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紫外线诱导的DNA修复在人VA13细胞中的核内定位。

Intranuclear localization of UV-induced DNA repair in human VA13 cells.

作者信息

Harless J, Hewitt R R

出版信息

Mutat Res. 1987 Mar;183(2):177-84. doi: 10.1016/0167-8817(87)90060-5.

Abstract

We have investigated the intranuclear localization of DNA-repair synthesis in G1-phase VA13 human cells. Ultraviolet-irradiated cells were permitted to perform unscheduled DNA synthesis in 3H-thymidine (3H-TdR) and then extracted with nonionic detergent and 2 M NaCl to produce nucleoids in which residual nuclear matrix was surrounded by an extended halo of DNA loops. Autoradiographic analysis of these structures permitted discrimination of DNA repair between the matrix and halo regions. Repair label in nucleoids prepared from cells after exposure to fluences of 2.5-30 J/m2 exhibited a dose-dependent association with the nuclear matrix, which ranged from 80% after 2.5 J/m2 to 50% after 30 J/m2. These results support the view that DNA repair is a nuclear matrix-associated process. This conclusion is in agreement with our preliminary study (Harless et al., 1983) and the results of McCready and Cook (1984) but contrasts with that of Mullenders et al. (1983). Questions concerning the differing experimental designs and their potential effects on the localization of DNA repair are discussed. The implications of these results to previous attempts to isolate chromatin factors associated with DNA repair are also considered.

摘要

我们研究了G1期VA13人细胞中DNA修复合成的核内定位。用紫外线照射细胞,使其在3H-胸腺嘧啶核苷(3H-TdR)中进行非预定DNA合成,然后用非离子去污剂和2M NaCl提取,以产生核小体,其中残余的核基质被DNA环的延伸晕圈包围。对这些结构进行放射自显影分析,可以区分基质区域和晕圈区域的DNA修复。从暴露于2.5 - 30 J/m2通量的细胞制备的核小体中的修复标记显示出与核基质的剂量依赖性关联,范围从2.5 J/m2后的80%到30 J/m2后的50%。这些结果支持DNA修复是一个与核基质相关的过程这一观点。这一结论与我们的初步研究(哈勒斯等人,1983年)以及麦克里迪和库克(1984年)的结果一致,但与穆伦德斯等人(1983年)的结果相反。讨论了关于不同实验设计及其对DNA修复定位的潜在影响的问题。还考虑了这些结果对先前分离与DNA修复相关的染色质因子的尝试的影响。

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