Abstract
The structural gene for purine-nucleoside phosphorylase (NP) has been assigned to a subregion of chromosome 14 by somatic cell hybridization of male and female cells containing the balanced translocation t(X;14) (p22;q21). Peripheral lymphocytes were fused to a pseudodiploid HPRT-deficient established Chinese hamster cell line. 23 primary hybrid clones (10 derived from male and 13 from female cells) were isolated and maintained in HAT selective medium. Parallel subcultures from generations 16, 24, and 40 after clonal isolation were fully karyotyped and analyzed electrophoretically for expression of the human types of NP, HPRT, G6PD, and PGK. The human NP phenotype segregated discordantly with each human chromosome except chromosome 14 and the der(14),t(X;14) translocation chromosome. In all, 8 hybrids which had retained the der(X), t(X;14) translocation chromosome under HAT selective pressure and expressed human HPRT had lost the human NP phenotype. These results indicate localization of the NP gene in region 14pter→14q21.
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Literature cited
Ruddle, F. H. (1972).Adv. Hum. Genet. 3:173–236.
1974 Rotterdam Conference. (1975).Second International Workshop on Human Gene Mapping, Birth Defects: Original Article Series, Vol. 11, No. 3, The National Foundation, New York.
Burgerhout, W., v. Someren, H., and Bootsma, D. (1973).Humangenetik 20:159–162.
Grzeschik, K. H., Allderdice, P. W., Grzeschik, K. A., Opitz, J. M., Miller, O. J., and Siniscalco, M. (1972).Proc. Natl. Acad. Sci. U. S. A. 69:69–73.
1973 New Haven Conference. (1974).First International Workshop on Human Gene Mapping, Birth Defects: Original Article Series, Vol. 10, No. 3, The National Foundation, New York.
Francke, U., and Busby, N. (1975). 1974 Rotterdam Conference.Second International Workshop on Human Gene Mapping, Birth Defects: Original Article Series. Vol. 2, No. 3. The National Foundation, New York, 143–149.
Francke, U. (1975). 1974 Rotterdam Conference.Second International Workshop on Human Gene Mapping, Birth Defects: Original Article Series, Vol 2, No. 3. The National Foundation, New York, 138–142.
1971 Paris Conference. (1972).Standardization in Human Cytogenetics, Birth Defects: Original Article Series, Vol 8, No. 7, The National Foundation, New York.
Ricciuti, R. and Ruddle, F. H. (1973).Nature (London) New Biol. 241:180–182.
Edwards, Y. H., Hopkinson, D. A., and Harris, H.(1971).Ann. Hum. Genet. 34:395–408.
Giblett, E. R., Ammann, A. J., Sandman, R., Wara, D. W., and Diamond, L. K. (1975).Lancet 1:1010–1013.
Peterson, R.M., Paulson, S.D., Wilson, M.G., and Towner, J. W. (1970).Clin. Res. 18:207. (Abstract)
Chu, E.H.Y., Brimer, P., Jacobson, K.B., and Merriam, E.V. (1969).Genetics 62:359–377.
Croce, C.M., Koprowski, H., and Eagle, H. (1972).Proc. Natl. Acad. Sci. U.S.A. 69:1953–1956.
Coon, H.G., and Weiss, M.C. (1969).Proc. Natl. Acad. Sci. U.S.A. 62:852–859.
Littlefield, J.W. (1964).Science 145:709–710.
Schmid, W. (1963).Cytogenetics 2:175–193.
Meera Khan, P. (1971).Arch. Biochem. Biophys. 145:470–483.
v. Someren, H., v. Henegouwen, H. B., Los, W., Wurzer-Figurelli, E., Doppert, B., Vervloet, M., and Meera Khan, P. (1974).Humangenetik 25:189–201.
Bakay, B., and Nyhan, W.L. (1971).Biochem. Genet. 5:81–90.
Bakay, B., Nyhan, W.L., Croce, C.M., and Koprowski, H. (1975).J. Cell Sci. 17:567–579.
Cohen, M.M., Lin, C.-C., Sybert, V., and Orecchio, E. J. (1972).Am. J. Hum. Genet. 24:583–597.
Ricciuti, F., and Ruddle, F.H. (1973).Genetics 74:661–678.
Hamerton, J.I., Douglas, G.R., Gee, P.A., and Richardson, B.J. (1973).Cytogenet. Cell Genet. 12:128–135.
Creagan, R.P., Tan, Y.H., Chen, S., Tischfield, J.A., and Ruddle, F.H. (1974). 1973 New Haven Conference.First International Workshop on Human Gene Mapping, Birth Defects: Original Article Series, Vol. 10, No. 3, The National Foundation, New York, 83–85.
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Francke, U., Busby, N., Shaw, D. et al. Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen→14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation. Somat Cell Mol Genet 2, 27–40 (1976). https://doi.org/10.1007/BF01539240
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DOI: https://doi.org/10.1007/BF01539240
Keywords
- Nucleoside
- Phosphorylase
- Interspecific Hybridization
- Cell Hybridization
- Translocation Chromosome