| First Author | Lavin MF | Year | 1999 |
| Journal | Int J Biochem Cell Biol | Volume | 31 |
| Issue | 7 | Pages | 735-40 |
| PubMed ID | 10467728 | Mgi Jnum | J:59507 |
| Mgi Id | MGI:1351742 | Doi | 10.1016/s1357-2725(99)00028-x |
| Citation | Lavin MF (1999) ATM: the product of the gene mutated in ataxia-telangiectasia. Int J Biochem Cell Biol 31(7):735-40 |
| abstractText | Ataxia-telangiectasia mutated (ATM) is the product of the gene mutated in the human genetic disorder ataxia-telangeictasia (A-T). It is a 370 kDa protein that is a member of the phosphatidyl inositol 3-kinases superfamily. A-T cells and those derived from Atm-/- mice are characterized by hypersensitivity to ionizing radiation and defective cell cycle checkpoints. Defects are observed at all cell cycle checkpoints in A-T cells post-irradiation including the G1/S interface where ATM plays an important role in the activation of the tumour suppressor gene product p53. Activation leads to the induction of p21/WAF1, inhibition of cyclin-dependent kinase activity, failure to phosphorylate key substrates such as the retinoblastoma protein and consequently G1 arrest. ATM also plays an important role in the regulation and surveillance of meiotic progression. Absence of ATM gives rise to a spectrum of defects including immunodeficiency, neurodegeneration, radiosensitivity and cancer predisposition. It is clear that a better definition of the role of ATM in DNA damage recognition, cell cycle control and cell signalling may assist in the treatment of the progressive neurodegeneration in this syndrome. |
