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DNA的3'端阻断损伤作为过氧化氢在大肠杆菌中引起的致突变性损伤。

3'-blocking damage of DNA as a mutagenic lesion caused by hydrogen peroxide in Escherichia coli.

作者信息

Takemoto T, Zhang Q M, Matsumoto Y, Mito S, Izumi T, Ikehata H, Yonei S

机构信息

Laboratory of Radiation Biology, Graduate School of Science, Kyoto University, Japan.

出版信息

J Radiat Res. 1998 Jun;39(2):137-44. doi: 10.1269/jrr.39.137.

Abstract

Ionizing radiation and hydrogen peroxide (H2O2) produce many types of oxidative DNA damage such as strand breaks, apurinic/apyrimidinic (AP) sites, base modifications and 3'-blocking damage such as 3'-phosphoglycolated and 3'-phosphorylated termini. AP sites and 3'-blocking damage are repairable by exonuclease III and endonuclease IV in Escherichia coli. XthA-nfo double mutants of E. coli, which are deficient in exonuclease III and endonuclease IV, were highly sensitive to lethal and mutagenic effects of H2O2, compared with the wild-type strains. The pNT180 and pNT186 plasmids containing wild-type nfo and mutant nfo-186 gene, respectively, were introduced into the xthA-nfo mutant. The nfo-186 gene product, Nfo186, retained normal AP endonuclease activity but could not remove 3'-blocking damage from DNA. The pNT180 corrected the sensitivity of the xthA-nfo mutant to lethal and mutagenic effects of H2O2. On the other hand, the pNT186 did not have any complementation effects. From these results it was concluded that 3'-blocking damage rather than an AP site is the primary lesion responsible for both lethal and mutagenic effects of H2O2.

摘要

电离辐射和过氧化氢(H2O2)会产生多种类型的氧化性DNA损伤,如链断裂、脱嘌呤/脱嘧啶(AP)位点、碱基修饰以及3'端阻断损伤,如3'-磷酸乙醇酸化和3'-磷酸化末端。在大肠杆菌中,AP位点和3'端阻断损伤可由外切核酸酶III和内切核酸酶IV修复。与野生型菌株相比,缺乏外切核酸酶III和内切核酸酶IV的大肠杆菌XthA-nfo双突变体对H2O2的致死和诱变作用高度敏感。分别将含有野生型nfo和突变型nfo-186基因的pNT180和pNT186质粒导入xthA-nfo突变体中。nfo-186基因产物Nfo186保留了正常的AP内切核酸酶活性,但无法从DNA中去除3'端阻断损伤。pNT180纠正了xthA-nfo突变体对H2O2致死和诱变作用的敏感性。另一方面,pNT186没有任何互补作用。从这些结果可以得出结论,H2O2的致死和诱变作用的主要损伤是3'端阻断损伤而非AP位点。

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