Ataxia-telangiectasia: a multifaceted genetic disorder associated with defective signal transduction

Curr Opin Immunol. 1996 Aug;8(4):459-64. doi: 10.1016/s0952-7915(96)80030-6.

Abstract

The gene responsible for the defect in the human genetic disorder ataxia-telangiectasia, ATM, was cloned recently. The part of the gene coding for a phosphatidylinositol 3-kinase domain showed it to be related to a family of genes involved in signal transduction, cell cycle control and the response to DNA damage. The elucidation of the role of the ATM gene product will provide valuable insight into the radiosensitivity, cancer predisposition, immunodeficiency and neuropathology that characterize this syndrome.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Ataxia Telangiectasia / genetics*
  • Ataxia Telangiectasia / radiotherapy
  • Ataxia Telangiectasia Mutated Proteins
  • Cell Cycle Proteins
  • Cloning, Molecular
  • DNA-Binding Proteins
  • Humans
  • Leucine Zippers / genetics
  • Polymorphism, Genetic / genetics*
  • Protein Serine-Threonine Kinases*
  • Proteins / genetics
  • Radiation Tolerance / physiology
  • Signal Transduction / genetics*
  • Tumor Suppressor Proteins

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Proteins
  • Tumor Suppressor Proteins
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • Protein Serine-Threonine Kinases