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一种用于鉴定裂殖酵母粟酒裂殖酵母中自发突变和辐射诱导突变的新型穿梭载体系统。

A new shuttle vector system for the identification of spontaneous and radiation-induced mutations in the fission yeast Schizosaccharomyces pombe.

作者信息

Zhao Y, Goriparthi L, Lieberman H B

机构信息

Department of Radiation Oncology, College of Physicians and Surgeons, Columbia University, New York, NY 10032.

出版信息

Mutat Res. 1994 Nov 1;311(1):111-23. doi: 10.1016/0027-5107(94)90079-5.

Abstract

A shuttle vector, pCRR1, has been constructed for the detection of spontaneous and radiation-induced mutations in the fission yeast Schizosaccharomyces pombe. This vector contains an Escherichia coli supF suppressor tRNA gene as the target for mutagenesis and bacterial pMB1 and yeast ars1 replication origins, which can be used to propagate the plasmid in bacterial and fission yeast cells, respectively. supF mutations can be detected after plasmid transformation into S. pombe and recovery in a bacterial indicator system, KS40/pKY241, by selecting for nalidixic acid resistance and/or by screening for lacZ- cells. We found that UV light or gamma-rays induced mutations in a dose-dependent manner in this system. Treatment of ultraviolet light (UV)-irradiated DNA with E. coli photolyase, which monomerizes cyclobutane pyrimidine dimers, before introduction into S. pombe reduced mutation frequencies to nearly background levels, indicating that this type of lesion is the major source of mutations. Comparison of spontaneous and UV-induced mutation frequencies in rad+, rad8-190 and rad13-A cells revealed no significant difference in background levels or induced levels after exposure to 100 J/m2 of UV. However, when plasmid DNA was UV-irradiated with 500 J/m2, the rad8-190 cells generated only 38% as many induced supF mutations as the rad+ strain, whereas the rad13-A cells produced more than a 6-fold increase in mutability relative to the level observed for the wild-type strain. These mutability patterns are consistent with previous studies that characterized rad8-190 cells as hypomutable and rad13-A cells as hypermutable by UV light at chromosomal loci. Thus, this shuttle vector system provides a useful and sensitive tool to assess mutability in S. pombe.

摘要

已构建了一种穿梭载体pCRR1,用于检测裂殖酵母粟酒裂殖酵母中的自发突变和辐射诱导突变。该载体包含一个大肠杆菌supF抑制性tRNA基因作为诱变靶点,以及细菌pMB1和酵母ars1复制起点,它们可分别用于在细菌和裂殖酵母细胞中扩增质粒。将质粒转化到粟酒裂殖酵母中并在细菌指示系统KS40/pKY241中回收后,通过选择对萘啶酸的抗性和/或筛选lacZ-细胞,可以检测到supF突变。我们发现,在该系统中,紫外线或γ射线以剂量依赖的方式诱导突变。在将紫外线(UV)照射的DNA导入粟酒裂殖酵母之前,用可使环丁烷嘧啶二聚体单体化的大肠杆菌光解酶处理,可将突变频率降低至接近背景水平,这表明此类损伤是突变的主要来源。比较rad+、rad8-190和rad13-A细胞中的自发突变频率和紫外线诱导的突变频率,发现在暴露于100 J/m2紫外线后,背景水平或诱导水平没有显著差异。然而,当质粒DNA用500 J/m2紫外线照射时,rad8-190细胞产生的诱导supF突变仅为rad+菌株的38%,而rad13-A细胞的突变率相对于野生型菌株观察到的水平增加了6倍以上。这些突变模式与之前的研究一致,之前的研究将rad8-190细胞在染色体位点上的紫外线诱导下的突变能力表征为低变,而rad13-A细胞为高变。因此,这种穿梭载体系统为评估粟酒裂殖酵母中的突变能力提供了一种有用且灵敏的工具。

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