Tano Keizo, Nakamura Jun, Asagoshi Kenjiro, Arakawa Hiroshi, Sonoda Eiichiro, Braithwaite Elena K, Prasad Rajendra, Buerstedde Jean-Marie, Takeda Shunichi, Watanabe Masami, Wilson Samuel H
Research Reactor Institute, Kyoto University, Kumatori, Japan.
DNA Repair (Amst). 2007 Jun 1;6(6):869-75. doi: 10.1016/j.dnarep.2007.01.011. Epub 2007 Mar 23.
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 lambda 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 H(2)O(2)-induced cytotoxicity, whereas the effect of disruption of either polymerase alone was only modest. Similarly, BER capacity in cells after H(2)O(2) 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 lambda 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.
DNA聚合酶λ(Pol λ)是一种类似DNA聚合酶β(Pol β)的酶,具有DNA合成和5'-脱氧核糖-5'-磷酸裂解酶结构域。最近的生化研究表明,在哺乳动物碱基切除修复(BER)途径中,Pol λ作为Pol β的备用酶。为了研究活细胞中DNA损伤的BER过程中Pol λ和Pol β之间的相互关系,我们在鸡DT40细胞系中单独或联合破坏这两种酶的基因,然后对BER表型进行了表征。两种聚合酶基因的破坏导致对H₂O₂诱导的细胞毒性超敏,而单独破坏任何一种聚合酶的影响都较小。同样,H₂O₂暴露后细胞中的BER能力在Pol β(-/-)/Pol λ(-/-)细胞中低于Pol β(-/-)、野生型和Pol λ(-/-)细胞,而后三者相当。这些结果表明,这些聚合酶在对抗氧化性DNA损伤方面可以相互补充。使用细胞提取物进行体外BER能力测定也得到了类似结果。对于甲基磺酸甲酯(MMS)诱导的细胞毒性,Pol λ基因破坏对细胞存活或BER能力均无显著影响。在Pol β(-/-)/Pol λ(-/-)和Pol β(-/-)细胞中观察到强烈的超敏反应和BER能力降低,表明在该细胞系统中,Pol β在对抗烷基化DNA损伤方面起主导作用。