Use of Restriction Endonucleases to Study Relationships between DNA Double-strand Breaks, Chromosomal Aberrations and Other End-points in Mammalian Cells

References

• Ahnstrom G., Erixon K. Radiation-induced strand breakage in DNA from mammalian cells: strand separation in alkaline solution. International Journal of Radiation Biology 1973; 23: 285–289
   Web of Science ®Google Scholar
• Barendsen G.W., Walter H.M.D. Effects of different ionizing radiations on human cells in tissue culture. Radiation Research 1964; 21: 314–329
   PubMed Web of Science ®Google Scholar
• Barnes G., Rine J. Regulated expression of the endonuclease Eco R1 in Saccharomyces cerevisiae: nuclear entry and biological consequences. Proceedings of the National Academy of Sciences, U.S.A., 82: 1354–1358
   Google Scholar
• Bender M.A., Griggs H.G., Bedford J.S. Mechanisms of chromosomal aberration production. III: Chemicals and ionizing radiation. Mutation Research 1974; 23: 197–212
   PubMed Web of Science ®Google Scholar
• Bishop D.T., Williamson J.A., Skolnick M.H. A model for restriction fragment length distributions. American Journal of Human Genetics 1983; 35: 795–815
   PubMed Web of Science ®Google Scholar
• Bloecher D. DNA double-strand breaks in Ehrlich ascites tumour cells at low doses of X-rays. I. Determination of induced breaks by centrifugation at low speed. International Journal of Radiation Biology 1982; 42: 317–328
   Web of Science ®Google Scholar
• Bloecher D., Pohlit W. DNA double-strand breaks in Ehrlich ascites tumour cells at low doses of X-rays II. Can cell death be attributed to double-strand breaks?. International Journal of Radiation Biology 1982; 42: 329–338
   Google Scholar
• Bryant P.E. Enzymatic restriction of mammalian cell DNA using Pvu II and Bam H1: evidence for the double-strand break origin of chromosomal aberrations. International Journal of Radiation Biology 1984; 46: 57–65
   Web of Science ®Google Scholar
• Bryant P.E. Enzymatic restriction of mammalian cell DNA: evidence for double-strand breaks as potentially lethal lesions. International Journal of Radiation Biology 1985; 48: 55–60
   Web of Science ®Google Scholar
• Bryant P.E., Bloecher D. Measurement of the kinetics of DNA double-strand break repair in Ehrlich ascites tumour cells using the unwinding method. International Journal of Radiation Biology 1980; 38: 335–347
   Web of Science ®Google Scholar
• Bryant P.E., Birch D., Jeggo P.A. High chromosomal sensitivity of Chinese hamster xrs 5 cells to restriction endonuclease induced double-strand breaks. International Journal of Radiation Biology 1987; 52: 537–554
   Web of Science ®Google Scholar
• Carrano A.V. Chromosomal aberrations and radiation-induced cell death, II. Predicted and observed cell survival. Mutation Research 1973; 17: 355–357
   PubMed Web of Science ®Google Scholar
• Celis J.E. Microinjection of somatic cells with micropipettes: comparison with other transfer techniques. Biochemical Journal 1984; 223: 281–291
   PubMed Web of Science ®Google Scholar
• Cook P.R., Brazell I. Determination and repair of single-strand breaks in nuclear DNA. Nature 1975; 263: 679–682
   Google Scholar
• Coquerelle T., Bopp A., Kesseler B., Hagen U. Strand breaks and 5′ end groups in DNA of irradiated thymocytes. International Journal of Radiation Biology 1973; 24: 397–404
   Web of Science ®Google Scholar
• Corry P.M., Cole A. Double-strand rejoining in mammalian cells. Nature New Biology 1973; 245: 100–101
   PubMedGoogle Scholar
• Costa N.A., Bryant P.E. Repair of single-strand and double-strand breaks in the Chinese hamster xrs 5 mutant cell line as determinted by DNA unwinding. Mutation Research: DNA Repair Reports 1988, in the press
   Google Scholar
• Cox R., Debenham P.G., Masson W.K., Webb M.B.T. Ataxia telagiectasia: a human mutation giving high-frequency misrepair of DNA double-strand scissions. Molecular Biology in Medicine 1986; 3: 229–244
   PubMedGoogle Scholar
