Crossref journal-article
Cold Spring Harbor Laboratory
Genes & Development (246)
Abstract

The gene mutated in ataxia-telangiectasia (AT) patients, denoted ATM, encodes a putative protein or lipid kinase. To elucidate the functions of ATM, we disrupted the mouse ATM gene through homologous recombination in mice. Consistent with cellular defects of AT patients, the ATM-/- cells are hypersensitive to gamma-irradiation and defective in cell-cycle arrest following radiation, correlating with a defective up-regulation of p53. In addition, ATM-/- mouse thymocytes are more resistant to apoptosis induced by gamma-irradiation than normal thymocytes. ATM-/- fibroblasts are inefficient in G1 to S-phase progression following serum stimulation and senesce after only a few passages in culture. They have an increased constitutive level of p21CP1/WAF1. The ATM protein is therefore critical both for cellular responses to ionizing radiation and for normal cell-cycle progression. ATM+/- fibroblasts and thymocytes showed intermediately defective responses to irradiation but no growth defect, suggesting that the increased cancer risk of AT heterozygotes could be attributable to poor checkpoint function.

Bibliography

Xu, Y., & Baltimore, D. (1996). Dual roles of ATM in the cellular response to radiation and in cell growth control. Genes & Development, 10(19), 2401–2410.

Authors 2
  1. Y Xu (first)
  2. D Baltimore (additional)
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Dates
Type When
Created 18 years, 2 months ago (June 5, 2007, 5:15 p.m.)
Deposited 3 years, 9 months ago (Nov. 14, 2021, 9:54 p.m.)
Indexed 1 month, 3 weeks ago (July 2, 2025, 2:33 p.m.)
Issued 28 years, 10 months ago (Oct. 1, 1996)
Published 28 years, 10 months ago (Oct. 1, 1996)
Published Online 28 years, 10 months ago (Oct. 1, 1996)
Published Print 28 years, 10 months ago (Oct. 1, 1996)
Funders 0

None

@article{Xu_1996, title={Dual roles of ATM in the cellular response to radiation and in cell growth control.}, volume={10}, ISSN={1549-5477}, url={http://dx.doi.org/10.1101/gad.10.19.2401}, DOI={10.1101/gad.10.19.2401}, number={19}, journal={Genes & Development}, publisher={Cold Spring Harbor Laboratory}, author={Xu, Y and Baltimore, D}, year={1996}, month=oct, pages={2401–2410} }