Glickman B W, Schaaper R M, Haseltine W A, Dunn R L, Brash D E
Proc Natl Acad Sci U S A. 1986 Sep;83(18):6945-9. doi: 10.1073/pnas.83.18.6945.
Mutation induced by ultraviolet light is predominantly targeted by UV photoproducts. Two primary candidates for the premutagenic lesion are the cyclobutane pyrimidine dimer and the less frequent (by a factor of 10) pyrimidine-pyrimidone (6-4) photoproduct. Methylation of the 3'-cytosine in the sequence 5' CCAGG 3' reduces the yield of (6-4) lesions, but not of cyclobutane dimers, at these sites. By taking advantage of mutants deficient in cytosine methylation, we show here that at the three sites in the lacI gene of Escherichia coli having this sequence, the specific increase in the formation of the (6-4) photoproducts is accompanied by a concomitant increase in mutation. At each site, a G X C to A X T transition results in an amber mutation. In the unmethylated state, these sites become among the most frequent nonsense mutations recovered. We conclude that the (6-4) photoproduct constitutes a major premutagenic lesion in E. coli.
紫外线诱导的突变主要针对紫外线光产物。诱变前体损伤的两个主要候选物是环丁烷嘧啶二聚体和频率较低(相差10倍)的嘧啶 - 嘧啶酮(6-4)光产物。在序列5' CCAGG 3'中3'-胞嘧啶的甲基化降低了这些位点处(6-4)损伤的产生率,但不影响环丁烷二聚体的产生率。通过利用胞嘧啶甲基化缺陷的突变体,我们在此表明,在大肠杆菌lacI基因中具有该序列的三个位点处,(6-4)光产物形成的特异性增加伴随着突变的相应增加。在每个位点,G X C到A X T的转变导致琥珀突变。在未甲基化状态下,这些位点成为恢复的最常见无义突变之一。我们得出结论,(6-4)光产物是大肠杆菌中的主要诱变前体损伤。