Gutman P D, Fuchs P, Minton K W
Department of Pathology, F. E. Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814-4799.
Mutat Res. 1994 Jan;314(1):87-97. doi: 10.1016/0921-8777(94)90064-7.
Deinococcus radiodurans and other species of this genus share extreme resistance to ionizing radiation and many other agents that damage DNA. D. radiodurans mutant strains defective in a deinococcal DNA polymerase that is homologous with E. coli DNA polymerase I are highly sensitive to DNA damage. In the current work we have inquired whether E. coli DNA Pol I can substitute for D. radiodurans Pol in partially or fully restoring to pol- D. radiodurans mutants the extreme DNA damage-resistance typical of this organism. The E. coli polA gene or a 5'-truncated polA gene that encodes the Klenow fragment were introduced and expressed in two different D. radiodurans pol- mutants: Strain 303, which is a chemically mutagenized derivative, and strain 6R1A, which is isogenic with wild-type D. radiodurans except for an insertional mutation within the pol gene. Expression of E. coli polA in both of these mutants fully restored wild-type resistance to ionizing- and UV254-radiation and mitomycin-C exposure. Expression of the Klenow fragment-encoding gene restored wild-type resistance to D. radiodurans strain 303, but only partial resistance to strain 6R1A. The observation that E. coli DNA Pol I is as effective as D. radiodurans Pol in restoring damage resistance, indicates that D. radiodurans DNA Pol per se does not have special properties that are essential or prerequisite for expression of the extreme resistance of D. radiodurans.
耐辐射球菌及该属的其他物种对电离辐射和许多其他能损伤DNA的因子具有极强的抗性。耐辐射球菌中一种与大肠杆菌DNA聚合酶I同源的DNA聚合酶存在缺陷的突变菌株,对DNA损伤高度敏感。在当前的研究中,我们探究了大肠杆菌DNA聚合酶I是否能够部分或完全替代耐辐射球菌的DNA聚合酶,从而使耐辐射球菌pol-突变体恢复该生物体典型的对DNA损伤的极端抗性。将编码Klenow片段的大肠杆菌polA基因或5'-截短的polA基因导入两种不同的耐辐射球菌pol-突变体中并表达:菌株303,它是化学诱变的衍生物;以及菌株6R1A,除了pol基因内的插入突变外,它与野生型耐辐射球菌同基因。在这两种突变体中表达大肠杆菌polA均能完全恢复对电离辐射、UV254辐射和丝裂霉素C暴露的野生型抗性。表达编码Klenow片段的基因可使耐辐射球菌菌株303恢复野生型抗性,但仅能使菌株6R1A恢复部分抗性。大肠杆菌DNA聚合酶I在恢复损伤抗性方面与耐辐射球菌的DNA聚合酶一样有效,这一观察结果表明,耐辐射球菌的DNA聚合酶本身并不具有对于耐辐射球菌表达极端抗性至关重要或必不可少的特殊性质。