Park S D, Choi K H, Hong S W, Cleaver J E
Mutat Res. 1981 Jul;82(2):365-71. doi: 10.1016/0027-5107(81)90165-2.
Unscheduled DNA synthesis and excision of pyrimidine dimers in human cells exposed to ultraviolet let were inhibited by exposure to methyl methanesulfonate (MMS, 1-2 mM), but repair of MMS damage was not inhibited by UV light. Because the pathways for excision of pyrimidine dimers and alkylation damage have previously been shown to be different, this observation implies a direct effect of alkylation on repair enzymes. We estimate that if inhibition is due to protein alkylation, the UV repair system must present an extremely large target to alkylation and may involve a complex of protein subunits in the order of 1 million daltons such that 1 or more alkylations occur per complex at the concentrations used. These results also indicate that the method of exposing cells to 2 DNA-damaging agents to determine whether they are repaired by common or different pathways can be quite unreliable because of other effects on the repair systems themselves.
暴露于紫外线的人类细胞中,嘧啶二聚体的非预定DNA合成及切除受到甲基磺酸甲酯(MMS,1 - 2 mM)的抑制,但紫外线对MMS损伤的修复并无抑制作用。由于此前已表明嘧啶二聚体切除途径与烷基化损伤途径不同,该观察结果暗示烷基化对修复酶有直接影响。我们估计,如果抑制是由于蛋白质烷基化导致的,那么紫外线修复系统必定是烷基化的一个极大靶点,且可能涉及一个约100万道尔顿的蛋白质亚基复合物,以至于在所用浓度下每个复合物会发生1次或更多次烷基化。这些结果还表明,通过将细胞暴露于两种DNA损伤剂来确定它们是通过共同途径还是不同途径进行修复的方法可能相当不可靠,因为这会对修复系统本身产生其他影响。