Oller A R, Thilly W G
Division of Toxicology, Massachusetts Institute of Technology, Cambridge 02139.
J Mol Biol. 1992 Dec 5;228(3):813-26. doi: 10.1016/0022-2836(92)90866-i.
To test the hypothesis that reactive species in the oxygen cascade are responsible for spontaneous mutation, we examined the spectra of oxygen and hydrogen peroxide-induced mutations at the hprt locus in a human B-lymphoblastoid cell line. We compared these spectra with the spontaneous mutational spectrum. Large gene alterations were studied by Southern analysis of individual TGR clones. A combination of high fidelity polymerase chain reaction, denaturing gradient gel electrophoresis and direct DNA sequencing were used to detect and identify point mutations in exon 3 of hprt. With regard to spontaneous mutations, a previous study showed that 39% of the spontaneous TGR clones had large gene alterations. In the present study, the analysis of spontaneous point mutations within exon 3 revealed two hotspots. A one base-pair deletion (-A) at base-pair 256 or 257 and a two base-pair deletion (-GG) at base-pair 237 and 238, were detected in triplicate cultures. Each of the hotspots comprised about 1% of the TGR mutants. The analysis of individual oxygen-induced TGR clones (48 h, 910 microM-O2) showed 43% had large gene alterations similar to the spontaneous TGR clones. However, none of the spontaneous point mutation hotspots was found among triplicate oxygen-treated cultures. Two point mutations in common with H2O2-treated cultures were found in one of the three oxygen-treated cultures. Hydrogen peroxide-induced mutations (1 h, 20 microM) also differed from spontaneous mutations. Only 24% of the hydrogen peroxide-induced TGR clones had large gene alterations. The analysis of point mutations showed three hotspots within exon 3 of hprt. An AT to TA transversion at base-pair 259 had an average frequency of 3% of all TGR mutants (present in all of 3 H2O2-treated cultures). Two GC to CG transversions at base-pairs 243 and 202 were present at a frequency of 0.6% and 0.4%, respectively. A five base-pair deletion (base-pair 274 to 278) was present at an average frequency of 0.3%. The latter three mutations were detected in two of three H2O2-treated cultures. Thus, the point mutation spectra of both oxygen and hydrogen peroxide were significantly different from the spontaneous spectrum. The oxygen and hydrogen peroxide-induced spectra shared some features, suggesting that oxygen and hydrogen peroxide share some but not all pathways for induction of mutations within the DNA sequence studied here.(ABSTRACT TRUNCATED AT 400 WORDS)
为了验证氧级联反应中的活性物质是自发突变的原因这一假设,我们检测了人B淋巴母细胞系中次黄嘌呤磷酸核糖转移酶(hprt)基因座处氧和过氧化氢诱导的突变谱。我们将这些谱与自发突变谱进行了比较。通过对单个TGR克隆进行Southern分析来研究大的基因改变。采用高保真聚合酶链反应、变性梯度凝胶电泳和直接DNA测序相结合的方法来检测和鉴定hprt第3外显子中的点突变。关于自发突变,先前的一项研究表明,39%的自发TGR克隆存在大的基因改变。在本研究中,对第3外显子内自发点突变的分析揭示了两个热点。在一式三份培养物中检测到第256或257碱基对处的一个碱基对缺失(-A)以及第237和238碱基对处的两个碱基对缺失(-GG)。每个热点约占TGR突变体的1%。对单个氧诱导的TGR克隆(48小时,910微摩尔/升-O2)的分析表明,43%存在与自发TGR克隆类似的大的基因改变。然而,在一式三份经氧处理的培养物中未发现任何自发点突变热点。在三份经氧处理的培养物中的一份中发现了与经过氧化氢处理的培养物共有的两个点突变。过氧化氢诱导的突变(1小时,20微摩尔)也与自发突变不同。只有24%的过氧化氢诱导的TGR克隆存在大的基因改变。点突变分析显示hprt第3外显子内有三个热点。第259碱基对处的AT到TA颠换在所有TGR突变体中的平均频率为3%(存在于所有三份经过氧化氢处理的培养物中)。第243和202碱基对处的两个GC到CG颠换的频率分别为0.6%和0.4%。一个五个碱基对的缺失(第274到278碱基对)的平均频率为0.3%。后三个突变在三份经过氧化氢处理的培养物中的两份中被检测到。因此,氧和过氧化氢诱导的点突变谱与自发谱显著不同。氧和过氧化氢诱导的谱有一些共同特征,表明氧和过氧化氢在本文研究的DNA序列内诱导突变的途径有一些相同但并非全部相同。(摘要截断于第400个单词)