Activation of the Cellular DNA Damage Response in the Absence of DNA Lesions
Top Cited Papers
- 13 June 2008
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 320 (5882), 1507-1510
- https://doi.org/10.1126/science.1159051
Abstract
The cellular DNA damage response (DDR) is initiated by the rapid recruitment of repair factors to the site of DNA damage to form a multiprotein repair complex. How the repair complex senses damaged DNA and then activates the DDR is not well understood. We show that prolonged binding of DNA repair factors to chromatin can elicit the DDR in an ATM (ataxia telangiectasia mutated)– and DNAPK (DNA-dependent protein kinase)–dependent manner in the absence of DNA damage. Targeting of single repair factors to chromatin revealed a hierarchy of protein interactions within the repair complex and suggests amplification of the damage signal. We conclude that activation of the DDR does not require DNA damage and stable association of repair factors with chromatin is likely a critical step in triggering, amplifying, and maintaining the DDR signal.Keywords
This publication has 21 references indexed in Scilit:
- Spatial organization of the mammalian genome surveillance machinery in response to DNA strand breaksThe Journal of cell biology, 2006
- γH2AX and MDC1: Anchoring the DNA-damage-response machinery to broken chromosomesDNA Repair, 2006
- MDC1 Maintains Genomic Stability by Participating in the Amplification of ATM-Dependent DNA Damage SignalsMolecular Cell, 2006
- MDC1 Directly Binds Phosphorylated Histone H2AX to Regulate Cellular Responses to DNA Double-Strand BreaksCell, 2005
- Dynamic assembly and sustained retention of 53BP1 at the sites of DNA damage are controlled by Mdc1/NFBD1The Journal of cell biology, 2005
- Identification and Characterization of a Novel and Specific Inhibitor of the Ataxia-Telangiectasia Mutated Kinase ATMCancer Research, 2004
- Watching the DNA Repair Ensemble DanceCell, 2004
- Mdc1 couples DNA double-strand break recognition by Nbs1 with its H2AX-dependent chromatin retentionThe EMBO Journal, 2004
- Chk1 and Chk2 kinases in checkpoint control and cancerCancer Cell, 2003
- ATM: Ready, Set, GoCell Cycle, 2003