Naylor, S.L., Luin, J.B., Cutshaw, S., McCombs, J.L., Naberhans, K.H., McGill, J.R., Adrian, G.S., Moore, C.M., Barnett, D.R. (1986).Proc. Natl. Acad. Sci. U.S.A. 83:3257–3261.
Koschinsky, M.L., Funk, W.D., van Oost, B.A., MacGillivray, R.T.A. (1986).Proc. Natl. Acad. Sci. U.S.A. 83:5086–5090.
Yang, F., Lum, J.B., McGill, J.R., Moore, C.M., Naylor, S.L., van Bragt, P.H., Baldin, W.D., Bowman, B.H. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:2752–2756.
Rabin, M., McClelland, A., Kuhn, L., and Ruddle, F.H. (1985).Am. J. Hum. Genet. 37:1112–1116.
McKusick, V.A., and Conneally, P.M. (1984).Cytogenet. Cell Genet. 37:205–209.
MacGillivray, R.T.A., Irwin, D.M., Guinto, E.R., and Stone, J.C. (1986).Ann. N.Y. Acad. Sci. (in press).
Lawn, R.M., Fritsch, E.F., Parker, R.C., Blake, G., and Maniatis, T. (1978).Cell 15:1157–1174.
Degen, S.J.F., MacGillivray, R.T.A., and Davie, E.W. (1983).Biochemistry 22:2087–2097.
Vieira, J., and Messing, J. (1982).Gene 19:259–268.
Donald, L.J., Wang, H.S., Kamali, V., Liebert, L., Rudner-Marion, M., Cameron, E.S., Riddell, D.C., Vust, A., Wrogemann, K., and Hamerton, J.L. (1983).Cytogenet. Cell Genet. 37:453A.
Southern, E.M. (1975).J. Mol. Biol. 98:503–517.
Lin, C.C., Draper, P.N., and DeBrackeleer, M. (1985).Cytogenet. Cell. Genet. 39:269–274.
Harper, M.A., and Saunders, G.F. (1981).Chromosoma 83:431–439.
Royle, N.J., Fung, M.R., MacGillivray, R.T.A., and Hamerton, J.L. (1986).Cytogenet. Cell Genet. 41:185–188.
Chance, P.F., Dyer, K.A., Kurachi, K., Yoshitake, S., Ropers, H.H., Wieacker, P., and Gartier, S.M. (1983).Hum. Genet. 65:207–208.
Boyd, Y., Buckle, V.J., Munroe, E.A., Choo, K.H., Migeon, B.R., and Craig, I.W. (1984).Ann. Hum. Genet. 48:145–152.
Camerino, G., Grzeschik, K.H., Jaye, M., De La Jalle, H., Tolstoshev, P., Lecocq, J.P., Heilig, R., and Mandel, J.L. (1984).Proc. Natl. Acad. Sci. U.S.A. 81:498–502.
Degen, S.J.F., MacGillivray, R.T.A., and Davie, E.W. (1983). InManipulation and Expression of Genes in Eukaryotes, (eds.) Nagley, P., Linnane, A.W., Peacock, W.J., and Pateman, J.A. (Academic Press, Sydney), pp. 13–16.
Human Gene Mapping 8 (1985). Conference.Cytogenet. Cell Genet. 40:1–823.
Kant, J.A., Forance, A.J., Saxe, D., Simon, M.I., McBride, O.W., and Crabtree, G.R. (1985).Proc. Natl. Acad. Sci. U.S.A. 82:2344–2348.
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Royle, N.J., Irwin, D.M., Koschinsky, M.L. et al. Human genes encoding prothrombin and ceruloplasmin map to 11p11–q12 and 3q21–24, respectively. Somat Cell Mol Genet 13, 285–292 (1987). https://doi.org/10.1007/BF01535211
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DOI: https://doi.org/10.1007/BF01535211