Investigating the nature of chromatid breaks produced by restriction endonucleases

References

• BRYANT, P. E., 1984, Enzymatic restriction of mammalian cell DNA using Pvull and Barn HI: evidence for the double-strand break origin of chromosomal aberrations. Inter-national Journal of Radiation Biology, 46, 57–65.
   Web of Science ®Google Scholar
• BRYANT, P. E. and CHRISTIE, A. F., 1989, Induction of chromosomal aberrations in CHO cells by restriction endonucleases: effects of blunt- and cohesive-ended double-strand breaks in cells treated by the 'pellet' method. Mutation Research, 213, 233–241.
   PubMed Web of Science ®Google Scholar
• CHADWICK, K. H. and LEENHOUTS, H. P., 1981, The Molecular Theory of Radiation Biology, (Berlin: Springer).
   Google Scholar
• COSTA, N. D., MASSON, W. K. and THACKER, J., 1993, The effec-tiveness of restriction endonucleases in cell killing and mutation. Somatic Cell and Molecular Genetics, 19, 479–490.
   PubMedGoogle Scholar
• GOODHEAD, D. G., THACKER, J. and Cox, R., 1993, Effects of radiations of different qualities on cells: molecular mechanisms of damage and repair. InternationalJournal of Radiation Biology, 63, 543–556.
   PubMed Web of Science ®Google Scholar
• GRIFFIN, C. S., HARVEY, A. N. and SAVAGE, J. R. K., 1994, Chromatid damage induced by 238Pu a-particles in G2 and S phase Chinese hamster V79 cells. International Journal of Radiation Biology, 66, 85–98.
   PubMed Web of Science ®Google Scholar
• HARVEY, A. N., COSTA, N. D., THACKER, J. and SAVAGE, J. R. K., Chromosomal aberrations induced by defined DNA double strand breaks: the origin of achromatic lesions. Cancer Research (submitted).
   Google Scholar
• HARVEY, A. N. and SAVAGE, J. R. K., 1992, Simple cell-cycle analysis in second division cells. Clinical Cytogenetics Bulletin, 2, 94–96.
   Google Scholar
• HEDDLE, J. A., WHISSELL, D. and BODYCOTE, H. J., 1969, Changes in chromosome structure induced by radiations: a test of the two chief hypotheses. Nature, 221, 1158–1160.
   PubMedGoogle Scholar
• LEA, D. E., 1946, Actions of Radiations on Living Cells. (Cam-bridge: Cambridge University Press).
   Google Scholar
• NATARAJAN, A. T. and OBE, G., 1984, Molecular mechanisms involved in the production of chromosomal aberra-tions: III. Restriction endonucleases. Chromosoma, 90, 120–127.
   PubMed Web of Science ®Google Scholar
• NICOLAIDES, N. C. and STOECKERT, C. J., 1990, A simple, efficient method for the separate isolation of RNA and DNA from the same cells. Biotechniques, 8, 154–156.
   PubMedGoogle Scholar
• OBE, G., JOHANNES, C. J. and SCHULTE-FROHLINDE, D., 1992, DNA double-strand breaks induced by sparsely ionizing radi-ation and endonucleases as critical lesions for cell death, chromosomal aberrations, mutations and onco-genic transformation. Mutagenesis, 7, 3–12.
   Google Scholar
• PERRY, P. E. and WOLFF, S., 1974, New Giemsa method for the differential staining of sister chromatids. Nature, 251, 156–158.
   PubMed Web of Science ®Google Scholar
• REVELL, S. H., 1955, A new hypothesis for 'chromatid' changes. In Proceedings of a Biology Symposium (1954, Liege), edited by Z. M. Bacq and P. Alexander (London: Butter-worths) pp. 84–94.
   Google Scholar
• REVELL, S. H., 1959, The accurate estimation of chromatid breakage and its relevance to a new interpretation of chromatid aberrations induced by ionising radiations. Proceedings of the Royal Society (London), Series B, 150, 563–589.
   PubMed Web of Science ®Google Scholar
• REVELL, S. H., 1974, The breakage-and-reunion theory and the exchange theory for chromosomal aberrations induced by ionising radiations: a short history. Advances in Radiation Biology, 4, 367–416.
   Google Scholar
• SAVAGE, J. R. K., 1976, Annotation: Classification and relation-ships of induced chromosomal structural changes. Journal of Medical Genetics, 13, 103–122.
   PubMed Web of Science ®Google Scholar
• SAVAGE, J. R. K., 1986, The 'Revell Loop'. Clinical Cytogenetics Bulletin, 1, 192–196.
   Google Scholar
• SAVAGE, J. R. K., 1989, The production of chromosome struc-tural changes by radiation: an update of Lea (1946), chapter VI. British Journal of Radiology, 62, 507–520.
   PubMed Web of Science ®Google Scholar
• SAVAGE, J. R. K. and HARVEY, A. N., 1991, Revell revisited. Mutation Research, 250, 307–317.
   Google Scholar
• SAVAGE, J. R. K. and HARVEY, A. N., 1994, Investigations of aberration origins using BrdU. In Chromosomal Aberra-tions: Origin and Significance, edited by G. Obe and A. T. Natarajan (Berlin: Springer) pp. 76–91.
   Google Scholar
• SAVAGE, J. R. K. and PAPWORTH, D. G., 1991, Excogitations about the quantification of structural chromosomal aberra-tions. In Advances in Mutagenesis Research, 3, edited by G. Obe (Berlin: Springer), pp. 162–189.
   Google Scholar
• SAVAGE, J. R. K., PRESTON, R. J. and NEARY, G. J., 1968, Chromatid Aberrations in Tradescantia bracteata and a further test of Revell's Hypothesis. Mutation Research, 5, 47–56.
   Google Scholar
• SAX, K., 1940, An analysis of X-ray-induced chromosomal aberrations in Tradescantia. Genetics, 25, 41–68.
   PubMedGoogle Scholar
• SAX, K., 1941, Types and frequencies of chromosomal aberra-tions induced by X-rays. Cold Spring Harbour Symposium Quantitative Biology, 9, 93–103.
   Google Scholar
• WOLFF, S. and PERRY, P., 1974, Differential Giemsa staining of sister-chromatids and the study of sister-chromatid exchanges without auto radiography. Chromosoma, 48, 341–353.
   PubMed Web of Science ®Google Scholar
• WOLFF, S. and BODYCOTE, J. D., 1975, The induction of chro-matid deletions in accordance with the breakage-and-reunion hypothesis. Mutation Research, 29, 85–91.
   PubMedGoogle Scholar