Zhestianikov V D, Savel'eva G E, Ziganshina E Kh
Institute of Cytology RAS, St. Petersburg.
Tsitologiia. 2002;44(5):499-501.
In UV-irradiated E. coli WP2 uvrA, deficient in excision repair of DNA with pyrimidine dimers, gamma-irradiation in low doses (radioadaptation) before UV-irradiation leads to the intensification of postreplication repair of DNA. This process in WP2 uvrA polA and uvrA lexA mutants is less than in WP2 uvrA cells, but in WP2 uvrA recA both postreplication repair and its radioadaptive intensification are absent. In E. coli AB1157 excising pyrimidine dimers the radioadaptive intensification of postreplication repair of DNA is expressed almost to the same extent as in WP2 uvrA. In GW2100 umuC mutant, deficient in DNA polymerase V, postreplication repair of DNA is expressed, but its radioadaptive intensification is absent, while in AB2463 recA13 both postreplication repair of DNA and radioadaptive intensification of postreplication repair of DNA are absent. The above data suggest that DNA polymerase I and LexA protein are needed for radioadaptive intensification of postreplication repair of DNA in uvrA strain, and DNA polymerase V is needed for radioadaptive intensification in E. coli AB1157, and that RecA protein is required for postreplication repair and radioadaptive intensification of postreplication repair of DNA.
在紫外线照射的大肠杆菌WP2 uvrA中,其缺乏对含嘧啶二聚体的DNA进行切除修复的能力,在紫外线照射前进行低剂量γ射线照射(辐射适应)会导致DNA复制后修复增强。在WP2 uvrA polA和uvrA lexA突变体中的这一过程比在WP2 uvrA细胞中要弱,但在WP2 uvrA recA中,复制后修复及其辐射适应性增强均不存在。在能够切除嘧啶二聚体的大肠杆菌AB1157中,DNA复制后修复的辐射适应性增强程度与在WP2 uvrA中几乎相同。在缺乏DNA聚合酶V的GW2100 umuC突变体中,存在DNA复制后修复,但不存在其辐射适应性增强,而在AB2463 recA13中,DNA复制后修复以及DNA复制后修复的辐射适应性增强均不存在。上述数据表明,uvrA菌株中DNA复制后修复的辐射适应性增强需要DNA聚合酶I和LexA蛋白,大肠杆菌AB1157的辐射适应性增强需要DNA聚合酶V,并且RecA蛋白是DNA复制后修复及其辐射适应性增强所必需的。