4.3 Article

Interplay between DNA polymerases β and λ in repair of oxidation DNA damage in chicken DT40 cells

期刊

DNA REPAIR
卷 6, 期 6, 页码 869-875

出版社

ELSEVIER
DOI: 10.1016/j.dnarep.2007.01.011

关键词

DNA polymerase lambda; DNA polymerase beta; oxidation DNA damage; DT40

资金

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [P30 CA016086-259035, P30-CA16086, P30 CA016086, P30 CA016086-24] Funding Source: Medline
  3. NIEHS NIH HHS [P42 ES005948, ES11746, R42 ES011746-05, P30 ES010126-07, P42 ES005948-070001, P42-ES05948, P30-ES10126, P30 ES010126, R42 ES011746-05S1, P42 ES005948-15, R42 ES011746] Funding Source: Medline

向作者/读者索取更多资源

DNA polymerase lambda (Pol lambda) is a DNA polymerase beta (Pol beta)-like enzyme with both DNA synthetic and 5'-deoxyribose-5'-phosphate lyase domains. Recent biochemical studies implicated Pol X as a backup enzyme to Pol beta in the mammalian base excision repair (BER) pathway. To examine the interrelationship between Pol lambda and Pol beta in BER of DNA damage in living cells, we disrupted the genes for both enzymes either singly or in combination in the chicken DT40 cell line and then characterized BER phenotypes. Disruption of the genes for both polymerases caused hypersensitivity to H2O2-induced cytotoxicity, whereas the effect of disruption of either polymerase alone was only modest. Similarly, BER capacity in cells after H2O2 exposure was lower in Pol beta(-/-) /Pol lambda(-/-) cells than in Pol beta(-/-), wild-type, and Pol lambda(-/-) cells, which were equivalent. These results suggest that these polymerases can complement for one another in counteracting oxidative DNA damage. Similar results were obtained in assays for in vitro BER capacity using cell extracts. With MMS-induced cytotoxicity, there was no significant effect on either survival or BER capacity from Pol X gene disruption. A strong hypersensitivity and reduction in BER capacity was observed for Pol beta(-/-)/Pol lambda(-/-) and Pol beta(-/-) cells, suggesting that Pol beta had a dominant role in counteracting alkylation DNA damage in this cell system. (c) 2007 Elsevier B.V. All rights reserved.

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