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紫外线诱导的SV40 DNA定向诱变

Targeted mutagenesis of SV40 DNA induced by UV light.

作者信息

Bourre F, Sarasin A

出版信息

Nature. 1983;305(5929):68-70. doi: 10.1038/305068a0.

Abstract

UV light is a potent mutagen in most living cells, but molecular analysis of its mode of action in animal cells has not been possible because of the high complexity of the cell genome. Therefore, we have used simian virus 40 (SV40) as a biological probe to study the mutagenic effect of UV-irradiation at the molecular level. A thermosensitive SV40 mutant of the large T antigen (tsA58), which is defective at high temperature for initiation of viral DNA replication and for repression of early transcription, was UV-irradiated in vitro, then replicated in monkey kidney cells. Revertants of tsA58 were selected for growth at the nonpermissive temperature, then the reversion sites were mapped by using the marker rescue technique, and precisely localized by DNA sequencing. We report here that all revertants analysed showed one or two base pair substitutions localized in the C-terminal half of the T antigen gene. The original tsA58 mutation was still present in all revertant genomes. In 16 DNAs sequenced, seven reversion sites were found on the large T antigen gene, all of which localized opposite a possible UV-induced pyrimidine-pyrimidine lesion, suggesting targeted mutagenesis. UV-irradiation of the host cell before infection did not change the pattern of reversion sites at the molecular level, although it strongly increased the mutation frequency. These results demonstrate for the first time in animal cells the specificity of UV-induced mutagenesis.

摘要

紫外线在大多数活细胞中是一种强大的诱变剂,但由于细胞基因组高度复杂,对其在动物细胞中的作用模式进行分子分析一直无法实现。因此,我们使用猴病毒40(SV40)作为生物探针,在分子水平上研究紫外线照射的诱变效应。对大T抗原的一种温度敏感型SV40突变体(tsA58)进行体外紫外线照射,该突变体在高温下启动病毒DNA复制和抑制早期转录存在缺陷,然后在猴肾细胞中进行复制。选择tsA58的回复突变体在非允许温度下生长,然后使用标记拯救技术对回复突变位点进行定位,并通过DNA测序精确确定其位置。我们在此报告,所有分析的回复突变体均显示在T抗原基因的C端一半区域存在一个或两个碱基对替换。原始的tsA58突变仍存在于所有回复突变体基因组中。在16个测序的DNA中,在大T抗原基因上发现了7个回复突变位点,所有这些位点都位于一个可能的紫外线诱导的嘧啶 - 嘧啶损伤对面,表明存在靶向诱变。感染前对宿主细胞进行紫外线照射,虽然强烈增加了突变频率,但在分子水平上并未改变回复突变位点的模式。这些结果首次在动物细胞中证明了紫外线诱导诱变的特异性。

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