Meng Z, Hsie A W
Division of Environmental Biological Toxicology, Shanxi University, Taiyuan.
Yi Chuan Xue Bao. 1997 Oct;24(5):403-9.
In this study, we examined the mutagenicity of sodium arsenite at the xathine-guanine phosphoribosyl transferase locus (gpt) in a pSV2 gpt-transformed CHO cell line AS52. The chemical induced a dose-dependent increase of mutant frequency at the locus. Nested PCR analysis revealed that the majority of arsenite-induced AS52 mutants had totally deleted the gpt gene. For the spontaneous, 50 mumol/L arsenite--and 100 mumol/L arsenite--induced mutants in AS52 cells, the percentages of total deletion of the gpt gene were 36.00%, 54.72% and 66.67% respectively. The PCR products of gpt gene from nine 100 mumo/L sodium bisulfite-induced mutants were analyzed with direct DNA sequence technology. The frameshift mutation was identified in two mutants (2/9). No genomic alteration could be found in the structural gene examined in the other 7 mutants, where their molecular alterations probably located in the promoter region.
在本研究中,我们检测了亚砷酸钠在pSV2 gpt转化的CHO细胞系AS52中的黄嘌呤 - 鸟嘌呤磷酸核糖基转移酶位点(gpt)的致突变性。该化学物质在该位点诱导了突变频率的剂量依赖性增加。巢式PCR分析显示,大多数亚砷酸盐诱导的AS52突变体完全缺失了gpt基因。对于AS52细胞中的自发突变体、50μmol/L亚砷酸盐诱导的突变体和100μmol/L亚砷酸盐诱导的突变体,gpt基因完全缺失的百分比分别为36.00%、54.72%和66.67%。用直接DNA测序技术分析了来自9个100μmol/L亚硫酸氢钠诱导的突变体的gpt基因的PCR产物。在两个突变体(2/9)中鉴定出移码突变。在其他7个突变体中检测的结构基因中未发现基因组改变,其分子改变可能位于启动子区域。