• Darroudi F., Natarajan A.T. Cytological characterization of Chinese hamster ovary X-ray sensitive mutants xrs 5 and xrs 6. I: Induction of chromosomal aberrations by X-irradiation and its modulation with 3-amino benzamide and caffeine. Mutation Research 1987; 177: 133–148
   PubMed Web of Science ®Google Scholar
• Evans H.J. Molecular mechanisms in the induction of chromosomal aberrations. Progress on Genetic Toxicology, D. Scott, B.A. Bridges, F.H. Sobels. Elsevier/North-Holland Biomedical Press, Amsterdam 1977; 57–74
   Google Scholar
• Fonck K., Barthel R., Bryant P.E. Kinetics of recombinational hybrid formation in X-irradiated mammalian cells: a possible first step in the repair of DNA double-strand breaks. Mutation Research: DNA Repair Reports 1984; 132: 113–118
   Google Scholar
• Frankenberg-Schwager M., Frankenberg D., Bloecher D., Adamczyk C. Repair of DNA double-strand breaks in irradiated yeast under non-growth conditions. Radiation Research 1980; 82: 498–510
   PubMed Web of Science ®Google Scholar
• Green M.H.L., Lowe J.E. Failure to detect a repair-related defect in the transfection of ataxia-telangiectasia cells by an enzymatically restricted plasmid. International Journal of Radiation Biology 1987; 52: 437–446
   Web of Science ®Google Scholar
• Gustavino B., Johannes C., Obe G. Restriction endonuclease Bam H1 induces chromosomal aberrations in Chinese hamster ovary (CHO) cells. Mutation Research 1986; 175: 91–95
   PubMed Web of Science ®Google Scholar
• Halford S.E. How does Eco R1 cleave its recognition site on DNA?. Trends in Biochemical Sciences 1983; 8: 455–460
   Google Scholar
• Henner W.D., Grunberg S.M., Haseltine W.A. Sites and structure of gamma radiation induced DNA strand breaks. Journal of Biological Chemistry 1982; 257: 11750–11754
   PubMed Web of Science ®Google Scholar
• Ho K.Y. Induction of DNA double-strand breaks by X-rays in a radioresistant strain of the yeast Saccharomyces cereviseae. Mutation Research 1975; 30: 327–334
   PubMed Web of Science ®Google Scholar
• Houck C.M., Reinhart F.P., Schmid C.W. A ubiquitous family of repeated DNA sequences in the human genome. Journal of Molecular Biology 1979; 132: 289–306
   PubMed Web of Science ®Google Scholar
• Jeggo P.A., Kemp L.M. X-ray sensitive mutants of Chinese hamster ovary cell line: isolation and cross-sensitivity to other DNA damaging agents. Mutation Research 1983; 112: 313–327
   PubMed Web of Science ®Google Scholar
• Jeggo P.A., Kemp L.M., Holliday R. The application of the microbial ‘tooth-pick’ technique to somatic cell genetics, and its use in the isolation of X-ray sensitive mutants of Chinese hamster ovary cells. Biochemie 1983; 64: 713–715
   Google Scholar
• Joshi G.P., Nelson W.J., Revell S.H., Shaw C.A. X-ray induced chromosome damage in live mammalian cells, an improved measurement of its effect on their colony forming ability. International Journal of Radiation Biology 1982; 41: 161–181
   Web of Science ®Google Scholar
• Kaebling M., Miller D.A., Miller O.J. Restriction enzyme banding of mouse metaphase chromosomes. Chromosoma 1984; 90: 128–132
   Google Scholar
• Kemp L.M., Jeggo P.A. Radiation-induced chromosome damage in X-ray-sensitive mutants (xrs) of the Chinese hamster ovary cell line. Mutation Research: DNA Repair Reports 1986; 166: 255–263
   PubMedGoogle Scholar
• Kemp L.M., Sedgewick S.G., Jeggo P.A. X-ray sensitive mutants of Chinese hamster ovary cells defective in double-strand break rejoining. Mutation Research 1984; 132: 189–196
   PubMed Web of Science ®Google Scholar
• Krasin F., Hutchinson F. Repair of DNA double-strand breaks in Escherichia coli which requires rec A function in the presence of a duplicate genome. Journal of Molecular Biology 1977; 116: 81–98
   PubMed Web of Science ®Google Scholar
• Lamb J.F., Ogden P.H. Transient changes in permeability in HeLa and L cells during detachment from a substrate. Quarterly Journal of Experimental Physiology 1987; 72: 189–199
