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[插入质粒DNA中的质粒基因和染色体基因的诱导诱变。I. 辐射的诱变作用]

[Induced mutagenesis of plasmid and chromosomal genes inserted into plasmid DNA. I. The mutagenic action of radiation].

作者信息

Esipova V V, Vedunova S L, Kriviskiĭ A S

出版信息

Genetika. 1984 Apr;20(4):533-41.

PMID:6373497
Abstract

This paper describes the results of treating plasmid DNA in vitro with mutagens, to obtain mutations both in plasmid genes and chromosomal genes comprised within the plasmid, thus avoiding disorganization characteristic of in vivo mutagenesis. The model system is represented by DNA of RSF2124 responsible for colicine E1 synthesis and resistance to ampicillin. Col- mutants were looked for after exposure to UV- and gamma-irradiation. The lethal effect was estimated as inactivation of the ampicillin resistance marker. After reisolation from mutant transformant of the plasmid DNA, the novel character and resistance to ampicillin proved to retain in the course of subsequent transformations and passages of transformed colonies, suggesting the mutational nature of the changes. Exposure of RSF2124 to short-wave UV-irradiation (lambda = 254 nm) produced a pronounced mutagenic effect: the relative quantity of Col- mutants under optimal conditions of mutagenesis increased about 10 times. In the case of W-reactivation (additional UV-irradiation of C600 wild type cells) of lethal lesions, a 95% reliable increase in mutagenic effect was observed. Significant enhancement of mutagenesis (about 4-fold) was detected when only recipient cells were exposed to low doses of UV (the so-called indirect UV mutagenesis). Thus, with regard to W- and indirect UV mutagenesis, the plasmid DNA behaves like DNA of temperate phages which suggests their evolutionary relationship. Treatment of plasmid DNA with acridine orange prior to UV, only protected from lethal lesions. Gamma-irradiation (60Co) at the dose producing 100-fold inactivation, increased the yield of Col- mutants by one order of magnitude. The presence of RSF2124 plasmid in a cell does not affect its UV sensitivity.

摘要

本文描述了用诱变剂体外处理质粒DNA的结果,以在质粒基因和质粒所含的染色体基因中获得突变,从而避免体内诱变的无序性。该模型系统由负责大肠杆菌素E1合成和氨苄青霉素抗性的RSF2124 DNA代表。在暴露于紫外线和γ射线照射后寻找Col-突变体。致死效应通过氨苄青霉素抗性标记的失活来估计。从质粒DNA的突变转化体中重新分离后,新特性和对氨苄青霉素的抗性在随后的转化和转化菌落传代过程中得以保留,表明这些变化具有突变性质。将RSF2124暴露于短波紫外线照射(λ = 254 nm)产生了明显的诱变效应:在最佳诱变条件下Col-突变体的相对数量增加了约10倍。在对致死损伤进行W-复活(对C600野生型细胞进行额外的紫外线照射)的情况下,观察到诱变效应有95%的可靠增加。当仅受体细胞暴露于低剂量紫外线(所谓的间接紫外线诱变)时,检测到诱变作用显著增强(约4倍)。因此,就W-和间接紫外线诱变而言,质粒DNA的行为类似于温和噬菌体的DNA,这表明它们之间存在进化关系。在紫外线照射前用吖啶橙处理质粒DNA,仅能防止致死损伤。剂量为产生100倍失活的γ射线照射(60Co)使Col-突变体的产量增加了一个数量级。细胞中RSF2124质粒的存在不影响其对紫外线的敏感性。

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