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酵母中8-甲氧基补骨脂素光诱导交联的修复。通过碱性逐步洗脱和电子显微镜分析。

Repair of 8-methoxypsoralen photoinduced cross-links in yeast. Analysis by alkaline step-elution and electron microscopy.

作者信息

Cundari E, Dardalhon M, Rousset S, Averbeck D

机构信息

Istituto di Mutagenesi e Differenziamento C.N.R., Pisa, Italy.

出版信息

Mol Gen Genet. 1991 Sep;228(3):335-44. doi: 10.1007/BF00260625.

Abstract

The repair of interstrand cross-links induced by 8-methoxypsoralen plus UVA (365 nm) radiation DNA was analyzed in diploid strains of the yeast Saccharomyces cerevisiae. The strains employed were the wild-type D7 and derivatives homozygous for the rad18-1 or the rad3-12 mutation. Alkaline step-elution and electron microscopy were performed to follow the process of induction and removal of photoinduced cross-links. In accordance with previous reports, the D7 rad3-12 strain failed to remove the induced lesions and could not incise cross-links. The strain D7 rad18-1 was nearly as efficient in the removal of 8-MOP photoadducts after 2 h of post-treatment incubation as the D7 RAD+ wild-type strain. However, as demonstrated by alkaline step-elution and electron microscopic analysis, the first incision step at DNA cross-links was three times more effective in D7 rad18-1 than in D7 RAD+. This is consistent with the hypothesis that the RAD18 gene product is involved in the filling of gaps resulting from persistent non-informational DNA lesions generated by the endonucleolytic processing of DNA cross-links. Absence of this gene product may lead to extensive strand breakage and decreased recognition of such lesions by structural repair systems.

摘要

在酿酒酵母的二倍体菌株中,分析了8-甲氧基补骨脂素加UVA(365nm)辐射DNA诱导的链间交联的修复情况。所用菌株为野生型D7以及rad18 - 1或rad3 - 12突变纯合的衍生物。进行了碱性逐步洗脱和电子显微镜观察,以跟踪光诱导交联的诱导和去除过程。与先前的报道一致,D7 rad3 - 12菌株无法去除诱导的损伤,也无法切割交联。D7 rad18 - 1菌株在处理后孵育2小时后去除8 - MOP光加合物的效率几乎与D7 RAD +野生型菌株相同。然而,正如碱性逐步洗脱和电子显微镜分析所表明的,D7 rad18 - 1中DNA交联处的首次切割步骤比D7 RAD +有效三倍。这与以下假设一致,即RAD18基因产物参与填充由DNA交联的核酸内切酶加工产生的持续性非信息性DNA损伤所导致的缺口。该基因产物的缺失可能导致广泛的链断裂,并降低结构修复系统对这类损伤的识别。

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