Sedgwick B
Imperial Cancer Research Fund, Clare Hall Laboratories, Herts, UK.
J Cell Sci Suppl. 1987;6:215-23. doi: 10.1242/jcs.1984.supplement_6.15.
Exposure of Escherichia coli to simple alkylating agents, such as methylnitrosourea, causes the induction of at least three DNA repair functions that are under the control of the ada gene. The ada gene product itself repairs several O-methylated lesions in DNA, including methylphosphotriesters and the mutagenic adduct O6-methylguanine. The methyl groups are transferred from these lesions on to two different cysteine residues within the Ada protein resulting in self-methylation. We have found that the Ada protein is converted to an activator of expression of genes involved in the adaptive response after accepting a methyl group from a methylphosphotriester, but not from O6-methylguanine. This was shown using the in vitro techniques of DNA-dependent protein synthesis and run-off transcription. Delayed electrophoretic migration and footprinting experiments have shown that the methylated activator of transcription binds to specific DNA sequences immediately upstream from the RNA polymerase binding sites in the promoter regions of the inducible genes. The Ada protein-binding sites contain the common sequence d(A-A-A-N-N-A-A-A-G-C-G-C-A).
大肠杆菌暴露于简单的烷基化剂,如甲基亚硝基脲,会诱导至少三种受ada基因控制的DNA修复功能。ada基因产物本身可修复DNA中的几种O-甲基化损伤,包括甲基磷酸三酯和诱变加合物O6-甲基鸟嘌呤。甲基从这些损伤部位转移到Ada蛋白内的两个不同半胱氨酸残基上,导致自身甲基化。我们发现,Ada蛋白从甲基磷酸三酯而非O6-甲基鸟嘌呤接受甲基后,会转变为参与适应性反应的基因表达激活剂。这是通过依赖DNA的蛋白质合成和连续转录的体外技术证明的。延迟电泳迁移和足迹实验表明,甲基化的转录激活剂与诱导型基因启动子区域中RNA聚合酶结合位点上游紧邻的特定DNA序列结合。Ada蛋白结合位点包含共同序列d(A-A-A-N-N-A-A-A-G-C-G-C-A)。