Profiling DNA damage response following mitotic perturbations.
Ronni S PedersenGopal KaremoreThorkell GudjonssonMaj-Britt RaskBeate NeumannJean-Karim HérichéRainer PepperkokJan EllenbergDaniel Wolfram GerlichJiri LukasClaudia LukasPublished in: Nature communications (2016)
Genome integrity relies on precise coordination between DNA replication and chromosome segregation. Whereas replication stress attracted much attention, the consequences of mitotic perturbations for genome integrity are less understood. Here, we knockdown 47 validated mitotic regulators to show that a broad spectrum of mitotic errors correlates with increased DNA breakage in daughter cells. Unexpectedly, we find that only a subset of these correlations are functionally linked. We identify the genuine mitosis-born DNA damage events and sub-classify them according to penetrance of the observed phenotypes. To demonstrate the potential of this resource, we show that DNA breakage after cytokinesis failure is preceded by replication stress, which mounts during consecutive cell cycles and coincides with decreased proliferation. Together, our results provide a resource to gauge the magnitude and dynamics of DNA breakage associated with mitotic aberrations and suggest that replication stress might limit propagation of cells with abnormal karyotypes.
Keyphrases
- cell cycle
- induced apoptosis
- circulating tumor
- dna damage response
- dna damage
- cell free
- cell cycle arrest
- single molecule
- signaling pathway
- single cell
- oxidative stress
- dna repair
- endoplasmic reticulum stress
- stress induced
- emergency department
- nucleic acid
- stem cells
- cell death
- cell therapy
- working memory
- dna methylation
- mesenchymal stem cells
- risk assessment