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大肠杆菌中由X射线和过氧化氢引起的氧化性DNA损伤的多种修复途径。

Multiple pathways for repair of oxidative DNA damages caused by X rays and hydrogen peroxide in Escherichia coli.

作者信息

Zhang Q M, Yonei S, Kato M

机构信息

Laboratory of Radiation Biology, Faculty of Science, Kyoto University, Japan.

出版信息

Radiat Res. 1992 Dec;132(3):334-8.

PMID:1282265
Abstract

The responses of Escherichia coli to X rays and hydrogen peroxide were examined in mutants which are deficient in one or more DNA repair genes. Mutant cells deficient in either exonuclease III (xthA) or endonuclease IV (nfo) had normal resistance to X rays, but an xthA-nfo double mutant showed a sensitivity increased over that of either parental strain. A DNA polymerase I mutant (polA) was more sensitive than the xthA-nfo mutant. Cells bearing mutations in all of the polA, xthA, and nfo genes were more sensitive to X rays than polA and xthA-nfo mutants. Similar repair responses were obtained by exposing these mutant cells to hydrogen peroxide, with the exception of the xthA mutant, which was hypersensitive to this agent. The DNA polymerase III mutant (polC(Ts)) was slightly more sensitive to the agents than the wild-type strain at the restrictive temperature. The sensitivity of the polC-xthA-nfo mutant to X rays and hydrogen peroxide was greater than that of polC but almost the same as that of the xthA-nfo mutant. From these results it appears that there are at least four repair pathways, the DNA polymerase I-, exonuclease III/endonuclease IV and DNA polymerase I-, exonuclease III/endonuclease IV and DNA polymerase III-, and exonuclease III/endonuclease IV-dependent pathways, for the repair of oxidative DNA damages in E. coli.

摘要

在一个或多个DNA修复基因存在缺陷的突变体中,研究了大肠杆菌对X射线和过氧化氢的反应。缺乏核酸外切酶III(xthA)或核酸内切酶IV(nfo)的突变细胞对X射线具有正常抗性,但xthA-nfo双突变体显示出比任一亲本菌株更高的敏感性。DNA聚合酶I突变体(polA)比xthA-nfo突变体更敏感。在polA、xthA和nfo基因均发生突变的细胞对X射线的敏感性高于polA和xthA-nfo突变体。将这些突变细胞暴露于过氧化氢时,除了对该试剂超敏感的xthA突变体外,获得了类似的修复反应。DNA聚合酶III突变体(polC(Ts))在限制温度下对这些试剂的敏感性略高于野生型菌株。polC-xthA-nfo突变体对X射线和过氧化氢的敏感性高于polC,但几乎与xthA-nfo突变体相同。从这些结果看来,大肠杆菌中至少存在四种修复途径,即DNA聚合酶I-、核酸外切酶III/核酸内切酶IV依赖途径,DNA聚合酶I-、核酸外切酶III/核酸内切酶IV和DNA聚合酶III-依赖途径,以及核酸外切酶III/核酸内切酶IV依赖途径,用于修复氧化性DNA损伤。

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