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[同步化中国仓鼠细胞中基因突变的诱导及紫外线的致死作用]

[Induction of gene mutations and the lethal action of ultraviolet rays in synchronized Chinese hamster cells].

作者信息

Manuilova E S

出版信息

Genetika. 1977;13(1):37-45.

PMID:612481
Abstract

Lethal and mutagenic effects of UV light were studied in two synchronized UV-sensitive Chinese hamster cell clones differing in the degree of sensitivity (CHS1, CHS2). It is shown that the phase of mitosis is most resistant to the lethal effect of UV. The sensitivity of both cell clones increases in the pre-synthetic phase and reaches its maximum during the phase of DNA synthesis. Positive correlation of cell sensitivity to mutagenic and lethal action of UV was observed when studying induced mutability in both cell clones during the phase of DNA synthesis. However, the study of the mutagenic effect of UV on different phases of the synthesis. However, the study of the mutagenic effect of UV on different phases of the cell cycle (M, G1, S) in the less UV-sensitive cell clone has revealed that the maximal mutation yield takes place when cells are irradiated at G1 (CHS1). The discrepancy observed may be due to different probability of the phenotypic detection of pre-mutational lesions, arising at different phases of the cell cycle. It is shown that only one cell generation is necessary for the expression of pre-mutational changes. These data allow to conclude that the increased mutation rate observed at G1 (as compared with S) reveals rather a probability of the expression but not of the occurrence of pre-mutational lesions. It is suggested that the fixation of mutations in the cells studied proceeds during the post-replication repair synthesis.

摘要

在两个对紫外线敏感程度不同的同步化中国仓鼠细胞克隆(CHS1、CHS2)中研究了紫外线的致死和诱变效应。结果表明,有丝分裂期对紫外线的致死效应最具抗性。两个细胞克隆在合成前期的敏感性增加,并在DNA合成期达到最大值。在研究DNA合成期两个细胞克隆的诱导突变性时,观察到细胞对紫外线诱变和致死作用的敏感性呈正相关。然而,对紫外线在合成不同阶段诱变效应的研究。然而,对紫外线在紫外线敏感性较低的细胞克隆细胞周期不同阶段(M、G1、S)的诱变效应研究表明,当细胞在G1期(CHS1)受到照射时,突变产量最高。观察到的差异可能是由于在细胞周期不同阶段产生的突变前损伤的表型检测概率不同。结果表明,突变前变化的表达仅需一个细胞世代。这些数据表明,在G1期观察到的突变率增加(与S期相比)反映的是突变前损伤表达的概率,而非其发生的概率。有人提出,所研究细胞中的突变固定发生在复制后修复合成过程中。

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