Hebert E, Diancourt F, Saint-Ruf G, Leng M
Centre de Biophysique Moléculaire, CNRS, Orleans, France.
Carcinogenesis. 1988 Jan;9(1):183-5. doi: 10.1093/carcin/9.1.183.
The mutation frequency and mutation spectrum resulting from 3-N-acetylamino-4,6-dimethyldipyrido[1,2-a:3',2'-d]imidazole (AGluP3) DNA adducts using a previously developed forward mutation assay were established. AGluP3-induced mutagenesis requires the umuC gene product(s) and exhibits similar amounts of base pair substitution and frameshift mutation. Comparison between these results and those obtained with the isosteric amine 2-N-acetylaminofluorene suggests the involvement of deacetylated adduct in the molecular mechanisms of AGluP3-induced mutagenesis.
利用先前开发的正向突变试验,确定了3-N-乙酰氨基-4,6-二甲基二吡啶并[1,2-a:3',2'-d]咪唑(AGluP3)DNA加合物产生的突变频率和突变谱。AGluP3诱导的诱变需要umuC基因产物,并且表现出相似数量的碱基对替换和移码突变。将这些结果与用等排胺2-N-乙酰氨基芴获得的结果进行比较,表明去乙酰化加合物参与了AGluP3诱导诱变的分子机制。