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光复活作用可逆转紫外线辐射诱导的前诱变损伤,这种损伤会导致大肠杆菌发生移码突变。

Photoreactivation reverses ultraviolet radiation induced premutagenic lesions leading to frameshift mutations in Escherichia coli.

作者信息

Yamamoto K

出版信息

Mol Gen Genet. 1985;201(2):141-5. doi: 10.1007/BF00425650.

Abstract

The effect of photoreactivation of the ultraviolet radiation induced reversion of a trpE9777 frameshift mutation was studied in a uvr A6 derivative of Escherichia coli K12. Two different photoreactivation treatments were used, one providing a single flash of photoreactivating light and another providing 10 min of light from fluorescent lamps. The reversion frequency of the trpE9777 frameshift mutation was strongly reduced when subsequently exposed to visible light. The dose modification factor (the ratio of equally effective doses), for cells challenged with single-flash photoreactivation, for survival and induction of reversion to Trp+ was 3.6 and 3.4, respectively. UV induction of RecA protein synthesis was not reversed by a single flash of photoreactivation. The dose modification factor for 10 min of fluorescent lamp photoreactivation for survival and for induction of reversion to Trp+ was 6.5 and 6.3, respectively. The dose modification factor for 10 min of photoreactivation for induction of RecA protein was 1.7-2.5. Photoreactivation decreased the reversion of trpE9777 and increased survival to the same extent. We concluded that cyclobutyl pyrimidine dimers are the premutagenic lesions of UV mutagenesis of the trpE9777 allele in a uvr A6 background.

摘要

在大肠杆菌K12的uvr A6衍生物中,研究了紫外线诱导的trpE9777移码突变回复的光复活效应。使用了两种不同的光复活处理方法,一种是提供单次光复活闪光,另一种是提供10分钟的荧光灯光照。当随后暴露于可见光时,trpE9777移码突变的回复频率显著降低。对于接受单次闪光光复活处理的细胞,存活和诱导回复到Trp+的剂量修正因子(等效剂量之比)分别为3.6和3.4。单次闪光光复活不能逆转紫外线诱导的RecA蛋白合成。10分钟荧光灯光复活处理的存活和诱导回复到Trp+的剂量修正因子分别为6.5和6.3。10分钟光复活处理诱导RecA蛋白的剂量修正因子为1.7 - 2.5。光复活降低了trpE9777的回复频率,并在相同程度上提高了存活率。我们得出结论,在uvr A6背景下,环丁基嘧啶二聚体是trpE9777等位基因紫外线诱变的前诱变损伤。

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