Cloning and Expression of Large Mammalian cDNAs: Lessons from ATM

  • Yosef Shiloh
  • Anat Bar-Shira
  • Yaron Galanty
  • Yael Ziv
Part of the Genetic Engineering book series (GEPM, volume 20)


The ATM gene and its protein product have recently become a focus of interest for clinicians, biologists and cancer epidemiologists. The ATM protein is involved in a complex junction of signal transduction pathways linking cellular stress responses, cell cycle control and specific developmental processes (1). The ATM gene was identified by virtue of its responsibility for a human genetic disorder, ataxia- telangiectasia (A-T). A-T is an autosomal recessive disease characterized by cerebellar degeneration, immunodeficiency, premature aging, cancer predisposition and radiation sensitivity. A-T cells exhibit chromosomal instability, extreme sensitivity to ionizing radiation and radiomimetic chemicals, defective cell cycle checkpoints, and defects in several signal transduction pathways that respond to mitogenic stimuli and genotoxic stress (see refs. 1, 2 for recent reviews).


Autosomal Recessive Disease Flag Epitope Episomal Vector Huntington Disease Gene Metal Chelate Chromatography 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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Copyright information

© Springer Science+Business Media New York 1998

Authors and Affiliations

  • Yosef Shiloh
    • 1
  • Anat Bar-Shira
    • 1
  • Yaron Galanty
    • 1
  • Yael Ziv
    • 1
  1. 1.Department of Human Genetics, Sackler School of MedicineTel Aviv UniversityRamat AvivIsrael

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