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Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures

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Summary

A correlation between specific fragile sites and cancer breakpoints has been suggested raising the question of fragile site expression as a predisposing factor in the occurrence of cancer in some persons. Before addressing the question of increased fragility among patients at high risk for cancer, we analyzed the variability of aphidicolin-induced fragile sites among nine normal persons and also among repeated samples from three of these individuals. Considerable variation in both the frequency and location of these fragile sites was observed and the data strongly suggest the significant variation of 6 of the 16 selected sites to be primarily due to sampling differences. These findings indicate that the use of fragile sites as a screening tool for patients at high risk of cancer should be carefully monitored relative to the variation inherent in both culture and individual expression.

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References

  • Brookwell R, Daniel A, Turner G, Fishburn J (1982) The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes. Am J Med Genet 13:139–148

    Google Scholar 

  • Daniel A (1986) Clinical implications and classification of the constitutive fragile sites. Am J Med Genet 23:419–427

    Google Scholar 

  • Daniel A, Ekblom L, Phillips S (1984) Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X). Am J Med Genet 18:483–491

    Google Scholar 

  • De Braekeleer M, Smith B, Lin CC (1985) Fragile sites and structural rearrangements in cancer. Hum Genet 69:112–116

    Google Scholar 

  • Glover TW, Berger C, Coyle J, Echo B (1984) DNA polymerase a-inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136–142

    Google Scholar 

  • Glover TW, Coyle-Morris J, Morgan R (1986) Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression. Cancer Genet Cytogenet 19:141–150

    Google Scholar 

  • Gollin SM, Perrot LJ, Gray BA, Kletzel M (1986) Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11). Cancer Genet Cytogenet 20:331–339

    Google Scholar 

  • Hecht F, Glover TW (1984) Cancer chromosome breakpoints and common fragile sites induced by aphidicolin. Cancer Genet Cytogenet 13:185–188

    Google Scholar 

  • Hecht F, Hecht BK (1986) Chromosome 9 in acute lymphoblastic leukemia: breaks in band 9p21-22 and a fragile site. Cancer Genet Cytogenet 21:1–3

    Google Scholar 

  • Jacobs PA, Glover TW, Mayer M, Fox P, Gerrard JW, Dunn HG, Herbst DS (1980) X-linked mental retardation: a study of 7 families. Am J Med Genet 7:471–489

    Google Scholar 

  • Le Beau MM (1986) Chromosomal fragile sites and cancer-specific rearrangements. Blood 67:849–858

    Google Scholar 

  • Le Beau MM, Rowley JD (1984) Heritable fragile sites and cancer. Nature 308:607–608

    Google Scholar 

  • Michels VV (1985) Fragile sites on human chromosomes: description and clinical significance. Mayo Clin Proc 60:690–696

    Google Scholar 

  • Shabtai F, Klar D, Hart J, Halbrecht I (1985) On the meaning of fragile sites in cancer risk and development. Cancer Genet Cytogenet 18:81–85

    Google Scholar 

  • Sutherland GR (1985) Heritable fragile sites on human chromosomes. XII. Population cytogenetics. Ann Hum Genet 49:153–161

    Google Scholar 

  • Sutherland GR, Hecht F (1985) Fragile sites on human chromosomes. Oxford University Press, New York Oxford

    Google Scholar 

  • Sutherland GR, Parslow MI, Baker E (1985) New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine. Hum Genet 69:233–237

    Google Scholar 

  • Yunis JJ (1984) Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia. Cancer Genet Cytogenet 11:125–137

    Google Scholar 

  • Yunis JJ, Soreng AL (1984) Constitutive fragile sites and cancer. Science 226:1199–1204

    Google Scholar 

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Craig-Holmes, A.P., Strong, L.C., Goodacre, A. et al. Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures. Hum Genet 76, 134–137 (1987). https://doi.org/10.1007/BF00284909

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  • DOI: https://doi.org/10.1007/BF00284909

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