Conkling M A, Drake J W
Genetics. 1984 Aug;107(4):525-36. doi: 10.1093/genetics/107.4.525.
When ultraviolet-irradiated bacteriophage T4 is assayed at plating temperatures ranging from 20 degrees to 40 degrees, its survival increases at the higher temperatures. This "thermal rescue" requires an intact WXY system but not the denV pyrimidine dimer excision system. Mutation rates decrease with increasing temperature, indicating that some lesions processed in a mutagenic manner at lower temperatures are accurately repaired or circumvented at high temperatures. When both the cold sensitivity of UV survival in the wild type and the temperature sensitivity of newly isolated ts mutants of uvsX and uvsY were used, expression of the WXY system was monitored in temperature shift UV survival experiments and was found to be biphasic: the uvsX and uvsY functions increase UV survival in two increments, one at an early and another at a late stage of infection. The uvsW function, however, increases UV survival only early in infection.
当在20摄氏度至40摄氏度的铺板温度下检测经紫外线照射的噬菌体T4时,其存活率在较高温度下会增加。这种“热拯救”需要完整的WXY系统,但不需要denV嘧啶二聚体切除系统。突变率随温度升高而降低,这表明一些在较低温度下以诱变方式处理的损伤在高温下能被准确修复或规避。当同时利用野生型紫外线存活率的冷敏感性以及新分离的uvsX和uvsY温度敏感型ts突变体的温度敏感性时,在温度转换紫外线存活率实验中监测WXY系统的表达,发现其具有双相性:uvsX和uvsY功能以两种增量增加紫外线存活率,一种在感染早期,另一种在感染后期。然而,uvsW功能仅在感染早期增加紫外线存活率。