Mutagenesis, Vol. 16, No. 5, 419-422,
September 2001
© 2001 UK Environmental Mutagen Society/Oxford University Press
Ataxia telangiectasia: G2 checkpoint and chromosomal damage in proliferating lymphocytes
1 Programa de Genética Humana and Departamento de Pediatría y Cirugía Infantil, Facultad de Medicina, Universidad de Chile, Santiago, Chile, 2 Centro de Investigaciones Biológicas, CSIC, Velázquez, 144 Madrid-28006, Spain and 3 Departamento de Biología, Universidad Autónoma de Madrid, Canto Blanco, Madrid, Spain
There is a checkpoint pathway in eukaryotic cells that depends on ATM (ataxia telangiectasia mutated) kinase which activates the processes leading to the repair of DNA damage and also lengthens the G2 stage of the cell cycle. In cells from ataxia telangiectasia patients, due to their lack of active ATM kinase, an increase in chromosomal aberrations and a failure to induce G2 lengthening could be expected. However, the basal G2 timing in ataxia telangiectasia cells was longer than in controls and was further extended after X-ray irradiation (0.4 Gy), although to a lesser extent than in controls. Moreover, in control cells caffeine shortened G2 and increased chromosomal damage 7-fold, while in ataxia telangiectasia cells caffeine only trebled aberration yield without shortening G2. As caffeine is an inhibitor of ATM kinase, these results suggest the existence of some redundant ATM-independent checkpoint in G2 of ataxia telangiectasia cells. The differential response to caffeine of ataxia telangiectasia and control lymphocytes may be explained by the presence of two different subpathways in the G2 checkpoint: one regulating the processing and repair of damaged DNA and the other controlling G2 timing. While in controls both subpathways may be mediated by ATM kinase, in ataxia telangiectasia cells caffeine-sensitive ATR kinase and the caffeine-insensitive DNA-PK kinases might be responsible for DNA repair and the G2 delay subpathways, respectively. Confirmation of this model in ataxia telangiectasia cells with another cell type in which both subpathways are mediated by DNA-PK should define whether a metylxanthine such as caffeine may also have an additional direct inhibitory effect on DNA repair.
4 To whom correspondence should be addressed. Tel: +34 91 564 45 62; Fax: + 34 91 562 75 18; Email: delatorrec{at}cib.csic.es
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