Sharma R C, Smith K C
Mutat Res. 1986 Jul;166(1):23-8. doi: 10.1016/0167-8817(86)90037-4.
Ultraviolet (UV)-irradiated uvrB recF and uvrB recB cells of Escherichia coli K-12 showed similar radiation sensitivities when plated on minimal growth medium (MM), however, the uvrB recF cells were much more UV radiation-sensitive than the uvrB recB cells when plated on rich growth medium. Sedimentation analysis of the DNA from UV-irradiated uvrB recF cells suggests that the rich medium killing of uvrB recF cells is due to the inhibition of the repair of UV-radiation-induced DNA double-strand breaks, i.e., the killing is due to the inhibition of the recB-dependent pathway of postreplication repair. Furthermore, we demonstrated that the DNA double-strand breaks that were formed in UV-irradiated uvrB recA200(Ts) cells incubated at 42 degrees C in rich growth medium were not repaired whether the medium during subsequent repair incubation at 30 degrees C was MM or rich growth medium, while DNA double-strand breaks that were formed in MM at 42 degrees C could be repaired in MM or in rich growth medium at 30 degrees C. How the absence of an abrupt slowing of DNA synthesis when UV-irradiated cells are held in rich growth medium (Sharma and Smith, 1985b) may prevent the repair of these DNA double-strand breaks is discussed.
将大肠杆菌K-12的紫外线(UV)照射过的uvrB recF和uvrB recB细胞接种在基本生长培养基(MM)上时,它们表现出相似的辐射敏感性,然而,当接种在丰富生长培养基上时,uvrB recF细胞比uvrB recB细胞对紫外线辐射更敏感。对紫外线照射过的uvrB recF细胞的DNA进行沉降分析表明,丰富培养基中uvrB recF细胞的死亡是由于紫外线辐射诱导的DNA双链断裂修复受到抑制,即细胞死亡是由于复制后修复的recB依赖性途径受到抑制。此外,我们证明,在丰富生长培养基中于42℃孵育的紫外线照射过的uvrB recA200(Ts)细胞中形成的DNA双链断裂,无论在随后30℃修复孵育期间的培养基是MM还是丰富生长培养基,都不会被修复,而在42℃于MM中形成的DNA双链断裂在30℃时可在MM或丰富生长培养基中被修复。本文讨论了当紫外线照射过的细胞置于丰富生长培养基中时(Sharma和Smith,1985b)DNA合成没有突然减慢是如何阻止这些DNA双链断裂的修复的。