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Open Access Research article

Comparison of clastogen-induced gene expression profiles in wild-type and DNA repair-deficient Rad54/Rad54B cells

Anuska G Mahabir13, Mirjam M Schaap1, Jeroen LA Pennings1*, Jan van Benthem1, Coenraad FM Hendriksen23 and Harry van Steeg1

Author Affiliations

1 National Institute for Public Health and the Environment (RIVM), Laboratory for Health Protection Research (GBO), P.O.Box 1, NL-3720 BA Bilthoven, the Netherlands

2 Netherlands Vaccine Institute (NVI), P.O.Box 457, NL-3720 AL Bilthoven, the Netherlands

3 Netherlands Centre Alternatives to Animal Use (NCA), P.O. Box 80.166, NL-3508 TD Utrecht, the Netherlands

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BMC Genomics 2010, 11:24  doi:10.1186/1471-2164-11-24

Published: 12 January 2010

Abstract

Background

Previously we found that Rad54/Rad54B cells are more sensitive towards mitomycin C (MMC) as compared to wild-type (WT) cells. This difference in sensitivity was absent upon exposure to other clastogens like bleomycin (BLM) and γ-radiation. In order to get further insight into possible underlying mechanisms, gene expression changes in WT and Rad54/Rad54B MEFs (mouse embryonic fibroblasts) after exposure to the clastogens MMC and BLM were investigated. Exposures of these cells to mutagens (N-ac-AAF and ENU) and vehicle were taken as controls.

Results

Most exposures resulted in an induction of DNA damage signaling and apoptosis genes and a reduced expression of cell division genes in cells of both genotypes. As expected, responses to N-ac-AAF were very similar in both genotypes. ENU exposure did not lead to significant gene expression changes in cells of both genotypes, presumably due to its short half-life. Gene expression responses to clastogens, however, showed a genotype-dependent effect for BLM and MMC. MMC treated Rad54/Rad54B MEFs showed no induction of p53-signaling, DNA damage response and apoptosis as seen for all the other treatments.

Conclusion

These data support our finding that different types of clastogens exist and that responses to these types depend on the DNA repair status of the cells.