Detection of chromosome 2 and chromosome 7 within X-ray- or colchicine-induced micronuclei by fluorescence in situ hybridization

Mutagenesis

Volumn 12, Issue 2, 1997, Pages 55-59

  Wuttke, K ^a   Streffer, C ^a   Muller W U ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COLCHICINE;

ARTICLE; CHROMOSOME 2; CHROMOSOME 7; CHROMOSOME PAINTING; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LYMPHOCYTE; MICRONUCLEUS; MICRONUCLEUS TEST; MULTINUCLEAR CELL; MUTAGENESIS; NORMAL HUMAN; PRIORITY JOURNAL; X RAY;

ANEUPLOIDY; CELL NUCLEUS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 7; COLCHICINE; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHOCYTES; MICRONUCLEUS TESTS; MITOTIC SPINDLE APPARATUS; X-RAYS;

EID: 0031002555     PISSN: 02678357     EISSN: None     Source Type: Journal    
DOI: 10.1093/mutage/12.2.55     Document Type: Article

References (26)

1. Adler, I.-D. (1993) Synopsis of the in vivo results obtained with the 10 known or suspected aneugens tested in the CEC collaborative study. Mutat. Res., 287, 131-137.
2. Alberts, B., Bray, D., Lewis, J., Raff, M., Roberts, K. and Watson, J.D. (eds) (1983) The Cytoskeleton. In Molecular Biology of the Cell. Garland Publishing, New York.
3. Bigner, S.H., Mark, J., Bullard, D.E., Mahaley, M.S., Jr and Bigner, D.D. (1986) Chromosomal evolution in malignant human gliomas starts with specific and usually numerical deviations. Cancer Genet. Cytogenet., 22, 121-135.
4. Bigner, S.H., Wong, A.J., Mark, J., Muhlbaier, L.H., Kinzler, K.W., Vogelstein, B. and Bigner, D.D. (1987) Relationship between gene amplification and chromosomal deviations in malignant gliomas. Cancer Genet. Cytogenet., 29, 165-170.
5. Brogger, A. (1977) Non-random localization of chromosome damage in human cells and targets for clastogenic action. In de la Chapelle, A. and Sorsa, M. (eds), Chromosomes Today. Elsevier, New York, pp. 297-306.
6. Cremer, T., Lichter, P., Borden, J., Ward, D.C. and Manuelidis, L. (1988) Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum. Genet., 80, 235-246.
7. Evans, H.J. (1988) Mutation cytogenetics: past, present and future. Mutat. Res., 204, 355-363.
8. Hando, J.C., Nath, J. and Tucker, J.D. (1994) Sex chromosomes, micronuclei and aging in women. Chromosoma, 103, 186-192.
9. Hayashi, M., Mäki-Paakkanen, J., Tanabe, H., Honma, M., Suzuki, T., Matsuoka, A., Mizusawa, H. and Sofuni, T. (1994) Isolation of micronuclei from mouse blood and fluorescence in situ hybridization with a mouse centromeric DNA probe. Mutat. Res., 307, 245-251.
10. Hayata, I. and Dutrillaux, B. (1985) Non-random involvement of rat and mouse chromosomes in the stable type chromosomal rearrangements observed in irradiated bone marrow cells. Proc. Jap. Acad., 61, 179-182.
11. Llombart-Bosch, A., Carda, C., Peydro-Olaya, A., Noguera, R., Boix, J., and Pellin, A. (1989) Pigmented esthesioneuroblastoma showing dual differentiation following transplantation in nude mice. Virchows Archiv A. Pathol. Anat., 414, 199-208.
12. Mendelsohn, M.L., Mayall, B.H., Bogart, E., Moore II, D.H. and Perry, B.H. (1973) DNA content and DNA-based centromeric index of the 24 human chromosomes. Science, 179, 1126-1129.
13. Müller, W.-U. and Streffer, C. (1994) Micronucleus Assays. Adv. Mutagen. Res., 5, 1-134.
14. Natarajan, A.T., Darroudi, F., Vermeulen, S. and Wiegant, J. (1992) Frequencies of X-ray and fast neutron induced chromosome translocations in human peripheral blood lymphocytes as detected by in situ hybridization using chromosome specific DNA libraries. In Sugahara, T., Sagan, L.A. and Aoyama, T. (eds), Low Dose Irradiation and Biological Defense Mechanisms. Elsevier Science Publishers, pp. 343-346.
15. Nickerson, J.A., He, D., Fey, G. and Penman, S. (1987) In Strauss, P.R. and Wilson, S.H. (eds), The Eukaryotic Nucleus. Molecular Biochemistry and Macromolecular Assemblies. Vol. 2. Telford Press, Caldwell, pp. 763-782.
16. Nüsse, M., Kramer, J. and Miller, B.M. (1992a) Factors influencing the DNA content of radiation-induced micronuclei. Int. J. Radiat. Biol., 62, 587-602.
17. Nüsse, M., Recknagel, S. and Beisker, W. (1992b) Micronuclei induced by 2-chlorobenzylidene malonitrile contain single chromosomes as demonstrated by the combined use of flow cytometry and immunofluorescent staining with anti-kinetochore antibodies. Mutagenesis. 7, 57-67.
18. Rey, J.A., Bello, J.M., de Campos, J.M., Kusak, M.E. and Moreno, S. (1987) On trisomy of chromosome 7 in human gliomas. Cancer Genet. Cytogenet., 29, 323-326.
19. Richard, F., Muleris, M. and Dutrillaux, B. (1994) The frequency of micronuclei with X chromosome increases with age in human females. Mutat. Res., 316, 1-7.
20. Sachs, L. (1984) Angewandte Statistik, 6th edn. Springer, Berlin.
21. Steel, C.M., Shade, M. and Woodward, M.A. (1980) Chromosome aberrations acquired in vitro by human B-cell lines I. Gains and losses of material. J. Natl. Cancer Inst., 64, 95-98.
22. Sternes, K.I. and Vig, B.K. (1989) Micronuclei, kinetochores and hypoploidy. Mutagenesis, 4, 425-431.
23. Steadman, J.S., Lee, L.W., Smith, G.J. and Grisham, J.W. (1994) DNA contents and chromosomes of clonal lines of transformed rat liver epithelial cells and of cells from their derived tumors. Carcinogenesis. 15, 963-969.
24. Takahashi, S., Qian, J., Brown, J.A., Alcaraz, A., Bostwick, D.G., Lieber, M.M and Jenkins, R.B. (1994) Potential markers of prostate cancer aggressiveness detected by fluorescence in situ hybridization in needle biopsies. Cancer Res., 54, 3574-3579.
25. Tawn, J. (1988) The non-random occurrence of exchanges involving chromosomes 7 and 14 in human lymphocytes: a prospective study of control individuals. Mutat. Res., 199, 215-220.
26. Weißenborn, U. and Streffer, C. (1991) Micronuclei with kinetochores in human melanoma cells and rectal carcinomas. Int. J. Radiat. Biol., 59, 373-383.