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体外培养的p388f淋巴瘤细胞经甲基硝基亚硝基胍(MNNG)处理后DNA修复的时间进程。II. DNA修复合成及其与链断裂的相关性。

The time course of DNA repair following methyl nitro-nitrosoguanidine (MNNG) treatment of p388f lymphoma cells in culture. II. DNA repair synthesis and its correlation with strand breakage.

作者信息

Nikaido O, Fox B W

出版信息

Chem Biol Interact. 1976 Jul;14(1-2):47-55. doi: 10.1016/0009-2797(76)90023-5.

Abstract

Repair synthesis has been followed in P388F cell DNA following treatment with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) using 5-iodo-deoxyuridine (IUdR) and [3H] thymidine combination. A pattern of repair synthesis was obtained, similar in its timing to the initial and medial stages of single-strand break formation and rejoining within the first 24 h after treatment. A higher base insertion frequency in relation to single-strand breaks occurs during the medial stage of repair. However, a fundamental problem with the use of iododeoxyuridine and [3H] thymidine ([3H] TdR) as a suitable measure of repair synthesis was encountered and a potential source of error in such experiments was observed.

摘要

使用5-碘脱氧尿苷(IUdR)和[3H]胸苷组合,在经N-甲基-N'-硝基-N-亚硝基胍(MNNG)处理的P388F细胞DNA中追踪修复合成。获得了一种修复合成模式,其时间与处理后最初24小时内单链断裂形成和重新连接的初始和中间阶段相似。在修复的中间阶段,相对于单链断裂出现了更高的碱基插入频率。然而,遇到了使用碘脱氧尿苷和[3H]胸苷([3H] TdR)作为修复合成合适测量方法的一个基本问题,并观察到此类实验中一个潜在的误差来源。

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