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Complementation of the Cellular A-T Phenotype by Gene Transfer

  • Conference paper
Ataxia-Telangiectasia

Abstract

The identification of the genes responsible for the chromosomal breakage syndromes by their function has been discussed since the discovery of the common feature of these diseases, cellular sensitivity to specific DNA damaging agents. The advent of gene transfer methods supplied the experimental system for this approach, which is apparently simple and straightforward: Exogenous DNA is introduced in vitro into the patient’s cells, and selection is applied to identify cell clones showing increased resistance to the lethal action of the DNA damaging agent. An attempt is then made to rescue the piece of DNA responsible for this phenotypic change, which is expected to represent a candidate gene.

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© 1993 Springer-Verlag Berlin Heidelberg

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Ziv, Y. et al. (1993). Complementation of the Cellular A-T Phenotype by Gene Transfer. In: Gatti, R.A., Painter, R.B. (eds) Ataxia-Telangiectasia. NATO ASI Series, vol 77. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78278-7_6

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  • DOI: https://doi.org/10.1007/978-3-642-78278-7_6

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-78280-0

  • Online ISBN: 978-3-642-78278-7

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