A high yield of translocations parallels the high yield of sister chromatid exchanges in the CHO mutant EM9

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 398, Issue 1-2, 1998, Pages 67-73

  Dominguez I ^a   Daza, P ^a   Natarajan, A T ^b   Cortes F ^a  

^a UNIVERSITY OF SEVILLE   (Spain)

^b LEIDEN UNIVERSITY   (Netherlands)

Author keywords

EM9; Fluorescence in situ hybridization; Sister chromatid exchange

Indexed keywords

BROXURIDINE; MUTAGENIC AGENT;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL LINE; CELL MUTANT; CHEMICAL MUTAGENESIS; CHO CELL; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; DNA DAMAGE; FLUORESCENCE IN SITU HYBRIDIZATION; NONHUMAN; PRIORITY JOURNAL; SISTER CHROMATID EXCHANGE;

ANIMALS; BROMODEOXYURIDINE; CHO CELLS; CRICETINAE; IN SITU HYBRIDIZATION, FLUORESCENCE; MUTAGENS; MUTATION; SISTER CHROMATID EXCHANGE; TRANSLOCATION, GENETIC;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS;

EID: 0032574313     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0027-5107(97)00241-8     Document Type: Article

References (40)

1. Lichter P., Cremer T., Tang C.J., Watkins P.C., Manuelidis L., Ward D.C. Rapid detection of human chromosome 21 aberrations by in situ hybridization. Proc. Natl. Acad. Sci. USA. 85:1988;9664-9668.
2. Boei J.J.W.A., Natarajan A.T. Detection of chromosome malsegregation to the daughter nuclei in cytokinesis-blocked transgenic mouse splenocytes. Chromosome Res. 3:1995;45-53.
3. Pinkel D., Landegent J., Collins C., Fuscoe J., Seagraves R., Lucas J., Gray J. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc. Natl. Acad. Sci. USA. 85:1988;9138-9142.
4. Natarajan A.T., Vyas R.C., Darroudi F., Vermeulen S. Frequencies of X-ray-induced chromosome translocations in human peripheral lymphocytes as detected by in situ hybridization using chromosome-specific DNA libraries. Int. J. Radiat. Biol. 61:1992;199-203.
5. Natarajan A.T., Balajee A.S., Boei J.J.W.A., Chatterjee S., Darroudi F., Grigorova M., Noditi M., Oh H.J., Slijepcevic P., Vermeulen S. Recent developments in the assessment of chromosomal damage. Int. J. Radiat. Biol. 66:1994;615-623.
6. Balajee A.S., Domínguez I., Natarajan A.T. Construction of Chinese hamster chromosome specific DNA libraries and their use in the analysis of spontaneous chromosome rearrangements in different cell lines. Cytogenet. Cell Genet. 70:1995;95-101.
7. Y. Xiao, P. Slijepcevic, G. Arkesteijn, F. Darroudi, A.T. Natarajan, Development of DNA libraries specific for Chinese hamster chromosomes #3, 4, 9, 10, X and Y by DOP-PCR, Cytogenet. Cell Genet., (1997) in press.
8. Domínguez I., Boei J.J.W.A., Balajee A.S., Natarajan A.T. Analysis of radiation-induced chromosome aberrations in Chinese hamster cells by FISH using chromosome-specific DNA libraries. Int. J. Radiat. Biol. 70:1996;199-208.
9. Thompson L.H., Brookman K.W., Dillehay L.E., Carrano A.V., Mazrimas J.A., Mooney C.L., Minkler J.L. A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and a extraordinary baseline frequency of sister-chromatid exchange. Mutation Res. 95:1982;427-440.
10. Chaganti R.S.K., Schonberg S., German J. A manifold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. Proc. Natl. Acad. Sci. USA. 71:1974;4508-4512.
11. Shiraishi Y., Freeman A.I., Sandberg A.A. Increased sister chromatid exchange in bone marrow and blood cells from Bloom's syndrome. Cytogenet. Cell Genet. 17:1976;162-173.
12. Pinkel D., Thompson L.H., Gray J.W., Vanderlaan M. Measurement of sister chromatid exchanges at very low bromodeoxyuridine substitution levels using a monoclonal antibody in Chinese ovary cells. Cancer Res. 45:1985;5795-5798.
13. Piñero J., Cortés F. Abnormally high incidence of SCE in three successive cell cycles in the CHO mutant EM9 as detected by a three-way immunoperoxidase differential staining. Mutation Res. 292:1993;205-211.
14. J.H. Ray, J. German, The chromosome changes in Bloom's syndrome, Ataxia-telangiectasia syndrome, and Fanconi's anaemia, in: E. Francis, A. Arrighi, P.N. Rao (Eds.), Genes, Chromosomes and Neoplasia, Raven, New York, 1981, pp 351-378.
15. Perry P., Wolff S. New Giemsa method for the differential staining of sister chromatids. Nature. 251:1974;156-158.
16. Morgan W.F., Schwartz J.L., Murnane J.P., Wolff S. Effect of 3-aminobenzamide on sister chromatid exchange frequency in X-irradiated cells. Radiat. Res. 93:1983;567-571.
17. Lucas J.N., Awa A., Straume T., Poggensee M., Kodama Y., Nakano M., Ohthaki K., Weier H.U., Pinkel D., Gray J., Littlefield G. Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation. Int. J. Radiat. Biol. 62:1992;53-63.
