Repair of Potentially Lethal Damage by Introduction of T4 DNA Ligase in Eucaryotic Cells

References

• Belli J.A., Sheldon M. Potentially lethal radiation damage: repair by mammalian cells in culture. Science 1969; 165: 490–492
   PubMed Web of Science ®Google Scholar
• Bryant P.E. Enzymatic restriction of mammalian cell DNA using PvuII and BamH1: 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. Use of restriction endonucleases to study relationships between DNA double-strand breaks, chromosomal aberrations and other end-points in mammalian cells. International Journal of Radiation Biology 1988; 54: 869–890
   PubMed Web of Science ®Google Scholar
• Chadwick K.H., Leenhouts H.P. The Molecular Theory of Radiation Biology. Springer-Verlag, Berlin 1981; 168–168
   Google Scholar
• Chan J.Y.H., Becker F.F., German J., Ray J.H. Altered DNA ligase I activity in Bloom's syndrome cells. Nature 1987; 325: 357–359
   PubMed Web of Science ®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
• Gustavino B., Johannes C., Obe G. Restriction endonuclease BamH1 induces chromosomal aberrations in Chinese hamster ovary (CHO) cells. Mutation Research 1986; 175: 91–95
   PubMed Web of Science ®Google Scholar
• Heitman J., Zinder N.D., Model P. Repair of the Escherichia Coli chromosome after in vivo scission by the EcoRI endonuclease. Proceedings of the National Academy of Sciences, USA 1989; 86: 2281–2285
   PubMed Web of Science ®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
• 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
• Iliakis G. Radiation-induced potentially lethal damage: DNA lesions susceptible to fixation. International Journal of Radiation Biology 1988; 53: 541–584
   Web of Science ®Google Scholar
• Jacobs A., Bopp A., Hagen U. In vitro repair of single-strand breaks in gamma-irradiated DNA by polynucleotide ligase. International Journal of Radiation Biology 1972; 22: 431–435
   Web of Science ®Google Scholar
• Lehman I.R. DNA ligase: structure, mechanism, and function. Science 1974; 186: 790–797
   PubMed Web of Science ®Google Scholar
• Little J.B. Repair of PLD in mammalian cells: enhancement by conditioned medium from stationary cultures. International Journal of Radiation Biology 1971; 20: 87–92
   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
• Obe G., Natarajan A.T. Chromosomal aberrations induced by the restriction endonuclease AluI 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
• Okada C.Y., Rechsteiner M. Introduction of macromolecules into cultured mammalian cells by osmotic lysis of pinocytic vesicles. Cell 1982; 29: 33–41
   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
• Reznikoff C.A., Brankow D.W., Heidelberger C. Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division. Cancer Research 1973; 33: 3231–3238
   PubMed Web of Science ®Google Scholar
• Sgaramella V., Van de Sande J.H., Khorana H.G. Studies on polynucleotides, C. A novel joining reaction catalyzed by the T4-polynucleotide ligase. Proceedings of the National Academy of Sciences, USA, 1970; 1468–1475, 67
   Google Scholar
• Söderhäll S., Lindahl T. DNA ligases in eucaryotes. FEBS 1976; 67: 1–8
   PubMed Web of Science ®Google Scholar
• Szostak J., Orr-Weaver T., Rothstein R., Stahl F. The double-strand break repair model for recombination. Cell 1983; 33: 25–35
   PubMed Web of Science ®Google Scholar
• Tuschy S., Obe G. Potentiation of AluI-induced chromosome aberrations by high salt concentration in Chinese hamster ovary cells. Mutation Research 1988; 207: 83–87
   PubMed Web of Science ®Google Scholar
• Vernooij B., Hood L. The quality of T4 DNA ligase. Focus 1989; 11: 28–29
   Google Scholar
• Whitmore G.F., Guyas S. Studies on recovery process in mouse cells. National Cancer Institute Monographs 1967; 24: 141–156
   PubMedGoogle Scholar
• Willis A.E., Lindahl T. DNA ligase I deficiency in Bloom's syndrome. Nature 1987; 325: 355–357
   PubMed Web of Science ®Google Scholar
• Winegar 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
   PubMed Web of Science ®Google Scholar
• Winegar R.A., Phillips J.W., Youngblom J.H., Morgan W.F. Cell electroporation is a highly efficient method for introducing restriction endonucleases into cells. Mutation Research 1989; 225: 49–53
   PubMed Web of Science ®Google Scholar
• Yang T.C., Craise L.M., Mei M., Tobias C.A. Neoplastic cell transformation by high-LET radiation: molecular mechanisms. Advances in Space Research 1989; 9: 131–140
   PubMedGoogle Scholar