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Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia

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Summary

Rearrangement of the breakpoint cluster region (bcr) and the chromosomal location of c-abl and 3′-bcr were studied in two patients with Philadelphia chromosome (Ph1)-negative chronic myelocytic leukemia (CML). One patient (patient 1) had a normal karyotype and the other (patient 2), 46,XY,inv(3)(q21q26). Both patients showed the bcr rearrangement by Southern blot analysis with a 1.2 kb 3′-bcr probe. In situ hybridization studies demonstrated the location of the homologous sequences of bcr on chromosome 22 in patient 1, and on chromosomes 9 and 22 in patient 2. These findings indicate that the morphologically normal-looking chromosomes 9 and 22 in patient 2 are the result of a retranslocation between chromosomes 9q+ and 22q-, abnormalities which were first formed by a standard Ph1 translocation.

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References

  • Ben-Neriah Y, Daley GQ, Nes-Messon AM, Witte ON, Baltimore D (1986) The chronic myelogenous leukemia-specific p210 protein in the product of the bcr-abl hybrid gene. Science 233:212–219

    Google Scholar 

  • Dreazen O, Klisak I, Rassool F, Goldman JM, Sparkes RS, Gale RP (1987) Do oncogenes determine clinical features in chronic myelocytic leukaemia? Lancet II:1402–1405

    Google Scholar 

  • Ganesan TS, Rassool F, Guo A-P, Th'ng KH, Dowding C, Hibbin JA, Young BD, White H, Kumaran TO, Galton DAG, Goldman JM (1986) Rearrangement of the bcr gene in Philadelphia chromosome-negative myeloid leukemia. Blood 68:957–960

    Google Scholar 

  • Harper ME, Saunders GF (1981) Localization of single copy of DNA sequences on G-banded human chromosomes by in situ hybridization. Chromosoma 83:431–439

    Google Scholar 

  • ISCN (1985) An international system for human cytogenic nomenclature. Harnden DG, Klinger HP (eds) Published in collaboration with Cytogenet Cell Genet. Karger, Basel

    Google Scholar 

  • Ishihara T, Minamihisamatsu M (1988) The Philadelphia chromosome consideration based on studies of variant translocation. Cancer Genet Cytogenet 32:75–92

    Google Scholar 

  • Konopka JB, Watanabe SM, Singer JW, Collins SJ, Witte ON (1985) Cell lines and clinical isolates derived from Ph-positive chronic myelogenous leukemia patients express c-abl proteins with a common structural alteration. Proc Natl Acad Sci USA 821:1810–1814

    Google Scholar 

  • Morris CM, Reeve AE, Fitzgerald PH, Hollings PE, Beard MEJ, Heaton DC (1986) Genomic diversity correlates with clinical variation in Ph1-negative chronic myeloid leukaemia. Nature 320:281–283

    Google Scholar 

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Inazawa, J., Nishigaki, H., Takahira, H. et al. Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia. Hum Genet 83, 115–118 (1989). https://doi.org/10.1007/BF00286701

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  • DOI: https://doi.org/10.1007/BF00286701

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