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人细胞DNA-核基质复合物中DNA修复补丁分布的分析。

Analysis of the distribution of DNA repair patches in the DNA-nuclear matrix complex from human cells.

作者信息

Mullenders L H, Van Zeeland A A, Natarajan A T

出版信息

Biochim Biophys Acta. 1983 Sep 9;740(4):428-35. doi: 10.1016/0167-4781(83)90091-x.

Abstract

The distribution of ultraviolet-induced repair patches along DNA loops attached to the nuclear matrix, was investigated by digestion with DNA-degrading enzymes and neutral sucrose gradient centrifugation. When DNA was gradually removed by DNAase 1, pulse label incorporated by ultraviolet-irradiated cells during 10 min in the presence of hydroxyurea or hydroxyurea/arabinosylcytosine showed similar degradation kinetics as prelabelled DNA. No preferential association of pulse label with the nuclear matrix was observed, neither within 30 min nor 13 h after irradiation. When the pulse label was incorporated by replicative synthesis under the same conditions, a preferential association of newly-synthesized DNA with the nuclear matrix was observed. Single-strand specific digestion with nuclease S1 of nuclear lysates from ultraviolet-irradiated cells, pulse labelled in the presence of hydroxyurea/arabinosylcytosine, caused a release of about 70% of the prelabelled DNA and 90% of the pulse-labelled DNA from the rapidly sedimenting material in sucrose gradients. The results suggest no specific involvement of the nuclear matrix in repair synthesis, a random distribution of repair patches along the DNA loops, and simultaneously multiple incision events per DNA loop.

摘要

通过用DNA降解酶消化和中性蔗糖梯度离心,研究了紫外线诱导的修复斑块沿附着于核基质的DNA环的分布情况。当用DNA酶1逐渐去除DNA时,在羟基脲或羟基脲/阿糖胞苷存在下,紫外线照射细胞在10分钟内掺入的脉冲标记显示出与预标记DNA相似的降解动力学。在照射后30分钟内或13小时内,均未观察到脉冲标记与核基质的优先结合。当在相同条件下通过复制合成掺入脉冲标记时,观察到新合成的DNA与核基质的优先结合。用核酸酶S1对在羟基脲/阿糖胞苷存在下进行脉冲标记的紫外线照射细胞的核裂解物进行单链特异性消化,导致约70%的预标记DNA和90%的脉冲标记DNA从蔗糖梯度中快速沉降的物质中释放出来。结果表明,核基质不参与修复合成,修复斑块沿DNA环随机分布,并且每个DNA环同时发生多个切口事件。

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