Rapid activation of ATM on DNA flanking double-strand breaks

You, Zhongsheng, Bailis, Julie M., Johnson, Sam A., Dilworth, Stephen M. ORCID: https://orcid.org/0000-0001-9815-0004 and Hunter, Tony (2007) Rapid activation of ATM on DNA flanking double-strand breaks. Nature Cell Biology, 9 (11) . pp. 1311-1318. ISSN 1465-7392 [Article] (doi:10.1038/ncb1651)


The tumour-suppressor gene ATM, mutations in which cause the human genetic disease ataxia telangiectasia (A-T), encodes a key protein kinase that controls the cellular response to DNA double-strand breaks (DSBs). DNA DSBs caused by ionizing radiation or chemicals result in rapid ATM autophosphorylation, leading to checkpoint activation and phosphorylation of substrates that regulate cell-cycle progression, DNA repair, transcription and cell death. However, the precise mechanism by which damaged DNA induces ATM and checkpoint activation remains unclear. Here, we demonstrate that linear DNA fragments added to Xenopus egg extracts mimic DSBs in genomic DNA and provide a platform for ATM autophosphorylation and activation. ATM autophosphorylation and phosphorylation of its substrate NBS1 are dependent on DNA fragment length and the concentration of DNA ends. The minimal DNA length required for efficient ATM autophosphorylation is approximately 200 base pairs, with cooperative autophosphorylation induced by DNA fragments of at least 400 base pairs. Importantly, full ATM activation requires it to bind to DNA regions flanking DSB ends. These findings reveal a direct role for DNA flanking DSB ends in ATM activation.

Item Type: Article
Research Areas: A. > School of Science and Technology > Natural Sciences > Molecular Biology group
A. > School of Science and Technology > Natural Sciences
Item ID: 10101
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Depositing User: Professor Stephen M. Dilworth
Date Deposited: 19 Feb 2013 06:37
Last Modified: 13 Oct 2016 14:26
URI: https://eprints.mdx.ac.uk/id/eprint/10101

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