5
Views
6
CrossRef citations to date
0
Altmetric
Original Article

Functional Complementation Studies with X-ray-sensitive Mutants of Chinese Hamster Cells Closely Resembling Ataxia-telangiectasia Cells

, , , , &
Pages S189-S195 | Received 22 May 1994, Accepted 10 Jul 1994, Published online: 03 Jul 2009

References

  • Collins A. Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics. Mutation Research 1993; 293: 99–118
  • Gatti R.A. Localizing the genes for ataxia-telangiectasia: a human model for inherited cancer susceptibility. Advances in Cancer Research 1991; 56: 77–104
  • Graham F.L., van der Eb A. A new technique for the assay of infectivity of human adenovirus 5 DNA. Journal of Virology 1973; 52: 456–467
  • Jaspers N.G.J., Gatti R.A., Baan C., Linssen P.C., Bootsma D. Genetic complementation analysis of ataxia-telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients. Cytogenetics and Cell Genetenetics 1988; 49: 259–263
  • Jones N.J., Stewart S.A., Thompson L.H. Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia-telangiectasia cells. Mutagenesis 1990; 5: 15–23
  • Jongmans W., Verhaegh G.W.C.T., Sankaranarayanan K., Lohman P.H.M., Zdzienicka M.Z. Cellular characteristics of A-T-like V79 cell mutants. Mutation Research 1993a; 294: 207–214
  • Jongmans W., Wiegant J., Oshimura M., James M.R., Lohman P.H.M., Zdzienicka M.Z. Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in A-T-like Chinese hamster cell mutants. Human Genetics 1993b; 92: 259–264
  • Kapp L.N., Painter R.B. Stable radioresistance in ataxia-telangiectasia cells containing DNA from normal human cells. International Journal of Radiation Biology 1989; 56: 667–675
  • Kapp L.N., Painter R.B., Yu L.-C., van Loon N., Richard C.W., III, James M.R., Cox D.R., Murname J.P. Cloning of a candidate gene for ataxia-telangiectasia group D. American Journal of Human Genetics 1992; 51: 45–54
  • Koi M., Shimizu M., Morita H., Yamada H., Oshimura M. Construction of mouse A9 clones containing a single human chromosome tagged with neoresistance gene via microcell fusion. Japanese Journal of Cancer Research 1989; 80: 413–418
  • Komatsu K., Okumura Y., Kodama S., Yoshida M., Miller R.C. Lack of correlation between radio-sensitivity and inhibition of DNA synthesis in hybrids (A-T × HeLa). International Journal of Radiation Biology 1989; 56: 863–867
  • Lambert C., Sschultz R.A., Smith M., Wagner-McPherson C., McDaniel L.D., Donolon T., Stanbridge E.J., Friedberg E.C. Functional complementation of ataxia-telangiectasia group D (A-T-D) cells by microcell-mediated chromosome transfer and mapping of the A-T-D locus to the region 11q22-23. Proceedings of the National Academy of Sciences, USA 1991; 88: 5907–5911
  • Lavin M.F., Schroeder A.L. Damage-resistant DNA synthesis in eukaryotes. Mutation Research 1988; 193: 193–206
  • Lehmann A.R., Arlett C.F., Burke J.F., Green M.H., James M.R., Lowe J.E. A derivative of an ataxia-telaniectasia (A-T) cell line with normal radio-sensitivity but A-T-like inhibition of DNA synthesis. International Journal of Radiation Biology 1986; 49: 639–643
  • McKinnon P.J. Ataxia-telangiectasia: an inherited disorder of ionizing-radiation sensitivity in man. Progress in the elucidation of the underlying biochemical defect. Human Genetics 1987; 75: 197–208
  • Meyn M.S., Lu-Kuo J.M., Herzing L.B.K. Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts. American Journal of Human Genetics 1993; 53: 1206–1216
  • Painter R.B., Young B.R. Radiosensitivity in ataxia-telangiectasia: A new explanation. Proceedings of the National Academy of Sciences, USA 1980; 77: 7315–7317
  • Sambrook J., Fritsch E.F., Maniatis T. Molecular Cloning; a Laboratory Manual2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor 1989
  • Sedgwick R.P., Boder E. Ataxia-telangiectasia. Hereditary Neuropathies and Spinocerebellar Atrophies, J.M.B.V. De Jong. Handbook of Clinical Neurology, Elsevier, Amsterdam 1991; 347–423, Vol 16, (60)
  • Thacker J., Ganesh A.N. DNA-break repair, radioresistance of DNA synthesis, and camptothecin sensitivity in the radiation-sensitive irs mutant: comparisons to ataxia-telangiectasia cells. Mutation Research 1990; 235: 49–58
  • Verhaegh G.W.C.T., Jaspers N.G.J., Lohman P.H.M., Zdzienicka M.Z. Co-dominance of radioresistant DNA synthesis in a group of A-T-like Chinese hamster cell mutants. Cytogenetics and Cell Genetics 1993; 63: 176–180
  • Weeda G., Hoeijmakers J.H.J. Genetic analysis of nucleotide excision repair in mammalian cells. Cancer Biology 1993; 4: 105–117
  • Wiegant J., Ried T., Nederlof P.M., Ploeg M., van der Taneke H.J., Raap A.K. In situ hybridization with fluoresceinated DNA. Nucleic Acids Research 1991; 19: 3237–3241
  • Zdzienicka M.Z., Jaspers N.G.J., van der Schans G.P., Natarajan A.T., Simons J.W.I.M. Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair. Cancer Research 1989; 49: 1481–1485
  • Zdzienicka M.Z., Simons J.W.I.M. Mutagensensitive cell lines are obtained with a high frequency in V79 Chinese hamster cells. Mutation Research 1987; 178: 235–244
  • Ziv Y., Danieli T., Rotman G., Sartiel A., Bar-Shira A., Jaspers N.G.J., Swirski R., Schimke R.T., Eddy R.L., Shows T.B., Shiloh Y. Ataxia-telangiectasia, R.A. Gatti, R.B. Painter. NATO ASI Series, Springer, Berlin 1993; H77: 65–74

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.