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Inactive normal X in a female leukaemic patient with an acquired X/autosome translocation

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Summary

An X;9;22 translocation was detected in bone marrow cells of a female patient with blastic crisis of CML. A dynamic study following 5-BrdU treatment showed that the inactive late-replicating X chromosome was the normal one. This pattern of X-chromosome replication appears to be superimposable on the most usual model found in congenital X/autosome translocations.

It is suggested that preferential autosome translocation onto the active X chromosome could be the general rule in acquired X/autosome translocations associated with long survival.

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References

  • Alimena, G., Mandelli, F., Montuoro, A., Gastaldi, R., Dallapiccola, B.: Y chromosome duplication: a minor route evolutive pattern in CM. Acta Haematol. (Basel) (in press, 1979)

  • Cimino, M. C., Kinnealey, A., Variakojis, D., Golomb, H. M., Rowley, J. D.: Chromosomal abnormalities in patients with acute lymphocytic leukemia (ALL). Am. J. Hum. Genet. 29, 32 A (1977)

    Google Scholar 

  • Dutrillaux, B., Laurent, C., Gilgenkrantz, S., Frederic, J., Carpentier, S., Couturier, J., Lejeune, J.: Les translocations du chromosome X. Etude après traieement par le Budr et coloration par l'acridine orange. Helv. Paediatr. Acta 34, (Suppl.), 19–32 (1974)

    Google Scholar 

  • Engel, E., McGee, B., Flexner, J., Krantz, S. B.: Translocation of the Philadelphia chromosome onto the 17 short arm in chronic myeloid leukemia: a second example. N. Engl. J. Med. 293, 666 (1975)

    PubMed  Google Scholar 

  • Ford, J. H., Pittman, S. M., Singh, S., Was, E. J., Vincent, P. C., Gunz, F. W.: Cytogenetic basis of acute myeloid leukemia. Natl. Cancer Inst. 55, 761–765 (1975)

    Google Scholar 

  • Hayata, I., Sakurai, M., Kakati, S., Sandberg, A. A.: Chromosomes and causation of human cancer and leukemia. XVI. Banding studies of chronic myelocytic leukemia, including five unusual Ph' translocations. Cancer 36, 1177–1191 (1975)

    PubMed  Google Scholar 

  • Levan, G., Mitelman, F.: Loss of the late-replicating X chromosome in a female patient with acute myeloid leukemia and the 8;21 translocation: Brief communication. J. Natl. Cancer Inst. (in press, 1979)

  • Mattei, H. G., Mattei, J. F., Aymé, F., Malpuech, G., Giraud, F.: A dynamic study in two new cases of chromosome translocation. Hum. Genet. 41, 251–257 (1978)

    Article  PubMed  Google Scholar 

  • Mitelman, F., Nilsson, P. G., Levan, G., Brandt, L.: Non-random chromosome changes in acute myeloid leukemia. Chromosome banding examination of 30 cases at diagnosis. Int. J. Cancer 18, 31–38 (1976)

    PubMed  Google Scholar 

  • Morse, H. G., Ducore, J. M., Tays, T., Peakman, D., Robinson, A.: Multiple leukemic clones in acute leukemia of childhood. Hum. Genet. 40, 269–278 (1978)

    Article  PubMed  Google Scholar 

  • Oshimura, M., Freeman, A. I., Sandberg, A. A.: Chromosome and causation of human cancer and leukemia. XXVI. Banding studies in acute lymphoblastic leukemia (ALL). Cancer 40, 1161–1172 (1977)

    PubMed  Google Scholar 

  • Philip, P.: G-banding analysis of complex aneuploidy in a case of erythroleukaemia. Scand. J. Haematol. 16, 365–368 (1976)

    PubMed  Google Scholar 

  • Prigogina, E. L., Fleischman, E. W., Volkova, M. A., Frenkel, M. A.: Chromosome abnormalities and clinical and morphological manifestations of chronic myeloid leukemias. Hum. Genet. 41, 143–156 (1978)

    Article  PubMed  Google Scholar 

  • Rowley, J. D.: Identification of a translocation with quinacrine fluorescence in a patient with acute leukemia. Ann. Génét. (Paris) 16, 109–112 (1973)

    Google Scholar 

  • Rowley, J. D., Potter, D.: Chromosomal banding patterns in acute nonlymphocytic leukemia. Blood 47, 705–722 (1976)

    PubMed  Google Scholar 

  • Sakurai, M., Sandberg, A. A.: The chromosome and causation of human cancer and leukemia. XVIII. The missing Y in acute myeloblastic leukemia (AML) and Ph'-positive chronic myelocytic leukemia (CML). Cancer 38, 762–769 (1976)

    PubMed  Google Scholar 

  • Sakurai, M., Oshimura, M., Kakati, S., Sandberg, A. A.: 8–21 translocation and missing sex chromosome in acute leukaemia. Lancet 1974 II, 227–228

    Google Scholar 

  • Sonta, S. I., Sandberg, A. A.: Chromosome and causation of human cancer and leukemia. XXIX. Further studies on karyotypic progression in CML. Cancer 41, 153–163 (1978)

    PubMed  Google Scholar 

  • Therman, E., Patau, K.: Abnormal X chromosomes in man: Origin, behavior and effects. Humangenetik 25, 1–16 (1974)

    PubMed  Google Scholar 

  • Yamada, K., Furusawa, S.: Preferential involvement of chromosomes No. 8 and No. 21 in acute leukemia and preleukemia. Blood 47, 679–686 (1976)

    PubMed  Google Scholar 

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Dallapiccola, B., Alimena, G. Inactive normal X in a female leukaemic patient with an acquired X/autosome translocation. Hum Genet 48, 169–177 (1979). https://doi.org/10.1007/BF00286900

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  • DOI: https://doi.org/10.1007/BF00286900

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