Chromosome painting of radiation-induced micronuclei

International Journal of Radiation Biology

Volumn 70, Issue 4, 1996, Pages 393-401

  Slavotinek, A ^a   Sauer Nehls, S ^b   Braselmann, H ^c   Taylor, G M ^d   Nusse M ^b  

^a OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

^c Institut für Strahlenbiologie   (Germany)

^d ST MARY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME PAINTING; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GAMMA RADIATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; MICRONUCLEUS; PRIORITY JOURNAL;

CELL DIVISION; CELL LINE; CELL NUCLEUS; CHROMOSOMES, HUMAN; CYTOCHALASIN B; CYTOGENETICS; FLUORESCEIN-5-ISOTHIOCYANATE; HUMANS; IN SITU HYBRIDIZATION; KARYOTYPING; LYMPHOCYTES; MICRONUCLEI, CHROMOSOME-DEFECTIVE;

EID: 0029822691     PISSN: 09553002     EISSN: None     Source Type: Journal    
DOI: 10.1080/095530096144860     Document Type: Article

References (32)

1. BARRIOS, L., MIRÓ, R., CABALLİN, M. R., FUSTER, C., GUEDEA, F., SUBIAS, A. and EGOZCUE, J. 1989, Cytogenetic effects of radiotherapy. Breakpoint distribution in induced chromosome aberrations. Cancer Genetics and Cytogenetics, 41, 61-70.
2. BAUCHINGER, M. and GÖTZ, G., 1979, Distribution of radiation induced lesions in human chromosomes and dose-effect relation analysed with G-banding. Radiation Environmental Biophysics, 16, 355-366.
3. BAUCHINGER, M., SCHMID, E., ZITZELSBERGER, H., BRASELMANN, H. and NAHRSTEDT, U., 1993, Radiation-induced chromosome aberrations analysed by two-colour fluorescence in situ hybridization with composite whole chromosome-specific DNA probes and a pancentromeric DNA probe. International Journal of Radiation Biology, 64, 179-184.
4. BEISKER, W., 1994, A new combined integral-light and slit scan data analysis system (DAS) for flow cytometry. Computer Methods and Programming in Biomedicine, 42, 15-26.
5. BOEI, J. J. W. A. and NATARAJAN, A. T., 1995, Detection of chromosome malsegregation to the daughter nuclei in cytokinesis-blocked transgenic mouse splenocytes. Chromosome Research, 3, 45-53.
6. CHEN, T. R., 1977, In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stain. Experimental Cell Research, 104, 255-262.
7. CRAIG, M. and BICKMORE, W. A., 1993, Chromosome bands - flavours to savour. BioEssays, 15, 349-354.
8. DUTRILLAUX, B., COUTURIER, J., VIEGAS-PÉQUIGNOT, E. and SCHAISON, G., 1977, Localization of chromatid breaks in Fanconi's anemia, using three consecutive strains. Human Genetics, 37, 65-71.
9. EVANS, H. J., NEARY, C. J. and WILLIAMSON, F. S., 1959, The relative biological efficiency of single doses of fast neutrons and gamma-rays on Vicia faba roots and the effect of oxygen. International Journal of Radiation Biology, 3, 216-229.
10. KANO, Y. and LITTLE, J. B., 1986, Site-specific chromosomal rearrangements induced in human diploid cells by x-irradiation. Cytogenetics and Cell Genetics, 41, 22-29.
11. KNEHR, S., ZITZELSBERGER, H., BRASELMANN, H. and BAUCHINGER, M., 1994, Analysis for DNA-proportional distribution of radiation-induced chromosome aberrations in various triple combinations of human chromosomes using fluorescence in situ hybridization. International Journal of Radiation Biology, 65, 683-690.
12. LAVIN, M. F., LE POIVEDIN, P. and BATES, P., 1992, Enhanced levels of radiation-induced G2 phase delay in ataxia telangiectasia heterozygotes. Cancer Genetics and Cytogenetics, 60, 183-187.
13. LEE, C. L. Y. and KAMRA, O. P., 1981, The pattern of radiation-induced transmissible aberrations in a human cell culture. Human Genetics, 57, 380-384.
14. LEFRANÇOIS, D., KOKALJ, N., VIEGAS-PÉQUIGNOT, E., MONTAGNIER, L. and DUTRILLAUX, B., 1991, High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives. Human Genetics, 86, 475-180.
15. LUCAS, J. N., AWA, A., STRAUME, T., POGGENSEE, M., KODAMA, Y., NAKANO, M., OHTAKI, K., WEIER, H-U., PINKEL., D., GRAY, J. and LITTLEFIELD, G., 1992, Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation. International Journal of Radiation Biology, 62, 53-63.