18. Cortés F., Piñero J., Palitti F. Cytogenetic effects of inhibition of topoisomerase I and II activities in the CHO mutant EM9 and its parental line AA8. Mutation Res. 288:1993;281-289.
19. Willis A.E., Lindahl T. DNA ligase I deficiency in Bloom's syndrome. Nature. 325:1987;355-357.
20. Chan J.Y.H., Becker F.F., German J., Ray J.H. Altered DNA ligase I activity in Bloom's syndrome cells. Nature. 325:1987;357-359.
21. Ellis N.A., Groden J., Ye T.Z., Lennon D.J., Ciocci S., Proyetchera M., German J. The Bloom syndrome gene product is homologous to RecQ helicases. Cell. 83:1995;655-666.
22. Chan J.Y.H., Thompson L.H., Becker F.F. DNA-ligase activities appear normal in the CHO mutant EM9. Mutation Res. 131:1984;209-214.
23. La Belle M., Linn S., Thompson L.H. Apurinic/apyrimidinic endonuclease activities appear normal in the CHO-cell ethyl methanesulphonate sensitive mutant EM9. Mutation Res. 141:1984;41-44.
24. Ikejima M., Bohannon D., Gill D.M., Thompson L.H. Poly(ADP-ribose) metabolism appears normal in EM9, a mutagen-sensitive mutant of CHO cells. Mutation Res. 128:1984;213-220.
25. Thompson L.H., Brookman K.W., Jones N.J., Allen S.A., Carrano A.V. Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand-break repair and sister chromatid exchange. Mol. Cell Biol. 10:1990;6160-6171.
26. Caldecott K.W., Mckeown C.K., Tucker J.D., Ljungquist S., Thompson L.H. An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase II. Mol. Cell Biol. 14:1994;68-76.
27. Tomkinson A.E., Roberts E., Daly G., Totti N.F., Lindahl T. Three distinct DNA ligases in mammalian cells. J. Biol. Chem. 266:1991;21728-21735.
28. A.T. Natarajan, A.A. van Zeeland, T.S. Zwanenburg, Influence of inhibitors of poly(ADP)ribose polymerase on DNA repair, chromosomal aberrations and mutations, in: M. Miwa, O. Hayashi, S. Shall, M. Smulson, T. Sugumura (Eds.), ADP-ribosylation, DNA Repair and Cancer, Japan Scientific Societies Press, Tokyo, 1983, pp. 227-242.
29. Schmid E., Zitzelsberger H., Braselmann H., Gray J.W., Bauchinger M. Radiation-induced chromosome aberrations analysed by fluorescence in situ hybridization with a triple combination of composite whole chromosome-specific DNA probes. Int. J. Radiat. Biol. 62:1992;673-678.
30. Bauchinger M., Schmid E., Zitzelsberger H., Braselmann H., Nahrstedt U. Radiation-induced chromosome aberrations analysed by two-colour fluorescence in situ hybridization with composite whole chromosome-specific DNA probes and a pancentromeric DNA probe. Int. J. Radiat. Biol. 64:1993;179-184.
31. Tucker J.D., Ramsey M.J., Lee D.A., Minkler J.L. Validation of chromosome painting as a biodosimeter in human peripheral lymphocytes following acute exposure to ionizing radiation in vitro. Int. J. Radiat. Biol. 64:1993;27-37.
32. Straume T., Lucas J.N. A comparison of yields of translocations and dicentrics measured using fluorescence in situ hybridization. Int. J. Radiat. Biol. 64:1993;185-187.
33. Nakano M., Nakashima E., Pawel D.J., Kodama Y., Awa A. Frequency of reciprocal translocations and dicentrics induced in human blood lymphocytes by X-irradiation as determined by fluorescence in situ hybridization. Int. J. Radiat. Biol. 64:1993;565-569.
34. Boei J.J.W.A., Balajee A.S., De Boer P., Rens W., Aten J.A., Mullenders L.H.F., Natarajan A.T. Construction of mouse chromosome-specific DNA libraries and their use for the detection of X-ray-induced aberrations. Int. J. Radiat. Biol. 65:1994;583-590.
35. Hande M.P., Boei J.J.W.A., Granath F., Natarajan A.T. The induction and persistence of cytogenetic damage in mouse splenocytes following whole-body X-irradiation analyzed by fluorescence in situ hybridization: Dicentrics and translocations. Int. J. Radiat. Biol. 69:1996;437-446.
36. Natarajan A.T., Balajee A.S., Boei J.J.W.A., Darroudi F., Domínguez I., Hande M.P., Meijers M., Slijepcevic P., Vermeulen S., Xiao Y. Mechanisms of induction of chromosome aberrations and their detection by fluorescence in situ hybridization. Mutation Res. 372:1996;247-258.
37. Therman E., Kuhn E.M. Mitotic crossing over and segregation in man. Hum. Genet. 59:1981;92-100.
38. Sakamoto Hojo E.T., van Diemen P.C.M., Darroudi F., Natarajan A.T. Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridization (FISH) technique. Mutation Res. 334:1995;59-69.
39. L.H. Thompson, Mammalian cell mutations affecting recombination, in: R. Kucherlapati, G.R. Smith (Eds.), Genetic Recombination, ASM, Washington, DC, 1988, pp. 597-620.
40. Natarajan A.T., Csukás I., van Zeeland A.A. Contribution of incorporated 5-bromodeoxyuridine in DNA to the frequencies of sister-chromatid exchanges induced by inhibitors of poly-(ADP-ribose)-polymerase. Mutation Res. 84:1981;125-132.