   Google Scholar
• Lederberg S., Meselson M. Degradation of non-replicating bacteriophage DNA in non-accepting cells. Journal of Molecular Biology 1964; 8: 623–628
   PubMed Web of Science ®Google Scholar
• Lehmann A.R., Stevens S. The production and repair of double-strand breaks in cells from normal humans and from patients with ataxia telangiectasia. Biochemica et Biophysica Acta 1977; 474: 49–60
   PubMed Web of Science ®Google Scholar
• Lennartz M., Coquerelle T., Hagen U. Modification of end groups in DNA strand breaks of irradiated thymocytes during early repair. International Journal of Radiation Biology 1975; 28: 181–185
   Web of Science ®Google Scholar
• Malone J.F., Foster C.J. The effect of hypertonic shock on the radiation response of HeLa-3 cells. International Journal of Radiation Biology 1972; 22: 599–605
   Web of Science ®Google Scholar
• McNeil P.L., Murphy R.F., Launi F., Taylor D.L. A method of incorporating macromolecules into adherent cells. Journal of Cell Biology 1984; 98: 1556–1564
   PubMed Web of Science ®Google Scholar
• Modrich P. Structures and mechanisms of DNA restriction and modifying enzymes. Quarterly Review of Biophysics 1979; 12: 315–369
   PubMed Web of Science ®Google Scholar
• Moore P.D., Song K.Y., Chekuri L., Wallace L., Kuchelapati R.S. Homologous recombination in a Chinese hamster X-ray sensitive mutant. Mutation Research 1987; 160: 149–155
   Google Scholar
• Munro T.R. Effects of hypertonic sucrose on the radiosensitivity of Chinese hamster fibroblasts. British Journal of Radiology 1969; 42: 784–786
   PubMed Web of Science ®Google Scholar
• Natarajan A.T., Obe G. Molecular mechanisms involved in the production of chromosomal aberrations. Chromosoma 1984; 90: 120–127
   PubMed Web of Science ®Google Scholar
• Natarajan A.T., Obe G., van Zeeland A.A., Palitti F., Meijers M., Verdegaal-Immerzell E.A.M. Molecular mechanisms involved in the production of chromosomal aberrations; II. Utilization of Neurospora endonuclease for the study of aberration production by X-rays in G1 and G2 stages of the cell cycle. Mutation Research 1980; 69: 293–305
   PubMed Web of Science ®Google Scholar
• Natarajan A.T., Mullenders L.H.F., Meijers M., Mukherjee M. Induction of sister chromatid exchanges by restriction endonucleases. Mutation Research 1985; 144: 33–39
   PubMedGoogle Scholar
• Obe G., Johannes C. Chromosomal aberrations induced by the restriction endonuclease Alu I and Bam H1: comparison with X-rays. Biologisches Zentral Blatt 1987; 106: 175–190
   Google Scholar
• Obe G., Kamra O.P. Elevation of Alu I-induced frequencies of chromosomal aberrations in Chinese hamster ovary cells by Neurospora crassa endonuclease and by ammonium sulphate. Mutation Research 1986; 174: 34–36
   Google Scholar
• Obe G., Natarajan A.T. Comparison between inactivated Sendai virus, polyethylene glycol, and Tween 80 as permeabilizing agents for introducing Neurospora endonuclease into X-irradiated cells. Mutation Research 1980; 71: 133–138
   Google Scholar
• Obe G., Natarajan A.T. Chromosomal aberrations induced by the restriction endonuclease Alu I in Chinese hamster cells: influence of duration of treatment and potentiation by cytosine arabinoside. Mutation Research 1985; 152: 205–210
   PubMed Web of Science ®Google Scholar
• Obe G., Winkel E.U. The chromosome breaking activity of the restriction endonuclease Alu I in CHO cells is independent of the S-phase of the cell cycle. Mutation Research 1985; 152: 25–29
   PubMed Web of Science ®Google Scholar
• Obe G., Jonas R., Schmidt S. The restriction endonuclease Alu I induces chromosomal aberrations in human peripheral lymphocytes in vitro. Mutation Research 1987; 163: 271–275
   Google Scholar
• Obe G., Palitti F., Tanzarella C., Degrassi F., DeSalvia R. Chromosomal aberrations induced by restriction endonucleases. Mutation Research 1985; 150: 359–368
   PubMed Web of Science ®Google Scholar
