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Deficiency in DNA polymerase beta provokes replication-dependent apoptosis via DNA breakage, Bcl-2 decline and
Kirsten Ochs1, Jochen Lips, Simone Profittlich
1Division of Applied Toxicology, Institute of Toxicology, University of Mainz, Obere Zahlbacher Str. 67, D-55131 Mainz, Germany.
Abstract:
Cells deficient in DNA polymerase beta (beta-pol) are impaired in base excision repair (BER) and hypersensitive to various DNA damaging agents, including methylating mutagens. Hypersensitivity of beta-pol-deficient cells to methylating agents is because of induction of apoptosis (Ochs et al., Cancer Res., 59: 1544-1551, 1999), indicating incompletely repaired DNA damage to trigger the response. Here we show that defective BER in beta-pol-null cells results in an early and transient increase in the frequency of DNA single-strand breaks on treatment with methyl methanesulfonate. These breaks arising as repair intermediates are not likely to trigger apoptosis directly because they were repaired efficiently and generated both in resting and proliferating cells, whereas only proliferating cells underwent with high frequency apoptosis after methylation. Therefore, we propose that single-strand breaks are converted into another kind of critical apoptosis-triggering lesion during replication. These critical secondary DNA lesions are likely to be non-repaired DNA double-strand breaks (DSBs), which are formed at higher frequency in beta-pol-null than in wild-type cells. Apoptosis was a late response not detectable before 24 h after methylation and was preceded by DSBs formation, extensive chromosomal breakage, and decline in Bcl-2 level and caspase-9 and caspase-3 activation. Caspase-8 was not significantly activated. Transfection of beta-pol-null cells with bcl-2 protected against methylation-induced apoptosis, indicating Bcl-2 to be causally involved. Overall, the data demonstrate that in cells lacking beta-pol, defective BER results in incompletely repaired DNA damage, which triggers apoptosis in a replication-dependent way by activating the mitochondrial death pathway. It is suggested that DSBs act as a critical ultimate apoptosis-inducing lesion.
Insights
Cells lacking DNA polymerase beta (beta-pol) show defective DNA repair, leading to replication-dependent apoptosis. DNA double-strand breaks (DSBs) are identified as the critical lesion triggering this cell death pathway.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- DNA polymerase beta (beta-pol) is crucial for base excision repair (BER).
- Beta-pol-deficient cells exhibit hypersensitivity to methylating agents due to apoptosis.
- Incompletely repaired DNA damage is implicated in the hypersensitivity response.
Purpose of the Study:
- To investigate the mechanism underlying apoptosis in beta-pol-deficient cells treated with methylating agents.
- To identify the specific DNA lesions that trigger apoptosis in the absence of beta-pol.
- To elucidate the role of DNA double-strand breaks (DSBs) and the mitochondrial death pathway in this process.
Main Methods:
- Treatment of beta-pol-null and wild-type cells with methyl methanesulfonate.
- Analysis of DNA single-strand breaks and double-strand breaks (DSBs).
- Assessment of apoptosis, cell proliferation, Bcl-2 levels, and caspase activation.
- Complementation of beta-pol-null cells with beta-pol or Bcl-2.
Main Results:
- Defective BER in beta-pol-null cells leads to transient DNA single-strand breaks and increased DSBs during replication.
- Apoptosis is replication-dependent, occurring late after methylation and preceded by DSBs and chromosomal breakage.
- Bcl-2 expression protects against methylation-induced apoptosis, implicating the mitochondrial pathway.
Conclusions:
- In beta-pol-deficient cells, incomplete DNA repair during replication generates DSBs, which act as critical lesions inducing apoptosis.
- The mitochondrial death pathway, involving Bcl-2 and downstream caspases, mediates apoptosis in response to these DSBs.
- DSBs are the ultimate apoptosis-inducing lesions in this context, highlighting the importance of BER in preventing DNA damage-induced cell death.