Tlsty T D, Lieberman M W
Nucleic Acids Res. 1978 Sep;5(9):3261-73. doi: 10.1093/nar/5.9.3261.
The distribution of DNA repair synthesis in the chromatin of confluent human diploid fibroblasts damaged with N-acetoxy-2-acetylaminofluorene has been studied. Kinetic analysis of staphylococcal nuclease digestion data revealed that initially most of the repair synthesis occurred in nuclease sensitive regions of chromatin. Continuous labeling experiments and pulse chase experiments indicated that with time much of the 3H dThd initially incorporated into nuclease sensitive regions during repair appeared in nuclease resistant regions. Agarose gel electrophoresis was used to demonstrate that these resistant regions were core DNA. In agreement with previous findings [Smerdon, M.J. and Lieberman, M.W., (1978), Proc. Nat. Acad. Sci. USA, in press], studies of the time course of this rearrangement and of repair synthesis revealed similar time dependences and suggested a relationship between rates of repair synthesis and chromatin rearrangement.
对用N-乙酰氧基-2-乙酰氨基芴损伤的汇合人二倍体成纤维细胞染色质中的DNA修复合成分布进行了研究。对葡萄球菌核酸酶消化数据的动力学分析表明,最初大部分修复合成发生在染色质的核酸酶敏感区域。连续标记实验和脉冲追踪实验表明,随着时间的推移,最初在修复过程中掺入核酸酶敏感区域的大部分3H-dThd出现在核酸酶抗性区域。琼脂糖凝胶电泳用于证明这些抗性区域是核心DNA。与先前的研究结果一致[Smerdon, M.J.和Lieberman, M.W., (1978), Proc. Nat. Acad. Sci. USA,即将发表],对这种重排的时间进程和修复合成的研究揭示了相似的时间依赖性,并表明修复合成速率与染色质重排之间存在关系。