16. MILLER, B. M., WERNER, T., WEIER, H-U. and NÜSSE, M., 1993, Analysis of radiation-induced micronuclei by fluorescence in situ hybridization (FISH) simultaneously using telomeric and centromeric DNA probes. Radiation Research, 131, 177-185.
17. MORTON, N. E., 1991, Parameters of the human genome. Proceedings of the National Academy of Science, USA, 88, 7474-7476.
18. NEITZEL, H., 1986, A routine method for the establishment of permanent growing lymphoblastoid cell lines. Human Genetics, 73, 320-326.
19. NÜSSE, M., BEISKER, W., KRAMFR, J., MILLER, B. M., SCHREIBER, G. A., VIAGGI, S., WELLER, E. M. and WESSELS, J. M., 1994, Measurement of micronuclei by flow cytometry. In: Methods in Cell Biology. Edited by: Z. Darzynkiewcz, J. P. Robinson and H. A. Chrissman. (New York: Academic Press), Vol. 42, pp. 149-158.
20. SALASSIDIS, K., HUBER, R., ZITZELSBERGER, H. and BAUCHINGER, M., 1992, Centromere detection in vinblastine- and radiation-induced micronuclei of cytokinesis-blocked mouse cells by using in situ hybridization with a mouse gamma (major) satellite DNA probe. Environmental and Molecular Mutagenesis, 19, 1-6.
21. SASAKI, M. S. and TONOMURA, A., 1973, A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents. Cancer Research. 33, 1829-1836.
22. SAVAGE, J. R. K. and PAPWORTH, D. G., 1982, Frequency and distribution studies of asymmetrical versus symmetrical chromosome aberrations. Mutation Research, 95, 7-18.
23. SCHMID, E., ZITZELSBERGER, H., BRASELMANN, H., GRAY, J. W. and BAUCHINGER, M., 1992, Radiation-induced chromosome aberrations analysed by fluorescence in situ hybridization with a triple combination of composite whole chromosome-specific DNA probes. International Journal of Radiation Biology, 62, 673-678.
24. SLAVOTINEK, A., MILLER, E., TAYLOR, G. M., NÜSSE, M. and VAN HEYNINGEN, V., 1995, Micronucleus frequencies in lymphoblastoid cell lines measured with the cytokinesis-block technique and flow cytometry. Mutagenesis, 10, 439-445.
25. STRAUME, T. and LUCAS, J. N., 1993, A comparison of the yields of translocations and dicentrics measured using fluorescence in situ hybridization. International Journal of Radiation Biology, 64, 185-187.
26. SURRALLÉS, J., CARBONELL, E., MARCOS, R., DEGRASSI, F., ANTOCCIA, A. and TANZARELLA, C., 1992, A collaborative study on the improvement of the micronucleus test in cultured human lymphocytes. Mutagenesis, 7, 407-410.
27. TUCKER, J. D., RAMSEY, M. J., LEE, D. A. and MINKLER, J. L., 1993, Validation of chromosome painting as a biodosimeter in human peripheral lymphocytes following acute exposure to ionizing radiation in vitro. International Journal of Radiation Biology, 64, 27-37.
28. VIAGGI, S. BRASELMANN, H. and NÜSSE, M., 1995, Flow cytometric analysis of micronuclei in the CD2+-subpopulation of human lymphocytes enriched by magnetic separation. International Journal of Radiation Biology, 67, 193-202.
29. WEIER, H-U. G., LUCAS, J. N., POGGENSEE, M., SEGRAVES, R., PINKEL, D. and GRAY, J. W., 1991, Two-color hybridization with high complexity chromosome-specific probes and a degenerate alpha satellite probe DNA allows unambiguous discrimination between symmetrical and asymmetrical translocations. Chromosoma, 100, 371-376.
30. WELLER, E. M., DIETRICH, I., VIAGGI, S., BEISKER, W. and NüSSE, M., 1993, Flow cytometric analysis of bromodeoxyuridine-induced micronuclei. Mutagenesis, 8, 437-444.
31. YUNIS, J. J. and SANCHEZ, O., 1975, The G-banded prophase chromosomes of man. Humangenetik, 27, 167-172.
32. ZIJNO, A., MAŔCON, F., LEOPARDI, P. and CREBELLI, R., 1994, Simultaneous detection of X-chromosome loss and non-disjunction in cytokinesis-blocked human lymphocytes by in situ hybridization with a centromeric DNA probe; implications for the human lymphocyte in vitro micronucleus assay using cytochalasin B. Mutagenesis, 9, 225-232.