• Obe G., Von der Hude W., Scheutwinkel-Reich M., Baseler A. The restriction endonuclease Alu I induces chromosomal aberrations and mutations in the hypoxanthine phosphoribosyl transferase locus but not in the Na+/K+ ATPase locus in V79 hamster cells. Mutation Research 1986; 174: 71–74
   PubMedGoogle Scholar
• Okada C.Y., Rechsteiner M. Introduction of macromolecules into cultured mammalian cells by osmolytic lysis of pinocytic vesicles. Cell 1982; 29: 33–41
   PubMed Web of Science ®Google Scholar
• Perry P., Evans H.J. Cytological detection of mutagen-carcinogen exposure by sister chromatid exchange. Nature (London) 1975; 258: 121–125
   PubMed Web of Science ®Google Scholar
• Preston R.J. The effect of cytosine arabinoside on the frequency of X-ray-induced chromosomal aberrations in normal human leukocytes. Mutation Research 1980; 69: 71–79
   PubMed Web of Science ®Google Scholar
• Preston R.J. The use of inhibitors of DNA repair in the study of mechanisms of chromosomal aberrations. Cytogenetics and Cell Genetics 1982; 33: 20–26
   Google Scholar
• Raaphorst G.P., Dewey W.C. Alterations in the radiosensitivity of CHO cells by anisotonic treatments: correlations between cell lethality and chromosomal aberrations. Radiation Research 1979; 79: 403–416
   PubMed Web of Science ®Google Scholar
• Resnick M.A. The repair of double-strand breaks in DNA: A model involving recombination. Journal of Theoretical Biology 1976; 59: 97–106
   PubMed Web of Science ®Google Scholar
• Roberts R.J. Restriction enzymes and their isoschizomers. Nucleic Acids Research 1987; 15: 189–217
   Google Scholar
• Schlegel R.A., Rechsteiner M.C. Microinjection of thymidine kinase and bovine serum albumin into mammalian cells by fusion with red blood cells. Cell 1975; 5: 371–379
   PubMed Web of Science ®Google Scholar
• Stoilov L., Mullenders L.H.F., Natarajan A.T. Influence of bromodeoxyuridine substitution of thymidine on sister-chromatid exchanges and chromosomal aberrations induced by restriction endonucleases. Mutation Research 1986; 174: 295–301
   PubMed Web of Science ®Google Scholar
• Subrahmanyan N.C., Gould A.R., Doy C.H. Cleavage of plant chromosomes by restriction endonucleases. Plant Science Letters 1976; 6: 203–208
   Google Scholar
• Tanaka K., Sekiguchi M., Okada Y. Restoration of ultraviolet-induced unscheduled DNA synthesis of xeroderma pigmentosum cells by the concomitant treatment with bacteriophage T4 endonuclease V and HVJ (Sendai virus). Proceedings of the National Academy of Sciences, U.S.A. 1975; 72: 4071–4075
   PubMed Web of Science ®Google Scholar
• Taylor A.M.R. Unrepaired DNA strand breaks in irradiated ataxia telangiectasia lymphocytes suggested from cytogenetic observations. Mutation Research 1978; 50: 407–418
   PubMed Web of Science ®Google Scholar
• Thacker J. The use of recombinant DNA techniques to study radiation induced damage, repair and genetic change in mammalian cells. International Journal of Radiation Biology 1986; 50: 1–30
   Web of Science ®Google Scholar
• Utsumi H., Elkind M.M. Potentially lethal damage versus sublethal damage: independent repair processes in actively growing Chinese hamster cells. Radiation Research 1979; 77: 346–360
   PubMed Web of Science ®Google Scholar
• Vasudev V., Obe G. Evidence for a receptor mediated endocytosis of Alu I in Chinese hamster ovary cells. Mutation Research 1988; 197: 109–116
   Google Scholar
• Wineger R.A., Preston R.J. The induction of chromosomal aberrations by restriction endonucleases that produce blunt-ended or cohesive-ended double-strand breaks. Mutation Research 1988; 197: 141–149
   Google Scholar
• Zajac-Kaye M., T'so P.O. DNAase I encapsulated in liposomes can induce neoplastic transformation of Syrian hamster embryo cells in culture. Cell 1984; 39: 427–437
   PubMedGoogle Scholar
• Zhang S., Dong W. Chromosomal aberrations induced by the restriction endonucleases Eco R1, Pst I, Sal I, and Bam H1 in CHO cells. Mutation Research 1987; 180: 109–114
   PubMedGoogle Scholar